protein structure and function Flashcards
How do we get our essential amino acids?
they come from food in our diet
How do we get our non-essential amino acids?
they are made by the body from the essential amino acids or from the breakdown of proteins
How are peptide bonds formed?
- generated by peptidyl transferase
- condensation to form covalent bond
Describe how alpha helixes look
- spiral
- side chains face outwards
How are alpha helixes formed?
Describe how beta pleated sheets look
- flat structure
- side chains extended above and below beta sheet
How are beta sheets formed?
hydrogen bonds form between carbonyl groups and an amino acid of neighbouring chain
What are two other possible secondary structures?
- loops and turns
- random coils
What is a coiled coil?
- 2 or 3 alpha-helixes wind around each other forming a coiled coil
- e.g keratin or collagen
Is the folding process energetically favorable or not ?
it is energetically favourable
Finish this sentence: Proteins spontaneously fold into a 3 dimensional….
conformation of the lowest free energy
What are molecular chaperones?
proteins that bind to the partially folded polypeptide chains and assist them in folding
How do chaperones help?
- do not change 3D structure
- speed up folding process
- prevent protein aggregation
- reduct non-productive intermediates
What are the two types of molecular chaperones ?
- heat shock proteins
- chaperonins
What are post translational modifications?
processing events resulting from proteolytic cleavage or the covalent addition of a modifying group
What is phosphorylation?
addition of a phosphate to specific amino acids regulating the activity of the protein
What is glycosylation?
addition of carbohydrates to specific sites on the protein
What is ubiquitination?
addition of ubiquitin can target the protein for destruction by the proteasome
What are the symptoms of cystic fibrosis due to?
- single deletion of amino acid phenylalanine at position 508
- mutant CTFR protein becomes stuck in endoplasmic reticulum leading to reduced chloride conductance out of cells
What does CTFR stand for (in cystic fibrosis)?
Cystic Fibrosis Transmembrane conductance Regulator
What is Alzheimer’s Disease characterised by?
progressive memory loss and cognitive decline
What is alzheimer’s caused by
- misfolding of amyloid beta (form tightly packed beta sheets)
- causing amyloid beta plaques and tau
- causes intracellular neurofibrillary tangles
What determines how the protein folds?
the distribution of hydrophobic and hydrophilic side chains along the backbone
What are the 3 types of post-translational modifications?
- phosphorylation
- glycosylation
- ubiquitination