BIOL112- cell structure and function Flashcards

(365 cards)

1
Q

what is a cell

A

simplest component in biology which is alive

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2
Q

what is every living organism composed of

A

eukaryotic cells
or
prokaryotic cells

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3
Q

which domain is the most diverse

A

bacteria

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4
Q

what is eukaryotic most closely related to

A

archea domain

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5
Q

descibe prokaryotic cells

A

Prokaryotic cells developed 3.5 billion years ago.​

Prokaryotic cells are the most abundant type on earth today​

Collective biomass of prokaryotic cells on the world is 10
times that of eukaryotes​

Prokaryotic cells are simple in structure but biochemically
diverse​

Prokaryotic cells do not have a membrane bound nucleus​

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6
Q

where did eukaryotic cells develop from

A

from prokaryotic cells arond 2 billion years ago

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7
Q

what are prokaryotic cells divided into

A

bacteria and archaea

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8
Q

what size is bacteria

A

1-2 micrpns

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9
Q

what size are viruses

A

20-200 nanometers

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10
Q

what size are eukaryotic cells

A

10-100 microns

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11
Q

what are extermophiles

A

live in extreme environment such as hot springs and antartica
they are adapted to specific types of environemnts and have adaptations to live in these ectreme environements

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12
Q

examples of how extremophiles adapt to environemnts

A

Thermals stable enzymes and proteins that fold in a way to protect from the heat . Different plasma membrane consituencies, derive their energy differently.​

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13
Q

names of specific extermophiles on lec 1 slide 17

A
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14
Q

what are the biotechniqal applications for extremophiles

A

Polymerase Chain Reaction​

Biofuels​

Biomining​

Carotenoid production​

Detergents​

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15
Q

why is peptidoglycans presents in bacteria useful

A

its only present in bacteria so can be a good taget fro drugs

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16
Q

bacteria, archaea and eukarya
nuclear envelope?

A

eukarya

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17
Q

bacteria, archaea and eukarya
membrane enclosed organelles ?

A

eukarya

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18
Q

bacteria, archaea and eukarya
peptidoglycan in cell wall

A

bacteria

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19
Q

bacteria, archaea and eukarya
membrane lipids, what is the branching

A

bacteria - unbranched hydrocarbons
archaea- some branched hydrocarbons
eukarya- unbranched hydrocarbons

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20
Q

bacteria, archaea and eukarya
rna polymerase

A

bacterua - one kind
arcgaea + eukarya = several

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21
Q

bacteria, archaea and eukarya
introns in genes

A

bacteria - rare
archaea- some
eukaeya- many

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22
Q

bacteria, archaea and eukarya
histones

A

bacteria- absent
archaea- some
eukaraya- present

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23
Q

bacteria, archaea and eukarya
cirucular chromosomes

A

bacteria and archaea

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24
Q

bacteria, archaea and eukarya
what is the initiator aminoa cid for protein synthesis

