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DIGESTION AND ABSORPTION OF
PROTEINS
V.S.RAVIKIRAN, MSc.
V.S.RAVIKIRAN, MSc.,
Department of Biochemistry,
ASRAM Medical college,
Eluru-534005.AP, India.
vsravikiran2013@gmail.com
Action of proteolytic enzymes
Enzyme Hydrolysis of bonds formed by
carboxyl groups of
Pepsin Phe, Tyr, Trp, Met
Trypsin Arg, Lys
Chymotrypsin Phe, Tyr, Trp, Val, Leu
Elastase Ala, Gly, Ser
Carboxypeptidase A C-terminal aromatic amino acids
Caroboxypeptidase B C-terminal basic amino acids
PROTEASES (Peptide hydrolases)
Exopeptidases or peptidases Endopeptidases or proteinases
 Aminopeptidases
 Dipeptidyl peptidases  Serine proteinases (active center has
serine group), e.g. Trypsin
 Tripeptidyl peptidases Cysteine proteinases (active center
has Cysteine group), e.g. Papain
 Carboxypeptidases Aspartic proteinases (active center
has Aspartic group), e.g. Pepsin
 Peptidyl dipeptidases
 Dipeptidases
 Tripeptidases  Metalloproteinase proteinases
(active center has metal group)
 Omega peptidases
(A,V,L I,M.F Y)
(K,R, C)
(D,E)
(P,G)
INTESTINE, BRAIN, KIDNEY TUBULES
NEUTRAL AMINO ACID
Clinical applications:
Abnormalities in protein and amino acids digestion
and absorption:
↓5-oxoprolinase Oxoprolinuria (pyroglutamic
aciduria)
 Partial gastrectomy, pancreatitis, carcinoma of pancreas and cystic
fibrosis (CF)
Protein losing enteropathy
Defects in intestinal amino acid
transport system:
Hartnup’s disease
Imino glycinuria
Cystinuria
Lysinuric protein intoletence
Oasthouse syndrome
Cystinuria:
Intracellular protein degradation:
Cathepsins:
 is a Greek word, meaning ‘to digest’
 present in phagolysosomes
 are 18 in numbers; designated as A-T
 most of them are active around pH 5
 Cathepsin N – collagenolytic cathepsin
 Cathepsin R: degradation of ribosomes
 Cathepsin B: seen extracellularly in pathological conditions
Ubiquitin pathway:
 a 76-residue monomeric protein
 seen in all cells abundantly
 is tag for protein degradation and needs ATP and three enzymes
 Ubiquitin attached proteins are immediately broken down in
proteasomes.
Proteosomes:
 proteasome assembly has a molecular weight of 2000 kD with 28
subunits and has a central cylindrical hollow core.
 Ubiquitin tagged proteins are taken into this barrel, and surrounding
proteolytic enzymes digest the protein into small oligopeptides (5-6
aa).
 Proteosome degradation is also ATP dependent.
Inter-organ Transport of Amino Acids
• Post absorptive (fasting) • After food
Alanine
Glutamine
Valine
Alanine
Glutamine
Alanine
Valine
Brain
Kidney
Muscle
Liver
Gut
THE END
THANKS FORYOUR
ATTENTION

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Digestion and absorption of proteins for Medical School

  • 1. DIGESTION AND ABSORPTION OF PROTEINS V.S.RAVIKIRAN, MSc.
  • 2. V.S.RAVIKIRAN, MSc., Department of Biochemistry, ASRAM Medical college, Eluru-534005.AP, India. vsravikiran2013@gmail.com
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8. Action of proteolytic enzymes Enzyme Hydrolysis of bonds formed by carboxyl groups of Pepsin Phe, Tyr, Trp, Met Trypsin Arg, Lys Chymotrypsin Phe, Tyr, Trp, Val, Leu Elastase Ala, Gly, Ser Carboxypeptidase A C-terminal aromatic amino acids Caroboxypeptidase B C-terminal basic amino acids
  • 9. PROTEASES (Peptide hydrolases) Exopeptidases or peptidases Endopeptidases or proteinases  Aminopeptidases  Dipeptidyl peptidases  Serine proteinases (active center has serine group), e.g. Trypsin  Tripeptidyl peptidases Cysteine proteinases (active center has Cysteine group), e.g. Papain  Carboxypeptidases Aspartic proteinases (active center has Aspartic group), e.g. Pepsin  Peptidyl dipeptidases  Dipeptidases  Tripeptidases  Metalloproteinase proteinases (active center has metal group)  Omega peptidases
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.
  • 18.
  • 19. (A,V,L I,M.F Y) (K,R, C) (D,E) (P,G)
  • 20. INTESTINE, BRAIN, KIDNEY TUBULES NEUTRAL AMINO ACID
  • 21.
  • 22.
  • 23.
  • 24. Clinical applications: Abnormalities in protein and amino acids digestion and absorption: ↓5-oxoprolinase Oxoprolinuria (pyroglutamic aciduria)  Partial gastrectomy, pancreatitis, carcinoma of pancreas and cystic fibrosis (CF) Protein losing enteropathy
  • 25.
  • 26. Defects in intestinal amino acid transport system: Hartnup’s disease Imino glycinuria Cystinuria Lysinuric protein intoletence Oasthouse syndrome
  • 27.
  • 30. Cathepsins:  is a Greek word, meaning ‘to digest’  present in phagolysosomes  are 18 in numbers; designated as A-T  most of them are active around pH 5  Cathepsin N – collagenolytic cathepsin  Cathepsin R: degradation of ribosomes  Cathepsin B: seen extracellularly in pathological conditions
  • 31. Ubiquitin pathway:  a 76-residue monomeric protein  seen in all cells abundantly  is tag for protein degradation and needs ATP and three enzymes  Ubiquitin attached proteins are immediately broken down in proteasomes.
  • 32. Proteosomes:  proteasome assembly has a molecular weight of 2000 kD with 28 subunits and has a central cylindrical hollow core.  Ubiquitin tagged proteins are taken into this barrel, and surrounding proteolytic enzymes digest the protein into small oligopeptides (5-6 aa).  Proteosome degradation is also ATP dependent.
  • 33. Inter-organ Transport of Amino Acids • Post absorptive (fasting) • After food Alanine Glutamine Valine Alanine Glutamine Alanine Valine Brain Kidney Muscle Liver Gut