C2.1 Flashcards

Chemical Signalling (31 cards)

1
Q

Signalling Molecules

Ligand?

A
  • Molecules that bind reversibly to specific proteins
  • Re-usable signalling molecules released from one cell and recieved by another, initating a type of action potential in the target cell
  • E.g., hormones, nuerotransmitters.
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2
Q

Signalling Molecules

Receptors

A
  • A protein that has a compatible shape to a ligang and which initiates a response in a target cell.
  • They are only found in target cells for that particular ligand, enabling specific responses only in the necessary cells.
  • Most receptors are intergral proteins in cell membranes, yet some are intracelllular requiring ligands to enter the cell to initate a response.
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3
Q

Signalling Molecules

Signal Transduction Pathways?

A
  • A series of steps that start with activation of the receptor.
  • This causes the next step, which causes the next step and so on until the response in initiated.
  • Having several steps allows for more regulation and control of the response..
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4
Q

Signalling Molecules

Quorum Sensing?

A
  • The mechanism by which bactiera alter group behaviour depending on population density.
  • This allows for coordination of individual bacteria allowing them to act as a colony
    Done with signalling molecules released by bacteria
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5
Q

Signalling Molecules

Autoinducers?

A
  • The signalling molecule that cause quorum sensing
  • They are chemicals released by individual bacteria
  • If low bacteria density = concentration of autoinducers is low and the response is NOT inititated
  • If there’s many bacteria, the conc. of autoinducers is high and they signal responses in all inidividual bacteria –> group coordinated response.
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6
Q

Signalling Molecules

Bioluminescence by Quorum Sensing

A
  • Bioluminscne done by a colony of bacteria by qurorum sensing
  • Happens when reproducing individual bacteria release an autoinducer from their cell membranes
  • As the no. bacteria increase, the conc. of autoinducers increase –> reaches threshold level, pass into cells and bind to a lux receptor protien
  • This activates Lux, causing it to bind to a DNA site
  • This causes the transcription of the gene for Luminescent protein
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7
Q

Signalling Molecules

Chemical Type and Role of: HORMONES

A
  • Signalling chemicals secreted by specialized endocrine cells and carried through the circulatory system to act on target cells at distant body cells.
  • They are a very specific – can only bind with certain a specific recepter on its intended target cell.
  • They are chemically diverse (polar /non-polar)
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8
Q

Signalling Molecules

Chemical Type and Role of: Neurotransmitters

A
  • Signalling chemicals released from one cell that acts on neighbouring target cells
  • They don’t enter the bloodstream, they move through the synapse between two nuerons and bind to a receptor on the nearby nuerons.
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9
Q

Signalling Molecules

Chemical Type and Role of: Cytokines

Usually within the immune system

A
  • Glycoproteins that act as messengers between cells.
  • They can act locally on nearby cells & can enter the bloodstream to impact distant cells.
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10
Q

Signalling Molecules

Chemical Type and Role of: Calcium ions

A
  • A common ligand in animals
  • They act as a primary ligand in muscle contraction and hormone secretion
  • In muscle fibres, Ca is pumped into the sacroplasmic reticulum (form of ER)
  • When muscle fibre recieves this electrical signal, Ca ions diffuse out and bind to proteins (actin!) allowing for muscle conctraction.
  • In nuerons, Ca triggers the release of nuerotransmitters
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11
Q

Signalling Molecules

Benefit of a Chemically Diverse Range of Ligands

A
  • Key chemical differences include: size, polarity and make-up.
  • Distinct shapes allows for specialized action only on compatible receptors
  • Diverse structures enables some ligands to enter cells and others not, also ensures different types of cell signalling are possible.
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12
Q

Signalling Molecules

Transmembrane vs Intracellular Receptors

A
  • Intracellular receptors sit inside the cytoplasm of the cell/nucleus.
    1. Hydrophillic amino acids allowing them to remain dissolved in the cytoplasm.
    2. Ligands that bind to them are non-polar (must be able to cross plasma membrane to bind to them)
  • Transmembrane receptors are embedded in the membrane.
    1. Have a band of hydrophobic amino acids in contact with the phospholipids and polar amino acids on each side. (amphiprotic)
    2. Polar lignads that can’t cross the membrane bind to them.
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13
Q

Transmembrane Receptor, Transduction Pathways

Multi-pass protiens?