A

bacteria- formyl methionine
archaea+ eukarya- methionine

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25
descibe prokaryotic cell structures
Plasma membrane very simlar in terms of compositon to eukaryotes ​ Cell wall – peptidoglycan ​ Capsule – protects from attacks from the immune system, aslo can cause an immune response If recognised​ Flagellum- how they move​ Pilli- hair like structues, involved in sticking to substrated and in comunication ​
26
components of prokaryotic cells
Nucleoid region: contains circular DNA, no nuclear membrane​ ​ Plasma membrane: has the same basic structure of all biological membranes.​ ​ Some prokaryotes have infoldings of the plasma membrane which contain specialized enzymes. ​ ​ The cytoplasm contains ribosomes and little else.​ Many prokaryotes have a cell wall​ Some prokaryotes have flagella composed of the protein Flagellin. ​ Pili are composed of the protein Pilin and help bacterial stick to their substrate or to each other​ Many bacteria also secret a Capsule usually of polysaccharides​ Bacteria have a diverse range of shapes the most common being Cocci (spherical),bacilli (rod shaped), and spirochetes (helical). ​
27
what is it called when pili exchange stuff
conjugation
28
descibe the prokaryotic cell wall
protects the cell from osmotic shocks composed of peptidoglyca
29
what 2 types of bacteria cell walls are there
gram positive gram negative
30
describe gram positive
think simple single layer no lipopolysaccahrides there are teichoic acids pruple gram stain susceptible to antibiotic resistance so easier to treat
31
descibe gram negative
thin, complex double layer no teichoic acids there are lipopolysacchardies pink gram stain resistant to antibiotic resistance
32
uses of bacteria in medical ( biotechnology )
Bacteria can be used to produce large quantities of proteins cheaply for therapeutic use for example Insulin.​ Drug screening tests and diagnostics.​ ​
33
uses of bacteria in agriculture
Introduction of a new gene in plant chromosome​ Example - purple tomatoes have high anthocyanin​
34
uses of bacteria in environmental biotechnology
Bioremediation – removes pollutants, industrial by-products, oil spills
35
uses of bacteria in industry
Lactic bacteria develop the flavour and colour of foodstuff​ Improve the storage longevity of wines​
36
is metabolic diveristy greater under prokaryotes or eukaryotes
prokaryotes
37
what is an autotroph
producers – make their own food – plants, algae, bacteria​
38
what is a heterotroph
Consumers – consume producers/consumers – mammals​ ​
39
what does photo mean
uses light
40
what does chemo mean
uses molecules or compounds
41
........ are photoautotrophs and chemoheterotrophs
eukaryotes
42
....... Chemoautotrophs, Chemoheterotrophs, Photoautotrophs, photoheterotrophs.​
prokaryotes
43
descibe viruses
Are they alive?​ They cannot self repair​ No energy transduction system​ Only visible with the electron microscope​ Each complete viral particle is called a virion​ Protein coat is termed the capsid, which is made up of protein units called capsomers​ they are not prokaryotes or eukaryotes
44
desicbe eilamentous vrius
The nucleic acid is arranged in a helix, with the protein sub-units surrounding and stabilizing it. An example is Tobacco mosaic virus
45
descibe spheroid virus
The nucleic acid is condensed inside a protein envelope which is usually organized into a multisided geometric shape. An example are adenovirus different types cause illness ranging from Gastroenteritis to keratoconjunctivitis
46
descibe enveloped virus
Have lipid envelopes includes the influenza and coronaviruses viruses​ ​
47
describe tailed spheroid virus
This is basically a spheroid virus with a tail. An example is the lambda phage
48
describe the development of cell biology ( with reference to microscopes )
The foundations of cell biology were formed in the 17th century. ​ In 1665 Robert Hooke published a collection of essays under the title Micrographica. One essay gave a detailed description of a section of cork, in which Hooke described seeing a honeycomb of chambers- now what we call cells. ​ ​ In 1675 Dutchman Anton Van Leeuwenhoek had improved the art of polishing lenses. Leeuwenhoek's best microscopes were able to resolve to about 1.5 microns. He was able to report what he described as a host of little animals in a drop of rain water, these turned out to be protozoa. Leeuwenhoek was later on to describe the existence of bacteria. ​ ​ ​ In the 19th century the maximum theoretical resolution of the light microscope was attained (approximately 0.25 microns).​ ​ In the 1930's the electron microscope was developed allowing cell organelles to be seen. The term ultrastructure was coined to describe the level of detail obtainable with the EM. ​ ​ ​
49
what is magnification
the ratio of an objects image size to its real size
50
what is resolution
the measure of the minimum distance of 2 ditinguishable points
51
what is contrast
visible differences in brightness or colour between parts of the sample
52
what are the 2 types of light microscopes
dissecting compound brightfield
53
descibe a dissecting microscope
see structral features 70x magnification reflect light so you can see sample
54
descibe compound brightfield microscopes
in depth features, 40-1000x magnification light passes through stage through a series of objector lenses magnification = ocular x objector
55
what is the most common ligth microscope and what must the sample be
bright field the light passes through the specimen so must be at least pertially transparent
56
advantage of light microscopes
image living cell s
57
name some other major types of LM
fluorescent, phase/differential contrast and confocal microscopes.​
58
dissadvantage of light microscopes
limited resolution ( o.2 microns)
59
whats one way to improve the resoltuion of a microscope
shorter wavelneght of radiation
60
how do you prep a sample for light microscopy and what is the reason for each step
Whole mounts: small relatively transparent specimens can be mounted directly onto slides​ Tissue sections: most tissues need to be sectioned before they can be examined​ Fixation: This involves using chemical fixatives to prevent cell autolysis and to preserve the structure of the tissue. ​ Dehydration and clearing: This removes the water from the tissue in preparation for wax impregnation​ Embedding: The specimen is infiltrated with molten wax, after which it is transferred to a mould​ Sectioning: Thin sections approximately 5 microns thick are cut ​ on a microtome, and collected onto a glass slides​ Staining: The wax is removed and the tissue stained with ​ a coloured dye such as Eosin (cytoplasm) or haematoxylin (nuclei)
61
phase contrast microscopy
enhances contrast in unstained cells by amplifiying variation in density wihtin specimen, especiilay useful for examining living unpigmented cells
62
differential - interference contrast
like phase contrast microscopy it uses optical modifications to exaggerate differnces in density
63
slide 19 lec 2 ??
64
descibe a flourescence microscope
shows the locations of specific molecules in the cell. flourescent substances absorb short-wavelengths uv radiation and emit long wavelength , visable light oftern made by tagging the moleucles of interest with flourescent moelcules
65
describe confocal microscope
uses lasers and special optics for optical sectoning , only those regions within a narrow depth of focus are imaged typically used with flouresemtly names samples 3d image can use fixed or live cells if we use live we can add how it chnages over time, so time can be added as a 4thdimention
66
what does deconvolution microscopy dp
Algorithms remove out of focus light and this sharpens the image and improves resolution.​
67
what does super resolution do
gathers light from individual fluorescent molecules and records their position. Combining information from these individual molecules breaks the resolution limit.​
68
why is the resolution of an electron microscope better than a light mciroscope
electrons have a very short wavelength so rosoultion 1000s of times better
69
why must electron microscopes be kept under vaccum
electrons have poor penetrating power
70
what can electrons be focused by
magnetic fields
71
what are the two main types of electron microscopes
transmission scanning
72
descibe a TEM
Electron gun: usually a heated tungsten filament which produces electrons by thermionic emission​ ​ Electron beam passes through the specimen​ ​ The image is focused and magnified by magnetic objective and projector lenses​ The electron image is converted into a visible image by a fluorescent screen, which is viewed through a glass window.​ Photographs can be taken using a digital camera​ ​ The whole inside of the microscope is kept at a high vacuum during operation​
73
list of TEM sample preparation
Whole mounts: Bacteria and viruses can be examined directly​ Tissue sections​ ​ Fixation: Usually in Glutaraldehyde (protein crosslinking) followed by a second fixation step in Osmium Tetroxide (lipid crosslinking)​ ​ Dehydration: In an ethanol series​ ​ Embedding: Specimens for TEM are embedded in plastic resins such as Epoxy resins. ​ ​ Sectioning: 50nm thick sections are cut using a ultramicrotome. ​ ​ Staining: Biological tissue has little contrast under the electron beam, so heavy metal stains such as lead are used to improve contrast​ ​
74
descibe an SEM
So called because the electron beam is scanned across the specimen. Used for looking at the surface of specimens​ The top part to the microscope is similar to a TEM​ Its called a Scanning Electron Microscope as the electron beam is Scanned across the surface of the specimen.​ Electrons are reflected from the surface of the specimen, collected by a electron detector and converted into an electronic signal which is displayed on a screen.​ The image on the SEM represents the topology of the sample. The great depth of focus of the SEM gives images a 3-D appearance​ ​
75
sem sample preparation
Biological samples must be fixed and dried before being examined in the SEM under vacuum​ Fixation: The same fixatives are used as with TEM preparation​ Dehydration: The water is replaced with Ethanol​ Critical Point Drying: This technique allows all of the ethanol to be removed from the sample in a way that minimises shrinkage​ Coating Specimens are coated with a thin layer of gold to protect them from electron beam damage
76
what is cell fractionation for
allows major organelles to be individuallt separateed out so they can be studied in isolaton
