Proteins Flashcards

(14 cards)

1
Q

What happens to amino acids after absorption?

A

they are now in bloodstream

they are transported to the liver for protein synthesis

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2
Q

Where does protein digestion begin?

A

In the stomach

  • pepsin break down proteins into peptides
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3
Q

What is pepsin?

A

A protease activated in acidic pH that begins protein digestion

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4
Q

Role of pancreatic peptidases

A

Continue protein digestion in the small intestine

e.g. trypsin, chymotrypsin

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5
Q

Role of brush border peptidases

A

Final breakdown of peptides into dipeptides & tripeptides

  • on the apical membrane of enterocytes
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6
Q

How do dipeptides/tripeptides enter enterocytes?

A

Through transporter, called PepT1

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7
Q

What happens to dipeptides/tripeptides once inside enterocytes?

A

Most of them are broken down into smaller constituent amino acids by cytoplasmic peptidases

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8
Q

What is Peptide transporter 1 (PepT1)?

A

A symporter (also called co-transporter)

  • transporting dipeptides/tripeptides from intestinal lumen into enterocytes
    • H⁺ moves against conc. gradient into enterocyte, bringing a dipeptide/tripeptide along with it
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9
Q

Common defective amino acid transport disorders

A
  • Hartnup disease
  • Cystinuria
  • Lysinuric protein intolerance
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10
Q

Consequence of defective amino acid transport

A
  • impaired absorption leading to:

Protein intolerance

Growth retardation

Skeletal & immunological issues

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11
Q

What happens in Hartnup disease?

A

Defect in neutral amino acid transport (e.g. tryptophan)

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12
Q

What happens in Cystinuria?

A

Defect in basic and neutral amino acid transport (e.g. lysine, arginine, cystine)

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13
Q

What happens in Lysinuric protein intolerance?

A

Defect in cationic amino acid transport

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14
Q

Enzymes for protein digestion

A

Pepsin
Pancreatic peptidases
Brush border peptidases
Cytoplasmic peptisases

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