A
  • A transmembrane protien composed of many domains that thread back & forth across the membrane several times.
  • More complex intergral protins - ex: acetycholine receptor
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14
Q

Transmembrane Receptor, Transduction Pathways

G-protein?

A
  • A protien with a GDP attached to it
  • The G protein with GDP attached binds to a receptor (currently inactive)
  • IF GDP becomes GTP with the addition of a third phosphate, the G-protien becomes activated and leaves the receptor now with the energy to activate a nearby enzyme.
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15
Q

Transmembrane Receptor, Transduction Pathways

Secondary Messenger?

A
  • Helps in continuing the signal transduction pathway but isn’t the initial ligand.
  • The receptor (when activated), often initiates a secondary messenger that is intracellular and able to activate enzymes within the cystoplasm.
  • EX: Cyclic AMP
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16
Q

Transmembrane Receptor, Transduction Pathways

Cyclic AMP?

A
  • A secondary messenger in many signalling pathways - like in those using a G-protien.
  • The energy released from the activated G protin activates the membrane enzyme Adenyl cyclase - this activates cyclic AMP
  • Cyclic AMP binds to kinase enzymes in the cytoplasm, beginning a series of one enzymes activating (phophorylating) another until the response is initiated.
17
Q

Transmembrane Receptor, Transduction Pathways

Kinase?

A
  • An enzyme that catalyses the transfer of a phosphate group from ATP to another substance.
  • Kinase phosphorylates things – activates them, often leading to the production of ADP and a substate.
18
Q

Transmembrane Receptor, Transduction Pathways

Phosphorylated?

A
  • A phosphate is added to a substance.
  • ADP is phosphorylated to make ATP
  • Also used for when phosphate is removed from ATP and transferred to a protien ( often an enzyme ).
  • Often, the phosphorylated enzyme is now active & can carry out a reaction.
  • Phosphorylating a series of enzymes makes up signal transduction pathways
19
Q

Transmembrane Receptor, Transduction Pathways

Structure & Function of: Chemically Gated Ion Channels

A
  • Large, multi pass proteins with a central pore.
  • When ligand is not bound, the channel is closed (ions cant move through)
  • When ligand (usually nuerotransmitter) binds to the receptor, the ion channel opens and ions move through.
  • This influx of ions causes the cellular response, which is how nuerotransmitters lead action potentials - they bind to their receptor, initating an influx of sodium, causing the onset of action potentials.
20
Q

Transmembrane Receptor, Transduction Pathways

Structure & Function of: Enzymatic Receptors

A
  • Transmembrane receptors that are smaller, simpler in structure (single pass over multi pass).
  • Contain two key regions: an extracellular region that the ligand binds to and an intracellular region that is capable of enzymatic activity when the ligand binds to the extraceccular region.
  • Ex: Tyrosine Kinase Receptors
21
Q

Transmembrane Receptor, Transduction Pathways

Structure & Function of: G Protein coupled receptors

A
  • Another type of transmembrane protein, they are large multi pass proteins with a G-protien attached to the receptor (when inactive)
  • When ligand binds, the protien phosphorylates the G-protein, casuing it to detach and activate another separate enzyme.
  • EX: Epinephrine uses a G-protien coupled receptor
22
Q

Transmembrane Receptor, Transduction Pathways

Acetycholine Signalling Pathway

A
  • A neurotransmitter released from one nueron into a synapse
  • Then it binds to AChR (Acetylcholine receptor) leading to a shape change that opens the protein to create a hydrophillic channel, allowing for sodium ions to enter a channel into the cell, causing a depolarization inside the axon that initaties the action potential allowing the nuron to fire an electrical message.
23
Q