77
descibe cell fractionation
Cells are first homogenised to release the organelles.​ ​ Differential centrifugation isolates cell components on the basis of size and density by using increasing durations and g forces.​
78
uses of cell fractionation
Protein Enrichment Enrich target proteins and improve detection of low abundance protein Protein Characterization Identify the subcellular localization of a protein Protein Translocation Monitor translocation of cell signalling molecules from the cytoplasm to the nucleus
79
why are eukaryotics able to be larger than prokaryotic cells
because of their internal membrane system
80
descibe the basic features of eukaryotic cells
more comples genetic material is organized into chromosomes and enclosed in a nuclear envelope plasma membrane specialised organnelles inclusing numerous internal emembranes togther temred the endomemrbane system complex cytoskeleton plants have specialised structures inclusing chloroplasts , vaculose and a cell wall
81
descibe plant cell wall
maintains the cell shape and prevents mechanical damage. this cell wall is composed of cellulose fibres embedded in a protein/polysaccharide matric consisting mainly of hemicellulose and pectin
82
t or f plants dont have lysosomes or flagells
mostly true plants dont have lysosomes they dont normally have flagella
83
plasmodesmata
for comunucation between different plant cells / exchnage
84
endosymbiosis theory ??
lec 3 slide 10 who knows
85
describe nuclear memrbane
double membrane and contains nuclear pores about 100 nm in diameter.​
86
how is DNA in the nucleus organised
Within the nucleus DNA is organized (along with proteins called histones) into a material called chromatin. The nucleolus is where the components of ribosomes are manufactured.​ ​
87
what does chromatin condense into during cell divison
chromasomes
88
fucntions of the plasma membrane
​ Controls the entry of nutrients and the exit of waste products. Maintains the electrolyte balance in the cell. Acts as sensor to external signals​ ​
89
what were the 2 generations of the membrane model
lipid bilayrer sandwiched between 2 layers of proteins called the davson-daniellli model fluid mosaic model
90
what is glycocalyx
surrounds entire cell membrane and allows the immune system to detect self from foreign, this is unique to each person
91
mambranes lipids are ...... molecules what do they do in aqeuous environemnt
amphiphatic sponatiously form bilayers
92
is the lipid bilayer able to repair itself if damged
yes
93
what are the 3 main types of lipids in cell membranes
phosphlipids glycolipids cholesterol
94
describe the fluidity of membranes at... low temps and no cholesterol
PLa cluster togther low fluidity
95
describe the fluidity of membranes at... high temps no cholesterol
PLs more distnace high fluidity
96
describe the fluidity of membranes at... low temps and cholesterol
increases distance between PLs increases fluidity
97
describe the fluidity of membranes at... high temps cholesterol
decreases distance between PLs decreases fluidity
98
descibe transmembrane proteins
​ The polypeptide chain of membrane proteins often crosses the lipid bilayer several times, these are called trans membrane proteins.​ Transmembrane proteins are amphipathic they have hydrophobic regions and hydrophilic regions
99
describe peripheral proteins
Peripheral membrane proteins are only associated with the membrane by non-covalent linkages and are easily dislodged​ The shape and distribution of membrane proteins can be observed using freeze fracture electron microscopy.​ ​
100
descibe how freeze fracture electron microsppy supported th efluid mosaic model
Specialized preparation technique by flash-freezing the samples which splits the membrane along the middle of the phospholipid bilayer– Cryo Electron Microscopy the membrane breaks at the weakest points, which is right in the middle of the lipid tails so we can sperate it found that the insade was very different from the extracellular
101
how to carry out freeze fracture
Fixation and preservation with glycerol​ Rapid Freezing – liquid nitrogen​ Fracturing – under pressure using a liquid nitrogen cooled microtome​ Replication​ Replica cleaning​
102
evidance for drifting membrane proteins
mouse and human cell were fued to make a hybrid ell after 1 hour the proteins has mixed
103
what are some functions of membrane proteins
transport receptor sites structural roles cell junctions
104
desibe membrane proteins function fo r structural roles
membrane proteins called integrins, allow cell to attach to the extracellular matrix
105
descibe the membrane protein function for cell junctions
tight junctions are present between some cell types. They act to separate the apical and basal membranes which have different functions. ​
106
describe cystic fibrosis
Cystic fibrosis is caused by a defective chloride ion channel (a transmembrane protein). ​ This is an autosomal recessive disease.​ The failure of the chloride channel results in a build-up of viscous mucus within the lungs making the individual prone to infections.​ It appears to be an ideal disease to treat with gene therapy, but progress has been much slower than expected.​ ​
107
where is nearly all of the carbohydrates in plasma membrane and what mass can it account for
outer surface 10%
108
what are cell usrface carbohydrates known to be important in
cell-cell and cell to extracellular matrix recognition
109
whta are the ABO blood types determined by
carbohydrates on the surface of red blood cell s
110
example: how membrane glycoproteins such as HIV are involved in imunity
HIV must bind to the immune cell surface protein CD4 and a “co-receptor” CCR5 to infect a cell ​ HIV cannot enter the cells of resistant individuals that lack normal CCR5​
111
descibe epithelial tissue
sheets of tightly packet cells, covers the outside of the body and lines organs and cavities inside the body. eg. inner surface of the digestive track and respiratory track and outer surface of the body.
112
what are most epithelial cells fasterned togther via
desmosome junctions and sealed via tight junctions to withstand stresses and strains
113
functon of epithelium
protects against mechanical injury and also provides a barrier against mcirobed and fluid loss
114
t or f epithelium is one layer thick
f it can be, known as simple, but it also can be stratified ( several layers thivk)
115
role of conective tissue
mechanical strength binds and suports other tissues
116
what does connective tissue consist of
extracellular matrix , in which cells are sparsely scattered
117
dense connective tissue
such as cartilage bone and tendon has great mechanical strength and elasticity. Consists of just extracellular matrix with relatively few cells. Eg Bone Tendon, ligaments, sclera, cornea, cartilage.​ ​ Dense connective tissue is made up of :​ 1. Fibrous proteins (mainly collagen and elastin)​ 2. Ground substance usually proteoglycans ​ ​
118
loose connective tissue
Loose connective tissue holds small glands and epithelia together and includes the basal lamina of cells.​ ​ Blood and adipose tissue are also considered connective tissues although they don’t really fit very well into this category.​
119
where is loose connective tissue found
glands and organs to withstand stresses and strains
120
where is fibrous tissue found
around bones
121
where is adipose tissue found
supports tissue, function to support other tissue with energy
122
what is the role of muscle tissue
supprt movement
123
describe muscle tissue
long excitable cells , large number of actin and myosin filaments each fiber is further divided into myofibrils , which contain 2 types of filament Thin filaments composed of actin ​ Thick filaments composed of myosin​ ​ These two types of filaments slide past each other during contraction​ ​ The regular arrangement of the filaments along the myofibrils creates a banding pattern. Each band is termed a sarcomere.​ ​
124
what are the 3 muscle types and thier role
skeletal - volanatry movement smooth - involnatry body acitvities cardiac- contraction of the heart
125
what helps nourish, insulate and replenish neurons
glial or glia
126
what does a neuron consist of
cell body or soma 2 or ,ore nerve processes ( dendrites are processes, which coduct impulses away from the nerve body) Axons transmit impulses away from the nerve body.​ Specialised cells called Schwann cells wrap around an axon to form a multi- layered membrane sheath to provided electrical insulation.​ The signal is transmitted along the nerve cell in the form of ion fluxes across the plasma membrane of the cell​
127
do prokaryotes have an endomembrane system
no its unique to eukaryotes
128
what is the endomembrane system composed of
endoplasmic reticulum, golgi aparatus and lysosomes
129
descibe smooth ER
Most cell types have relatively little smooth ER (SER)​ ​ Phospholipid, fat and steroid (including sex hormones) manufacturer​ Carbohydrate metabolism​ Most cell types have relatively little smooth ER (SER)​ ​ Phospholipid, fat and steroid (including sex hormones) manufacturer​ Carbohydrate metabolism​
130
what does ser DO IN HEPATOCYTES
breaks down stored glycogen to release glucose
131
where is sacroplasmic reticulum found
muscle cells
132
what is the sarcoplasmic reticulum
network of tubular sacs, transmitts electrical signals, sequesters calcium ions from the cytosol
133
what does the level of intercellular calcium regulate
muscle contractions
134
what do mucles consist of
Muscles consist of myofibrils​ ​ Myofibrils are surrounded by sarcoplasmic reticulum​ ​ Myofibrils are composed of a repetitive arrangement of filaments called a sarcomere.
135
what is a sarcomere
a region where the myosin and actin filaments overlap
136
what happens when mucles cells reciebe action potentials from neuromusclular junctions through T tubules in the sarcoplasmic reticulum
salcoplasmic reticulum releases calcium ions, this binds to troponin causing a comformational change in tropomyosin myosin and actin can no interact
137
simple state what myosin actin z line h line a line i line is
Myosin – thick filaments​ Actin – thin filaments​ Z line – Sarcomere boundary and junction of actin and myosin filaments​ H line – Shortens during contraction and contains only myosin​ ​ A line – region containing length of asingle myosin filament. ​ ​ I line- region containing length of a single actin filament. ​
138
how do myosin actin interactions generate the force for muscle contractions
myosin head looses ATP, porviding energy for the head to nod puliing the actin across mysoin
