ECM-COLLAGEN Flashcards

1
Q

What does collagen comprise of

A

three alpha chains forming a triple helix

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2
Q

describe type 1 collagen

A

Type I collagen has chains from two different genes - its composition is [alpha1 (I)]2 ( alpha2(I)]. ( 2 alpha ones and one alpha 2 chain)

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3
Q

describe type ii and iii collagen

A

Types II and III collagen have only one chain type – their compositions are, therefore, [alpha 1 (II)]3 and [alpha 1 (III)]3

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4
Q

collagen characteristic is gl-x-y. What is typically x and y?

A

x=proline, y=hydroxyproline

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5
Q

Outline the biosynthesis of fibrillar collagen

A

1) synthesis of the pro alpha chain
2) hydroxylation of select prolines and lysine
3) Glycosylation of select hydroxylysines
4) self assembly of three pro alpha chains
5) pro collagen triple helix forms
6) secretion
7) cleavage of propeptides
8) self assembly into fibrils
9) aggregation of fibrils to form collagen fibre

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6
Q

Name the non-collagenous domains of newly synthesised collagen

A

N-terminal (left) and C terminal (right) propertides

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7
Q

What happens to the N-terminal and C terminal after secretion for fibrillar collagens

A

They remain attached

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8
Q

What happens to the N-terminal and C terminal after secretion for most collagens

A

They are removed

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9
Q

What 2 effects does cross linking have on collagen

A

provides tensile strength, provides stability

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10
Q

what 2 residues are involved in cross linking

A

lysine and hydroxylysine

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11
Q

Explain how vitamin C deficiency can cause scurvy (4 marks)

A

Prolyl and lysyl hydroxylases require Fe2+ and vitamin C

Contributes to interchain hydrogen bond formation.

Lysine and hydroxylysine are also modified in the formation of covalent crosslinkages. This takes place only after the collagen has been secreted.

Vitamin C-deficiency results in underhydroxylated collagens, with dramatic consequences for tissue stability (scurvy).

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12
Q

What is Ehlers-Danlos syndrome? (EDS)

A

are a group of inherited connective tissue disorders whose symptoms include stretchy skin and loose joints

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13
Q

Several disorders arise due to mutations in collagen, which negatively affect: (list 3)

A

.collagen production
.collagen structure
.collagen processing

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14
Q

what is type IV collagen

A

Network forming collagen present in all basement membrane

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15
Q

what are types IX and XII collagen

A

fibril-associated collagen which associate with fibrillar collagens regulating organisation of collagen fibres

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