Transmembrane Receptor, Transduction Pathways

Epiniephrine Signalling Pathway

A
  • Epinephrine is a hormone released by the adrenal glands that travels by the bloodstream to target muslce cells & the liver.
  • It binds to a G-protien couple receptor
  • When it binds, the G-protien becomes activated and detaches, transfering energy to the enzyme adenyl cyclase, creating cAMP that activates the first in a series of phosphorylase kinases.
  • A possible end result: breakdown of glycogen into glucose
24
Q

Transmembrane Receptor, Transduction Pathways

Insulin Signalling Pathway

A
  • Insulin is a hormone that binds to an enzymatic transmembrane receptor (tyrosine kinase receptor)
  • Insulin binds to the extracellular domain of both ends of the receptor, pulling the two intracellular ends of the receptor close and the phosphate groups attached to it.
  • This enzyme is now active & transfer the phosphates to other protiens beginning the signal transduction pathway.
25
# Intracellular Receptor Signalling Pathways Receptor-Signal Complex?
* When steroid hormones enter cells they **bind to receptors** that are usually in the **cytoplasm**. * The hormone tends to **stay bound to the receptor** and they move into the nucleus **together**, often to act as a **transcription factor**. * This is called the **receptor-signal complex**
26
# Intracellular Receptor Signalling Pathways Chemical Characteristic to Cross a Membrane
* In order for a **ligand to bind to an intracellular receptor** it must pass through the membrane. * To do this, the ligand must be **hydrophobic/non polar** (lipid soluable) in order to **move through the fatty acid tails** of the bilayer. * Ligands are usually steriod hormones (sex hormones estrogen, progesterone and testerone.)
27
# Intracellular Receptor Signalling Pathways Steroid Hormone Impacts: Oestradiol | Involved in the menstrual cycle
* Released by the ovaries in response to gonadotropin hormones (FSH and LH), released by the anterior pituitary. * As ovaries release more estrogen, its **effect is to travel by the bloodstream to the hypothalamus**. * It **signals the hypothalamus** to **increase the release of GnRH** to the **pituitary** that increases the release of **FSH and LH** that stimulate the **maturation and eventual release of an egg**.
28
# Intracellular Receptor Signalling Pathways Steroid Hormone Impacts: Progesterone
* Function is to **thicken the lining of the uterus** to faciliate implantation. * Hence, one of the key target cells are that of the uterine wall. (target uterine cells) * Progesterone **enters these cells and lead to the response of thickening** (cell proliferation) and **vacularization** (increased blood vessels to the area
29
# Intracellular Receptor Signalling Pathways Chemically Diverse Ligands
* The only way that **intracellular receptors** can be accessed is by ligands that can cross the membrane. * This isn't possilbe with **large hormones** (insulin) or **small polar hormones** (ADH). * Such hormones nessecitate **transmembrane receptors**. * Small hormones made of steroid lipids can cross through **fatty acid tails** to access intracellular receptors. * Hence, having chemically unique ligands enables **distinctive intracellular receptor pathways to exist**
30
# Intracellular Receptor Signalling Pathways Negative Feedback Signalling Loops
* The release of ligands is carefully regulated, often by negative feedback loops. * The example: the regulation of the release of the hormones **insulin and glucagon** (which are ligands that bind to **transmembrane receptors**) * Ligand release is **halted when the body returns to a set point** so the signalling molecules are only binding to receptors when needed.
31
# Intracellular Receptor Signalling Pathways Fever as a Positive Feedback Loop | Non-hormonal example of a positive feedback loop
* Non-hormonal example of a positive feedback loop in response to **infection**. * The presence of a **pathogen** causes the release of specific cytokines, **pyrogens**, that increase the **body temperature**. * This increase **in body temp** reinforces the immune system **casuing the release of more pyrogens,** raising the fever **until the pathogens are disabled** from the **high temperature**.