139
what are the sites of 4 classes of protein sythesis
secreted glycosylated lysosomal enzymes membrane bound proteins
140
when can a ribosome become attached to an RER
Only ribosomes synthesizing proteins with a specific signal peptide sequence become attached to the RER​
141
describe proteins in the RER
The N-terminus of these proteins contains a signal peptide usually 20- 30 amino acids long. ​ A signal recognition particle (SRP) attaches to the signal peptide and stops translation in the cytosol​ The SRP docks to a SRP receptor on the ER membrane and translation starts again.​ The hydrophobic signal peptide passes through the membrane and loops back through the membrane and is cleaved off. The rest of the peptide passes through the membrane and into the ER lumen​ The signal sequence is cleaved off with the enzyme signal peptidase​
142
what does glycosylation in the RER mean
the additon of sugars or oligosaccharides
143
descibe glycoslyation in the RER
An oligosaccharide is added in the RER. It is composed of N- acetylglucosamine, mannose and glucose residues containing a total of 14 sugar residues is transferred to the proteins in the RER​
144
what does the golgi apparatus do
modifies and sorts the proteins which pass through it The Golgi complex also mediates the flow of proteins from the RER to various destinations within the endomembrane system.​ ​ The default pathway of proteins synthesized in the RER is through the Golgi and then to the plasma membrane for secretion.​
145
some proteins are tagged in golgi for specific destinations within the cell eg. lysomomal enzymes - exmplain how
Mannose residues of lysosome enzyme proteins are phosphorylated in the cis Golgi. ​ ​ A mannose 6-phosphate receptor then binds these proteins in the trans Golgi reticulum and directs their transfer to lysosomes​
146
when does glycosylation occur
as the protein pass through the golgi
147
what has impaired function in cystic fibrosis
cliated and goblet cells
148
describe lysosomes
Lysosomes are vesicular structures, limited by a single smooth membrane containing enzymes active at acid pHs​ ​ Lysosomes contain about 60 hydrolytic enzymes (manufactured in the RER) which will degrade almost all biomolecules. ​ ​
149
where do primary lysosomes origionate from
trans face of the golgi
150
what happens once a lysosomes fuses with its target
hydrogen ions are pumped into this secondary lysosomes to bring down the PH and active the enzyes
151
what do lysosomes carry out
​ Lysosomes carry out autophagy (recycling of worn out organelles)​ Lysosomes carry out phagocytosis eg destruction of bacteria by lymphocytes or feeding by amoeba​ Lysosomes carry out autolysis during apoptosi
152
describe lysosmal storage disease
Partially degraded insoluble metabolites can accumulate within lysosomes if a particular lysosomal enzymes is defective. ​ ​ The resulting material results in enlarged lysosomes that compromise cell function in over 50 different lysosomal storage diseases.​ ​ For example Tay - Sachs disease ​ ​ In Tay - Sachs disease – Hexosaminidase A enzyme deficiency results in the accumulation of the lipid ganglioside. ​ The clinical symptoms are due to accumulation of ganglioside in nerve cells. ​ Death usually occurs by 2-3 years of age ​ ​
153
describe exocytosis
Material is exported from the cell by Exocytosis​ ​ Exocytosis involves fusion of vesicles from the interior of the cell with the plasma membrane. The vesicles contents are then expelled into the surrounding medium.​ ​ Exocytosis is important in the secretion of numerous proteins including hormones, and extracellular structural proteins such as collagen and fluids such as mucus. ​
154
what is phagocytosis
uptake of insouble material
155
what is pinocytsosis
cells pinch thier PM to take up extracellular fluid inot small vensicles. non specific
156
what is receptor mediated endocytsosis
binding of macromolecules to specific cell surface receptros which triggers endocytosis
157
describe receptor mediated endocytosis
The macromolecules (such as transferrin which transports iron from the blood into cells) become concentrated in endocytic pits​ The endocytic pits are coated with a bristle-like protein called clathrin​ Clathrin polymerises around the vesicle forming a cage like structure​
158
what is the theory called for the mitrochondiral origin
endosymbiotic theory
159
descibe mitrochondria
All mitochondria have an inner and an outer membrane, with the inner membrane formed into cristae. There are two compartments in the mitochondria: the matrix inside the inner membrane and the inter-membrane space between the inner and outer membranes.​
160
how do mitrochondira change thier positions inside cells
mvoed by the microtubules of the cytoskeleton
161
where are mitrochondira oftern found
in regions of high ATP consumption, eg. in ht emyofibirls of muscle cells
162
descibe the mitrochondria outer membrane
similar to most other eukaryotes majore protein component is porin- large aqueous channels
163
descibe inner mitrochondiral membrnae
Contains three major types of membrane complexes:​ 1. Electron transport chain​ 2. ATP synthase​ 3. Specific transporters of metabolites which vary according to cell/tissue type​
164
descibe the cristae
increase membrane surface area​ energy transducing membrane​ impermeable to most small ions
165
descibe the mitrochondrial matric
enzymes which catalyse Krebs cycle and fatty acid oxidation​ ribosomes​ mitochondrial DNA ​
166
how is ATP the energy for cells
The reaction of ATP and water yields inorganic phosphate (Pi) and ADP and releases energy. Energy released by breakdown reactions (catabolism) in the cell is used to phosphorylate ADP, regenerating ATP. Chemical potential energy stored in ATP drives most cellular work.​
167
explain chemical work of ATP
Energy coupling using ATP hydrolysis. The exergonic process of ATP hydrolysis is used to drive an endergonic process.
168
explain mechnaical or trasport work of atp
Mechanical or transport: ATP hydrolysis causes changes in the shapes and binding affinities of proteins. This can occur either directly, by phosphorylation, for example for a membrane protein carrying out active transport of a solute, or indirectly, via noncovalent binding of ATP and its hydrolytic products, as is the case for motor proteins that move vesicles (a type of organelle) along cytoskeletal “tracks” in the cell​
169
Mitochondria are able to use........derived from organic molecules​ Electrons in C-H bonds are ...energy than those in C-O or H-O bonds
high energy electrons higher
170
descibe respiration quick
During glycolysis, each glucose molecule is broken down into two molecules of the compound pyruvate. In eukaryotic cells, as shown here, the pyruvate enters the mitochondrion. There it is oxidized to acetyl CoA, which is further oxidized to CO2 in the citric acid cycle. NADH and a similar electron carrier, a coenzyme called FADH2, transfer electrons derived from glucose to electron transport chains, which are built into the inner mitochondrial membrane. (In prokaryotes, the electron transport chains are located in the plasma membrane.) During oxidative phosphorylation, electron transport chains convert the chemical energy to a form used for ATP synthesis in the process called chemiosmosis​ ​
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how do electron carriers link orgnaic molecule oxidation to the ETC
NAD+ is an electron carrier​ Accepts high energy electrons from organic molecules​ Donate them to the electron transport chain​ Cannot be transported into/out of the mitochondria directly so must be regenerated​
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descibe NAD+
nicotinamide adenine dinucleotide, describes its structure—the molecule consists of two nucleotides joined together at their phosphate groups (shown in yellow). (Nicotinamide is a nitrogenous base, although not one that is present in DNA or RNA; see Figure 5.24.) The enzymatic transfer of 2 electrons and 1 proton (H+ ) from an organic molecule in food to NAD+ reduces the NAD+ to NADH: Most of the electrons removed from food are transferred initially to NAD+ , forming NADH​
173
explain how hydrogen and oxygen react in repiration
In cellular respiration, the same reaction occurs in stages: An electron transport chain breaks the “fall” of electrons in this reaction into a series of smaller steps and stores some of the released energy in a form that can be used to make ATP. (The rest of the energy is released as heat.)​
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where does glycolysis take place and how much energy is released
the cytosol small amout of energy
175
What type of phosphorylation occurs in glycolysis
substrate level phosphorylation
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where does the pyruvatre go
enters the mitrochondria
177
where does the krebs cycle take place
matrix of mitrochondria
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where is the ETC located
inner membrane of the mitrochondria
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detailed glycoloysis explation yielfing ATP
Hexokinase transfers a phosphate group from ATP to glucose, making it more chemically reactive. The charge on the phosphate also traps the sugar in the cell. Glucose 6- phosphate is converted to fructose 6-phosphate. Phosphofructokinase transfers a phosphate group from ATP to the opposite end of the sugar, investing a second molecule of ATP. This is a key step for regulation of glycolysis. Aldolase cleaves the sugar molecule into two different three-carbon sugars. Conversion between DHAP and G3P: This reaction never reaches equilibrium; G3P is used in the next step as fast as it forms. Two sequential reactions: (1) The sugar is oxidized by the transfer of electrons to NAD+, forming NADH. (2) Using energy from this exergonic redox reaction, a phosphate group is attached to the oxidized substrate, making a high-energy product. The phosphate group is transferred to ADP (substrate-level phosphorylation) in an exergonic reaction. The carbonyl group of G3P has been oxidized to the carboxyl group (—COO–) of an organic acid (3-phosphoglycerate). This enzyme relocates the remaining phosphate group. Enolase causes a double bond to form in the substrate by extracting a water molecule, yielding phosphoenolpyruvate (PEP), a compound with a very high potential energy. The phosphate group is transferred from PEP to ADP (a second example of substrate-level phosphorylation), forming pyruvate.​
180
how is pyruvate transported into the mitrochondiral matrix
