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27 Cards in this Set

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  • Back
Where do antigens bind to antibodies?

What is this area made of?
N-terminus where the there are hypervariable loops (VL and VH)
What holds the chains together in an antibody?
disulfide bonds
what is a sequence on an antigen that the antibody recognizes called?
epitope
what kind of antibody recognizes only ONE epitope?
monoclonal antibodies only recognize one epitope on an antigen - they are more specific than polyclonal antibodies.
what are folds in immunoglobulin chains called?
immunoglobulin domains
what are 6 steps in intracellular maturation of collagen?
1. synthesis of pro-a-chain
2. hydroxylation of proline/lysine
3. glycosylation of hydroxylysines
4. self assembly of 3 pro-a-chains
5. procollagen 3 helix formation
6. secretion from secretory vesicle
which steps in intracellular maturation of collagen occur in the ER and Golgi compartments?
1. synth of pro-a-chains
2. hydroxylation
3. glycosylation
4. self-assembly of 3 pro-a-chains
are helices in tropocollagen alpha-helices?
no tropocollagen does not make alpha-helices
What is notable about primary structure of tropocollagen?
q 3rd residue is a GLYCINE

it is also PROLINE rich.
What is useful in having tropocollagen be "proline rich"?
N-C(alpha) bonds are locked - so this limits rotation and favors helical shape.
What stabilizes the primary structure of tropocollagen?
H-bonds
What rxn occurs when prolyl residue is hydroxylated?
prolyl residue + O2 + aKG (PROLYL-4-MONOOXYGENASE)---> 4-hydroxylprolyl + CO2 + Succinate
why does the hydroxylation rxn require aKG involvement?
the enzyme catalyzing this rxn is a monooxygenase - these require a second reducing agent, like aKG.
What cofactors are used to make the hydroxylation of proline and lysine go?
Fe and Vit C (Ascorbate)
What enzyme catalyzes the hydroxylation of lysine?
lysyl-5-monooxygenase

deficiency of this causes Ehlers-Danlos Syndrome IV
What rxn needs Vitamin C in the intracellular maturation of collagen?

What other cofactor does it need?

Deficiency in Vit C causes what dz?
The hydroxylation of prolyl residues.

Fe.

Scurvy - gum degeneration, skin lesions, blood v fragility, anemia
what is different about pro-alpha1 and pro-alpha2 from the rest of the tropocollagen structurally?

What step are we considering?
these "pro" collagen areas do NOT have glycine q3rd position and are NOT proline rich.

Formation of procollagen
What is the key step in formation of procollagen?

What step comes right before formation of procollagen?
Key step is the oxidation of cysteine into cystine. (***an important general mechanism for joining polypeptide chains).

Right after glycosylation. (Which occurs right after the hydroxylation of prolyl/lysine residues).
What happens after procollagen is made?
Procollagen is SOLUBLE and is secreted into extracellular space by fibroblasts. Then proteolytic enzymes snip off the pro-alpha1/2 chains. Then SELF-ASSEMBLY occurs.
What enzyme is responsible for the rxn which matures the collagen fiber?

What two conditions occur bc of deficiency of this?
lysyl oxidase

lathyrism = after eating sweet peas that degrade this enz

or Ehlers-Danlos Sydrome IX
Describe the lysyl oxidase rxn.
5-hydroxylysyl residue(LYSYL OXIDASE+H2O+O2)--->
5-hydroxyallysyl residue + H2O2 + NH4+
What is special about the product in the lysyl oxidase rxn? What is the product?
Product = 5-hydroxyallysyl residue

This residue has a new aldehyde group which is VERY reactive and makes RIGID cross-links bt collagen fibers.
What causes Type IX Ehler's Danlos syndrome?
low lysyl oxidase activity = NO MATURATION OF COLLAGEN FIBERS.
5-hydroxyallysl residue is not made.
What causes type VI Ehlers-Danlos syndrome?
deficiency in lysyl-5-monooxygenase.

This is part of the hydroxylation rxn in step 2 of the maturation of tropocollagen. Glycosylation won't occur and procollagen won't form.
What causes type VII of Ehlers-Danlos syndrome?
low/no procollagen aminopeptidase (recessive) or mutations in the alpha2(I) gene.

Procollagen won't lose the pro-alpha tails - so NO SELF ASSEMBLY of tropocollagen fibers into collagen.
What bacteria causes gas-gangrene?

Why?
Clostridium Hystolyticum.

It secretes collagenase.
What normal biological function uses collagenase?
The post partum uterus uses collagenase to deconstruct the structures of pregnancy.