protein structure and function Flashcards

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1
Q

How do we get our essential amino acids?

A

they come from food in our diet

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2
Q

How do we get our non-essential amino acids?

A

they are made by the body from the essential amino acids or from the breakdown of proteins

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3
Q

How are peptide bonds formed?

A
  • generated by peptidyl transferase
  • condensation to form covalent bond
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4
Q

Describe how alpha helixes look

A
  • spiral
  • side chains face outwards
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5
Q

How are alpha helixes formed?

A
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6
Q

Describe how beta pleated sheets look

A
  • flat structure
  • side chains extended above and below beta sheet
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7
Q

How are beta sheets formed?

A

hydrogen bonds form between carbonyl groups and an amino acid of neighbouring chain

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8
Q

What are two other possible secondary structures?

A
  • loops and turns
  • random coils
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9
Q

What is a coiled coil?

A
  • 2 or 3 alpha-helixes wind around each other forming a coiled coil
  • e.g keratin or collagen
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10
Q

Is the folding process energetically favorable or not ?

A

it is energetically favourable

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10
Q

Finish this sentence: Proteins spontaneously fold into a 3 dimensional….

A

conformation of the lowest free energy

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11
Q

What are molecular chaperones?

A

proteins that bind to the partially folded polypeptide chains and assist them in folding

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12
Q

How do chaperones help?

A
  • do not change 3D structure
  • speed up folding process
  • prevent protein aggregation
  • reduct non-productive intermediates
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13
Q

What are the two types of molecular chaperones ?

A
  • heat shock proteins
  • chaperonins
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14
Q

What are post translational modifications?

A

processing events resulting from proteolytic cleavage or the covalent addition of a modifying group

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15
Q

What is phosphorylation?

A

addition of a phosphate to specific amino acids regulating the activity of the protein

16
Q

What is glycosylation?

A

addition of carbohydrates to specific sites on the protein

17
Q

What is ubiquitination?

A

addition of ubiquitin can target the protein for destruction by the proteasome

18
Q

What are the symptoms of cystic fibrosis due to?

A
  • 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
19
Q

What does CTFR stand for (in cystic fibrosis)?

A

Cystic Fibrosis Transmembrane conductance Regulator

20
Q

What is Alzheimer’s Disease characterised by?

A

progressive memory loss and cognitive decline

21
Q

What is alzheimer’s caused by

A
  • misfolding of amyloid beta (form tightly packed beta sheets)
  • causing amyloid beta plaques and tau
  • causes intracellular neurofibrillary tangles
22
Q

What determines how the protein folds?

A

the distribution of hydrophobic and hydrophilic side chains along the backbone

23
Q

What are the 3 types of post-translational modifications?

A
  • phosphorylation
  • glycosylation
  • ubiquitination