pyruvate is charged to must enter mitrochondripn via active transport , with the help of a transport protein
181
what type of phosphorylation does the krebs cycle use
substrate level
182
does FAD or NAD+ accept electrons of a lower energy
FAD
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how specificalt are carbons cycled through the citric acid cycle
Notice that the carbon atoms that enter the cycle from acetyl CoA do not leave the cycle in the same turn. They remain in the cycle, occupying a different location in the molecules on their next turn, after another acetyl group is added. Therefore, the oxaloacetate regenerated at step 8 is made up of different carbon atoms each time around. In eukaryotic cells
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how does the ETC release energy
This generates energy via redox reactions, which occurs when there is a transfer of one or more electrons from one reactant to another. The reactant which loses an electron is oxidized while the reactant receiving the electron is reduced. This process is associated with the release of energy.​
185
what does the ETC consist of
collection of multiprotein complexes embedded u the inner membrane of the mitrochondira Most components of the chain are proteins to which are attached prosthetic groups, these are non protein components essential for the catalytic functions
186
whats the first moleucle in the ETC called and why
flavoproteins its prosthetic group is flavin mononucleotide
187
descibe what occurs on the ETC
the first molecule is a flavoprotein, Electrons then pass onto an iron-sulphur protein and then to ubiquinone and then to a series of electron carriers termed cytochromes. The prosthetic groups of cytochromes have four organic rings surrounding an iron atom (like haemoglobin) except the iron of cytochromes transports electrons not oxygen.​ The last cytochrome in the chain passes its electrons onto oxygen, which picks up a pair of H+ to form water.​ FADH2 also transfers electrons into the electron transport chain but adds its electrons at a lower energy than that of NADH. FADH2 adds its electrons direct to ubiquinone.​ At the bottom of the chain is oxygen which is very electronegative. The overall energy drop from NADH to oxygen is 53kcal/mol, but this fall is broken up into a many small steps by the electron transport chain.​​
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descibe ATP sythase
ATP synthase is a large multiprotein complex which can be seen under the electron microscope in the inner membrane of the mitochondria and has a mushroom-like appearance.​
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descibe chemiosomosis
The ion gradient which drives ATP synthesis is a H+ gradient, which exists between the opposite sides of the inner membrane.​ It is the electron transport chain which generates and maintains this gradient. The electron transport chain uses the energy from the exergenic flow of electrons to pump H+ from the mitochondrial matrix into the intermembrane space.​ H+ then pass back thorough the ATP synthase and this exothermic process is used to attach inorganic phosphate to ADP, producing ATP. ​
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how does chemiosomsis couple to the ETC in atp sythesis
NADH and FADH2 shuttle high-energy electrons extracted from food during glycolysis and the citric acid cycle into an electron transport chain built into the inner mitochondrial membrane. The gold arrows trace the transport of electrons, which are finally passed to a terminal acceptor (O2, in the case of aerobic respiration) at the “downhill” end of the chain, forming water. Most of the electron carriers of the chain are grouped into four complexes (I–IV). Two mobile carriers, ubiquinone (Q) and cytochrome c (Cyt c), move rapidly, ferrying electrons between the large complexes. As the complexes shuttle electrons, they pump protons from the mitochondrial matrix into the intermembrane space. FADH2 deposits its electrons via complex II—at a lower energy level than complex I, where NADH deposits its electrons— and so results in fewer protons being pumped into the intermembrane space than occurs with NADH. Chemical energy that was originally harvested from food is transformed into a proton-motive force, a gradient of H+ across the membrane. 2 During chemiosmosis, the protons flow back down their gradient via ATP synthase, which is built into the membrane nearby. The ATP synthase harnesses the proton-motive force to phosphorylate ADP, forming ATP. Together, electron transport and chemiosmosis make up oxidative phosphorylation.​
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descibe ATP synthase
Fo portion is a H+ channel​ F1 head is site of ATP synthesis​ Movement of H+ through Fo:​ causes rotation of the rotor and central stalk, while the stator keeps the enzymatic F1 stationary​ forces sequential conformational changes in the central stalk and F1​ provides the energy for ATP synthesis ​ 10H+ moving back into matrix generates ~3 ATP molecules​ ​ ​
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give an example of a mitrchondrial poison
cyanide prevents the passage of electrons from one of the cytochromes thereby blocking the ETC DNP, makes the inner membrane leaky to H+ so that the gradient cannot be established, ETC still works but energy is released as heat
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descibe brown fat
specialized type of adipose tissue Function of the mitochondria in brown fat is to produce heat​ Found in large amounts in newborn babies​
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what is thermogenin
Thermogenin is a H+ channel in inner membrane in brown fat mitochondria​ H+ leak back without passing through ATP synthase  no ATP produced​ Energy produced by the electron transport chain is released as heat​ ​
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what is MERRF(Myoclonic epilepsy and ragged-red fiber disease)
Mitochondrial genetic disease​ Mutation in the mitochondrially encoded tRNA Lys gene​ Affects the translation of mitochondrially encoded proteins​ assembly of the electron transport chain complexes disrupted​ reduced mitochondrial respiratory function​ Abnormal mitochondrial morphology​ Multisystem disease primarily affecting muscles and nerves  epilepsy and general muscle weakness​ No cure​
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what are mitrochondira inherted from
only the mother
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what has been developsed to avoid pssing on defecive mitrchondrial
new IVF technique - the embryo hs 3 genetic parents
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what are photoautptrophs
organisms that can make theirown energy using ligth and co2 via the process or photosythesis
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desiceb the structure of a cholorplast
Chloroplasts are surrounded by an outer and an inner membrane which together are termed the envelope.​ ​ The envelope encloses an aqueous compartment called the stroma in which starch granules are usually found.​ ​ The inner most compartment is the thylakoid space which is enclosed by the thylakoid membrane. In some chloroplasts the thylakoid membrane is formed into dense stacks called grana. Chlorophyll is present in the thylakoid membrane. The thylakoid is responsible for the steps of photosynthesis which convert light energy into chemical energy.​ ​
200
where does the calvin cycle take place
stroma
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where does the ligth dependent reaction take place
thylakoid membrane
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what does the light dependent reaction do
uses solar energy to make atp and nadph which suplys chemical energy and reducing power to the calvin cycle
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describe the light dependent reaction
. At least three steps in the light reactions contribute to the H+ gradient by increasing H+ concentration in the thylakoid space: 1 Water is split by photosystem II on the side of the membrane facing the thylakoid space; 2 as plastoquinone (Pq) transfers electrons to the cytochrome complex, four protons are translocated across the membrane into the thylakoid space; and 3 a hydrogen ion is removed from the stroma when it is taken up by NADP+ . Notice that in step 2, hydrogen ions are being pumped from the stroma into the thylakoid space, The diffusion of H+ from the thylakoid space back to the stroma (along the H+ concentration gradient) powers the ATP synthase. These light-driven reactions store chemical energy in NADPH and ATP, which shuttle the energy to the carbohydrate-producing Calvin cycle.​
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explain the ligth reaction simple steps
​ The light reaction converts solar energy to chemical energy​ ​ Light energy absorbed by chlorophyll in the thylakoid membranes is used to transfer electrons and hydrogen to the electron carrier NADP+ so that it becomes NADPH. ​ ​ Water is split during this process and oxygen given off as a by product.​ ​ ATP is also generated from ADP and inorganic phosphate​ ​ The thylakoid membranes of the chloroplast are the site of the light reactions
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how is ligth energy absorbed in chlorophyll
When pigments absorb light energy as photons, an electron in the pigment is elevated to an orbital of higher energy.​ ​ There are several pigments in the thylakoid membranes: Chlorophyll a, Chlorophyll b and Carotenoids. Only Chlorophyll a can participate directly in the light reactions but the other pigments absorb light energy at different wavelengths and transfer this energy to Chlorophyll a. This broadens the range of wavelengths that can be used.​ ​ Generally when pigments absorb light, the electrons quickly drop down to their original energy losing their excess energy as heat. In the thylakoid membrane, a nearby molecule called a primary electron acceptor traps a high-energy electron that has absorbed the photon before it can drop back down.​ ​ Only one localised pair of Chlorophyll a molecules can actually donate their excited electrons to the primary electron acceptor. This is called the reaction centre. The other pigment molecules function as light-gathering antennae which collect energy from the photons and pass it inwards to the reaction centre. The reaction centre and the primary electron acceptor together are termed a Photosystem. ​
