what is the name for improper folding of a protein?
amyloidoses
which bonds are involved in the different levels of the protein structure?
primary-covalent peptide
secondary-hydrogen
tertiary-hydrogen,VDW, hydrophobic and philic,disulphide,ionic .
what are they key features of an alpha helix?
what are they key features of a beta pleated sheet?
- multiple interstrand h bonds
describe myoglobin
describe Hb
which state of Hb has a high affinity for oxygen and which has a low affinity?(Hbs affinity for O2 increases as more O2 binds)
Relaxed state=high affinity
tense state=low affinity
what effect does BPG have on HB affinity for o2 and why?
what effect does co2 and H+ have on o2 affinity?
- at sites of low ph and high h+ conc, and increased co2 (e.g. muscle tissue) more o2 released (Bohr)
what is secondary structure?
polypeptide chains that form alpha helices and beta sheets and bonding
what amino acid is substituted in sickle cell anaemia?
glutamate to valine
what are thalassaemias?
group of genetic disorders where there is an imbalance of alpha and beta subunits
which thalassaemias appear before and which appear after birth?
Beta=after birth
alpha=before birth
give an example of a non polar amino acid
glycine
give an example of an uncharged polar molecule
glutamine
give an example of a charged polar amino acid
histidine
What are motifs?
Folding pattern containing 1 or more elements of secondary structure (e.g. Beta,alpha,beta)
What type of inheritance is sickle cell anemia?
Autosomal recessive
What is amyloidoses?
Improper folding of protein- normally soluble protein becomes insoluble
What are the 2 properties of sickle cells?
- more rigid (block microvasculature)
Name 5 things that cause a sickle cell crisis.
What are the consequences of a sickle cell crisis?
Blockage of vessels causing infarction and thus necrosis (due to no blood supply,disease or injury and so cell death occurs)
How to combat sickle cell crisis