L 23 Flashcards

(13 cards)

1
Q

How are N linked oligosaccharids added in the ER?

A

by block transfer as it travels from the ER to the golgi

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2
Q

Where does the O linked glycosylation occur?

A

In the golgi

  1. occurs on the OH group of Ser or Thr
  2. Occurs on completed polypeptide chains
  3. occurs by the serial addition of single monosaccharide units
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3
Q

N linked glycosylation occurs where?

A

in the ER and golgi

  1. occurs on NH2 group of Asn in the N-X-S/T sequence motif
  2. occurs cotranslationally at the ER part
  3. occurs by block transfer of a 14 residue core oligosaccharide in the Er, then trimmed and modified further in the Er and golgi but always retain same 5 residue core pentasaccharide
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4
Q

Where are the sugars being added on to oligosaccharides from?

A

they are added from nucleotide sugar donors.

activating the sugar provides the NRG to form glycosidic bond

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5
Q

during synthesis of o linked oligosaccharide, most glycosidic bonds require what?

A

a specific glycosyltransferase

there’s hundreds in the human genome

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6
Q

N linked oligosaccharides are synthesized on what?

A

dolichol

it’s synthesized in a way that’s similar to cholesterol pathway

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7
Q

What’s interesting about the formation of core oligosaccharide on dolichol phosphate?

A

it starts in the cytosol and is completed in the ER lumen

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8
Q

What are some functions of glycosylation? 3

A
  1. recognition - sperm-egg, white blood cell adhesion during inflammation response, bacterial and viral invasion of cells
  2. Targeting - lysosome targeting signal is mannose 6 phosphate
  3. antigens -ABO group
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9
Q

What does EPO stand for?

A

erythropoeitin

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10
Q

What exactly is erythropoietin?

A

a glycoprotein hormone secreted from the kidneys

40% carbohydrate by weight

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11
Q

What does EPO stimulate?

A

It stimulates the production of red blood cells

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12
Q

What can EPO be used to treat?

A

To treat anemia, esp during chemotherpay and depended on avilability ofrecombinant human EPO

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13
Q

How is I cell disease caused?

A

Caused by defect in lysosomal targeting

  • many hydrolytic enzymes fail to be targeted to lysosomes and secreted from cells
  • average lifespan is about 8 years
  • skeletal abnormalities, psychomotor retardation
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