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how does a spectrophotometer wrork
spectrophotometer measures the relative amounts of light of different wavelengths absorbed and transmitted by a pigment solution. 1 White light is separated into colors (wavelengths) by a prism. 2 One by one, the different colors of light are passed through the sample (chlorophyll in this example). Green light and blue light are shown here. 3 The transmitted light strikes a photoelectric tube, which converts the light energy to electricity. 4 The electric current is measured by a galvanometer. The meter indicates the fraction of light transmitted through the sample, from which we can determine the amount of light absorbed.​
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descibe the classic experiment that reveled which wavelengths of light are photosythetically important
Exposed algae filament to different wavelengths of light.​ Placed aerobic bacteria with the algae. ​ Higher concentration of oxygen allowed the aerobic bacteria to proliferate more.​ Accumulated near the parts of the algae illuminated with red and blue light = the wavelengths that work most efficiently for photosynthesis. ​
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how do chlorophyll a and b differ
only in one functional group bonded to the porphyrin ring
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role of antennae pigments in photosystems
Photosystems have antennae pigment molecules which absorb photons​ Energy transferred between pigments to the central pair chlorophyll​ Electrons elevated to higher energy state and taken by primary electron acceptor​
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what are the 2 photosytemrs in the ligth reaction
Photosystem I absorbs light energy best at 700nm so the reaction centre is called P700.​ ​ Photosystem II absorbs light energy best at 680nm so the reaction centre is called P680.​ ​
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photosytems 1 and 2 worktogther to do what
produce a non cyclcic electron flow to genertae nadph and atp and to spllit water
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descibe the non cylci electron flow
Light excites electrons from P700 which pass to the electron acceptor, but are then passed to NADP+ to produce NADPH.​ ​ So P700 is now in a very oxidised state​ ​ In photosystem II, P680 also becomes excited and donates an electron to its primary acceptor. This electron then passes down an electron transport chain until it is eventually accepted by the oxidised P700. The energy generated by this process is used pump hydrogen ions out of thylakoid membrane and generate a hydrogen gradient which is used to ATP synthase to produce ATP .​ ​ The P680 is now in an oxidised state and P680 gets its electrons from a water molecule, thus splitting it, and generating oxygen.​ ​
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descibr cyclic electron flow only using PS1
​ Photosystem I can operate alone to produce ATP. This is termed cyclic electron flow. Electrons are passed from the primary electron acceptor through a chain which includes ferredoxin, the cytochromes and a copper containing protein called plastocyanin. The electron is eventually passed back to P700.​ ​ At each step the electron lose energy and this energy is used to pump hydrogen ions across the thylakoid membrane.​ ​ This generates a hydrogen gradient across the membrane which is used to drive an ATP synthase molecule which generates ATP (just like in mitochondria).​ ​ Cyclic electron flow uses a single photosystem to make ATP and does not produce NADPH or oxyge
214
descibe the calvin cycle
carbon enters n the from of co2 and leaves in the from of sugar requires ATP as an energy soryce abd consumes NADPH as a source of higher enegry electrons Generates hexose phosphates for starch (storage), cellulose (cell walls) and sucrose (translocation), lipids (cell membranes) and amino acids (protein synthesis).​
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similarities between chloroplasta and mitrochondrias chemiososmosis
both chloroplasts and mitochondria use the same basic mechanism to generate ATP.​ ​ In both cases, an electron transport chain located in a membrane pumps hydrogen ions across the membrane. The energy for this process is generated by passing electron through a series of progressively more electro-negative carriers.​ ​ The membrane also contains an ATP synthase complex which uses gradient of hydrogen ions for the phosphorylation of ADP to ATP.​ both have a similar endosymbiotic origin​ Some of the electron carriers including the quinones and cytochromes are very similar in mitochondria and chloroplasts.​ ​
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what are the differecnes bteween mitochondira and chloroplasts processes
In mitochondria, the electron transport chain pumps hydrogen ions out of the matrix. In chloroplasts, the electron transport chain pumps into the thylakoid compartment.​ ​ In mitochondria, the high energy electrons fed into the electron transport chain come from the oxidation of food molecules. In chloroplasts, the high energy electrons are generated in the photosystems by the absorption of photons. ​
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what is the cytoskeleton
3D system of fibers running through the cytosol. disscovered with electron microscopy. its important in cell mobility , cell division, cell shape and movement of organelles in chromasomes
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what are the 3 main types of fibers in the cytoskeletom
microfilaments microtubules intermediate filaments
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descibe the microfilaments
About 7-8 nm in diameter and are composed of two actin chains twisted around each other. They have a variety of structural and locomotor functions​
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descibe microtubules
Straight hollow rods 25nm in diameter and up to 20 microns long, and are constructed from globular proteins called Tubulins​
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descibe intermediate filaments
8-12nm in diameter and are made up of a diverse group of proteins. Tend to be permanent fixtures, and are important in maintaining the shape of the cell, as well as maintaining the position of certain organelles​
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what is the main function of microfilaments
maintenece of cell shape changes in cell shape muscle contractions cytoplasmi streaming cell mobility ( pseudopodia) cell division (cleavage furrow formation)
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what 2 types of actin is microfilaments made of
G actin F actin
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whatt holds together the two lobes of the actin monomer
ATP
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describe the assembly of g and f actin in microfilaments
g actin assembles into long, helical f actin polymers
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what movements are diven by actin polymerization
white blood cell transmigration cellular extensions- eg. the acrosome reaction in echinoderm sperm
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t or f microfilaments are present in all eukaryotic cells
t
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describe microfilaments
Most animal cells have a network of actin filaments just below the cell surface termed the Cell Cortex; this cortex supports the plasma membrane and facilitates cell movement.​ ​ Composed of actin which is a globular protein (termed G actin, molecular weight 42,000 kilodaltons)​ ​ Soluble actin monomers polymerize to form insoluble filamentous actin (F actin), a double right-handed helical molecule.​
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functions of microfilaments
Muscle contraction where they interact with myosin filaments.​ Cell movement and migration​ Cell separation during cytokinesis​ Cell shape​ Structural roles – formation of microvilli
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desicbe myosin- actin motor proteins
myosin use energy from atp hydrolysis to walk along actin filaments.c omtraction or transportation roles
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what does phalloidin do
toxins such as phallodini bind to f actin preventing disassemble- attached to a flourescent tag can be used to stain actin q
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structure of microtubules
hollow tubes, wall consists of 13 column sof tublin mlecules
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diameter of microtubules
25nm with 15 nm lumen
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what protein subunits are microtubules made of
tubulin, a dimer consisting of alpha- tubulin and beta tubulin
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what are the main functions of microtubules
maintenance of cell shape cell mobility ( as in cilia or flagella ) chromasome movements in cell division organelle movement
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what is GTP binded to in microtubulin
alpha tubulin
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what is GDP binded to in microtubules
beta- tubulin
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what is taxol binded to in microtubules
beta-tubules
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what is the medical importance of microtubule binding drugs
Microtubule/tubulin-binding drugs are used to treat a variety​ of diseases, including cancer. ​ ​ For example the cancer drug taxol used for ovarian cancer, ​ breast cancer and lung cancer which prevents microtubule ​ disassembly and therefore cell division in cancer cells.​ ​
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structure of microtubule
consist of a core of axonemal microtubules ensheathed in an extension of the plasma membrane 9 doublets of microtubules are arranged in a ring an dconnected to 2 central icrotubules by radial spokes- 9+2 qrrangement
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describe dynein in cilia and flagella
Each doublet is connected to its neighbour by sidearms composed of Dynein, which contracts at the expense of ATP forcing the doublets to move relative to each other.​ Crosslinks prevent the doublets sliding past each other, so that the flagella or cilia bend.
241
look into nexin crosslinking = how dynein walking oves flagella and cilia
242
what does nexin crosslinking cause
in isolated cili, without nexin crosslimks movement of dynein motor proteins causes microtubule doubles to dlife past one another when nexin is present to cross link the doublets. they cannot slide and the force gernated by dyein movement cuases the cilium to blend
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what is a differance between cilia and flagella
Cilia are shorter (2-20µm) and more numerous than flagella (10-200µm), but both have the same structure. ​
244
descibe prokarotic flagella
made of protein subunits protrudes through cell wall and cell membrane stiff , twirl like a propella
245
structure of eukaryotic flagellum
a bundle (9+2) of microtubules covered by cell membrane whippy action
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what do kinesin and dynein motor proteins do
transport membrane bound vesicles, proteins and organelles along microtubules at the expense of ATP kinesis move cargo towards the + end of the micrptubules ( anterograde) whilst most dyneins transport cargo towards the 0 end of the microtubules ( retrograde )
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what are the 2 main types of microtubules
cytoplasmic - more dynamic and loosely organized found in the cytoplasm.​ axonemal - highly organized and stable found in cilia flagella and basal bodies​ ​
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how are microtubules formed
from the polymerization of tubulin dimers
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what are cytoplasmic microtubuars involved in
maintenanceof cell shape, cell movement , transport of vesicles within the cell and the separateion of chromosomes during cell division
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how do microtubules act at "tracks "
tracks on which the vesicles and small particles can move . this occurs via kinesin dynein. these are motor proteins one end binds to a microtubule while the other end of attached to a vesicle
251
what is the structure of intermediate filaments
fibourous proteins supercoiled into thicker cables
252
diameter of intermediate filaments
8-10 nm
253
what are the protein subuntis of intermediatw filaments
one of severale different proteins such as keratin, depedning on cell type
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what are the main functions of intemediate filaments
maintenance of cell shape, tneison bearing elements anchorage of nucleus and certain other organelles formation of nucelar lamina cell junctions
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types of intermediate filaments on slide 37 of lec 7
256
what is epidermolysis bullosa simplex due to
a defect in the keratin 14 gene
257
what is the width of cells called
basal
258
what is the top length of cells called
apical
259
what is the bottom legth of cells called
lateral
260
name the 3 types of cell junctions
impermeable junctions adhesive junctions communicating junctions
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what is an impermeable junction
prevents the passage of molecules between cells. tight junctions
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what are adhesive junctions
these emchanically hold cells togther. adherens junctions and adhesive desmosomes
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what are communicating junctions
passage of small molecules between cells. gap junctions ro chemical synapses
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what is the fence function of impermeable junctions
: Separate the apical plasma membrane from the basal plasma membrane, thus allowing them to have different compositions. This also gives rise to cellular polarity. ​
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what is the barrier/gate function of impermeable junctions
prevent molecules from leaking between adjacent cells
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what do the tight junctions do in the parietal cells in the stomach
The apical surface contains proton and chloride ion pumps which generate HCl​ ​ Tight junctions keep the apical membrane components separate from the basal membrane components.​ ​ In the gut, this stops acid being pumped into the blood stream.​
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what are the 4 anchoring junctions
adherens junctions desmosomes focal adhesions 'hemi-desmosomes
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what are the two types of tight junction proteins
transmembrane and cytosolic
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what do transmembrane tight junction proteins span
span the plasma membrane form actual physical barrier
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function of transmembran eprotein
connect each cell to each cell physicalt regulates permeability
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what are transmembrane proteins anchored by
cytosolic proteins
272
what are cytosolic proteins inforved in
signalling polarity
273
what are cytosolic proteins connected to the cytoskeleton by
microfilaments
274
what are the 4 types of anchoring junctions
adherens, desmosmes, focal adhesions, hemidesmosomes
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where do adheren junctions lie
directly below the tight junctionsf
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functions of anchoring junctions
resist streach and abresion, keep the cell together, keep the barrier intact, extremely strong
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give a real life example of the function of adherens junctions
cells need to accommodate streaching stomach cells when eatchung lungs in inhalation bladder when filling with urine vasodilation
278
what are adherens junctions made up of
cadherins, connect cells to microfilamant actin
279
what are adherens involved in -
intracellular signalling regulation
280
what do adherence proteins have as part of their complex
transmembrane and cytosolic proteins
281
wha tis the major transmembrane protein in adherence junctions
E- cadherins ( E is epithelium )
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where are cadherins found
within the paracellular spcae, this is the transmembrane proteins that crosses the plasma membrane,
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what do E cadherins bind to
bind each cellular E cadherin to another E cadherin, they form a phsycial barrier brtweenn cells
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what molecule are E cadherins depended on, what would happne if iy wasnt present
calcium they are calcium dependent proteins if calcium is not present the e-cadherins cant bind to another e cadherin
285
what are ecadherins bound to
beta-catenin
286
what are beta catenins
cytosolic protein'
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beta catenins and e-cadherens form what comlex
cadherins-catenin complex `
288
what is the job of beta catenin
anchor the adherence junction to the cytoskeleton via actin or micro filaments
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function of beta caratin in signal transducton and explain what happens
regulation of wnt signalling during embryonic developement. if certain e-cadherins link break between cells such as if there isnt any calcium. this triggers the depolarisation or dedifferentiation of cells. you then loose the apical basal composition of cells - the cell is depolarised. the beta catenin will translocate into the nucelu,this then leads to cell tissue morphogenesis and fibrosis and the development of epithelium-mesenchyl transition. this change allows the cell to migrate. Eg. Duting a wound ​
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when else does cell tissue morphogenesis and fibrosis happen
cancer- altering protein structures such as e-cadherins. prevents cells binding togther. causes cells to clump togther and migrate away
291
what is the most strong anchoring junction
desmosomes
292
what do desmosomes do
link cells together , they interlock with extracellular spcae with adjacent cells involved in stuctural integrity and can withstand mechnaical stress
293
what are desmosomes dependent on
calcium
294
what are desmosomes depeendnt on
cadheins - desmoglein, desmocolin
295
what effect does desmosomes being strong have on tissues
so strong they can spread the force recived by any sort of signal across the whole tissue
296
how are desmosomes are connected to cytoskeleton by hwat
intermediate filaments
297
what do focal adhesions and hemidesmomoes have in comon
they don't connect cells to cells they connect to the substrate or extracellular matric to the cytoskeleton.
298
how do focal adhesions connect to subtstrate or extracellular matrix
microfilament
299
how do hemidesmosomes connect to substrate or extrcellular matirx
intermediate filament
300
what are both focal adhesions and hemidesmosomes made up of
intergrins
301
hemidesmosomes connect the cell to the .......
basal lamina
302
what is the most common type of cell junction
gap junctions
303
where are gap junctions present
all animals
304
what are gap junctinos
tiny pores composed of proteins called connexins. 6 connexins on each cell from a gap junction.
305
6 connexins = 1
conexon
306
what do gap junctions do
share ions, signalling molecules, can pass eletrical siganls . can also signal if there is a problem - called paraci=rine signalling - this is important during infections and leads to programmed cell death
307
what does permeability of a gap junction depend on
intercellular PH and intracellular calcium levels
308
what do connexins form
cylindrical channels
309
signficamce of gap junctions in heart beat
propagation of the precisley orchestrated pattern of current flow that givern the regular rythm of the health heart
310
cellular functions of connexins
1- mediate electrical communicatino to effect contraction and motility 2- allow passage of molecules and ions between cells 3- modulate cell polarity and directional migration
311
what dissorders can connexins issues cause
inflamoratory bowel disease gastrointestinal infection autism spectrum disorder
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why do cells need to divide
1- new organisims 2- growth 3- cell replacemnt ( wear and tear, programmed cell death )
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what are the basic requirements for a cell to divide effectively
1- the DNA of the parent cell must be duplicated 2- the chromosmes conatining the replicated dna must then be physically segregated into the two daughter cells 3- the daugter cells must physically divide from each other
314
what is binary fission
Relatively simple process by which bacteria duplicate their DNA and segregate their chromosome into two daughter cells
315
explain the process of binary fission
1- chromosomes replication beings. them one copy of the origin moves rapidly towards the other end of the cell 2- replication continues. one copy of the origion is now at each end of the cell 3- replication finishes. the plasma membrane grows inwards and a new cell wall is deposited, two daughter cell result
316
what are the phases in interphase of the cell cycle. and what are the main points of each phase
G1= gap cell grows prepares to replicate DNA S= sythesis cell grows synthesis of duplicate DNA ready for mitosis G2 = gap cell grows prepares for mitosis
317
define mitosis
the physical process of segregating chromosomes inot daugher cells
318
qhat do chromosomes consist of at the start of mitosis
the chromoeomes constist of two sister chromatids linked at the centromere
319
describe G2 of interphase
intact nuclar envelope chromosomes replicated - remain indistinct as loosley packed chromatin ( DNA and protein ) fibres centrosome replicated microtubules extend radically forming asters
320
describe prophase
chromatin fibers condense forming discrete chromosomes nuceoli disappear centrosomes moves away from each other mitotic spindle begins to form
321
descibe prometaphase
breakdown of nuclear envelope some microtubules attach to chromosomes at they kinetochores other microtubules interact with those from opposite poles
322
describe metaphase
centrosomes at opposite poles chromosmes align on the metaphase plate sister kinetchores attached to microtubules coming from opposotes poles
323
descibe anaphase
begins with separation of centrosomes sister chromatids move towards opposite poles of the cell each chromatid becomes a new chromasomes poles move futher apart
324
descibe telophase
elongation of cell by polar microtubules daugter nucleoli begin to form at poles of cell nucelar envelopes from chromatin beind to condence
325
what is the functions of mitotic spindles
to organise chromatids along the metaphase plate and then to pull sister chromatids apart
326
name the 3 microtubules motors
astral motors kinetochore motors mom-kinetochroe/ polar motors
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descibe astral motors ( dynein )
pull astral microtubules towards poles during prophase microtubules de polymerise and shorten hold astral microtubules in place during metaphase and later
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descibe kinetochore motors
attach chromsomes to microtubules pull on microtubules during anaphase - chromsomes move towards centrosomes microtubules de polymerise and get shorten
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descibe non-kinetochore / polar motors
motors are attached to a microtubule from either side where the polar microtubules overlap motors push the microtubules away in opposite directions during metaphase and anaphase microtubules polymerise and get longer cell elongates
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what do motor proteins do
separate sister chromatids during anaphase
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in anaphase A shortining of ....... microtubules; movement of daughter chromosomes to poles; force generated mainley at....
kintochore kintochores
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in anaphase B 1) a sliding force is generated between ....... microtubules from opposite polares to push the polaes apart ; the ........ microtubules also elongate 2) a pulling force acts dircetly on.....
interpolar interpolar the polaes to move them apart
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desicbe how chromsomal separation is achieved by a combination of pushing and pulling
pulling ( dynein) - kintochore motors pull chromosomes towards the centrosome/ pole - astral motors pull centrosomes towards inner face of the plasma membrane - both shorten depolymerise microtubules pushing ( kinesin ) - non-kinetochores / polar motors add subunits ( polymerises ) microtubules to druve the poles of the spindle apart. this elongates the cell to aid telophase / cytokensis
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explain how the physical separation of chromomes pairs by the mitotic spindle occurs in anaphase
1. Proteins holding sister chromatids together are inactivated 2. Chromatids separate 3. Kinetochore microtubules have motor proteins (dynein) which ‘walk’ a chromosome to the nearest pole 4. Microtubules shorten by depolymerisation at their kinetochore ends 5-Non-kinetochore microtubules elongate whole cell during anaphase Motor proteins (kinesin) attach to microtubules and lengthen them by addition of subunits
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descibe cytokinesis in animal cells
microfilaments form a ring at the furrow ring contracts- owing to interaction between actin and mysoin filaments furrow deepens until cell is piched in two
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descibe cytokinesis in plant cells
cell plates froms at equoritoral plane of cell cell wall froms - from plate contents
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why is correct regulation of cell division important
1) development: organs and body parts need to be correct size/ shape 2) injury: cells need to divide followinf injury but stoop when damage is prepared 3) adaptive responses:
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give 2 examples for adaptive responses in cell division
cells in bone marrow resond to low O2- produce more red blood cells - need to stop when O2 return to normal lymphocytes- division triggered in response to antigen - needs to be cotorlled
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what 2 signals control where and when cells divide
external and internal signal s
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desicbe external signals
diffusable chemical signals produces by other cells which tell the cell in question how to behave wg. growth factors ( mitogens )
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desicbe inernal signals
chemical signals produced internally by the cell itself in order to regulate its own division - pesent in the cytoplasm of cells eg. cyclin dependent kinases
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t or f external signals only promtoe cell division
f they can also inhibit ot
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what are external signlas known as
mitogens or anti-mitogens
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what happens in the absesnce of mitogens
s phase cyclins ( i.e those cyclins which drive the cell inot S phase ) are not made
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without sustained mitogen stimulation cells will not progress through ....
G1 checkpoint
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what do cells enter instead. if they dont pass through G1 checkpoint
G0 - quite phase or quiescence
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what do mitogens bind to
receptors in plasma membrane and promote cell growth
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what does PDGF stand for and what is it an example of
platelet derived growth factors an axample of an external growth factor
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where are PDGF released from
platelets in response to injury
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what do pdgf bind to
receptors on surface of skin cells and causes them to strat dividing
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how were internal siganls frist indentified
by fusing cells from different stanges of the cell cycle
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describe the cell fusion expermient + the conclusions
M phase + G2 = M phase conclsion : there is a mitosis promtoing factor in M phase cells M phase + G1 or G2 or S = M phase conclusion: cells at any stage of the cell cycle can be stimulted by M phase cells to enter mitsosis - resonse is not unique to G2 cells S + G2 = S conclusion : there is an s phase promoting factor in s phase cells S + G2 = conclusion: although there is an S phase promoting factor in s phase cells, only G1 cells respond t othis factpr
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why does the cell need internal signals to control division
uncontrolled cell division is a hall mark of cancer checkpoints enable cells to stop dividing if the correct signals are not present checkpoints allow cells to review current circumstances and prevent untimely exit from each cell cycle phase if cell proceeds from one phase of the cycle to the next inappropriately, this can cause genetic instability genetic instability can cause cancer
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what are the tree major checkpoints of the cell cycle
G1 G2 metaphase or SAC
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what does the G1 checkpoint do
commits cell to dna replication and cell division it check if the cell is a suitible size, has it recicved the appropriate external signals
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what does the G2 checkpoint do
cells make a decision whether or not to enter mitosis is the cell a suitbale size, is dna replicated , is environemnt favourable
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how where cyclins discovered and by who
sir tim hunt in 1982 Observed that, following fertilisation, cells in sea urchin early embryos divided SYNCHRONOUSLY ​ ​ Whole population of cells at same stage of cell cycle as opposed to a mixed population at different stages​ ​ Found a group of proteins levels of which increased and decreased (cycled) between INTERPHASE and MITOTIC PHASE - CYCLINSv
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what are the internal molecular signals regulating G1 and G2 checkpoitns
cyclin-dependent kinases cyclins
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when does degration of cyclins occur
at the end of interphase / start of mitosis
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what is the combintion of cdk and cyclin called
promoting factor
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what do promoting factors do
contol progression of the cell inot the next phase of the cell cyle
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slide 21
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