Literature DB >> 14343122

THE SEQUENTIAL SYNTHESIS OF THE POLYPEPTIDE CHAIN OF SERUM ALBUMIN BY THE MICROSOME FRACTION OF RAT LIVER.

J R SARGENT, P N CAMPBELL.   

Abstract

1. The isolated microsome fraction of regenerating rat liver was incubated with cell sap, a source of energy and [(35)S]methionine, [(14)C]isoleucine or [(14)C]leucine for different periods of time, and microsomal albumin isolated. 2. The distribution of these isotopes in albumin was determined by separation of tryptic peptides from the protein. Radioactivity was measured in peptides either qualitatively by radioautography or quantitatively by labelling with both (3)H and (14)C. 3. A gradient of radioactivity existed at all times in albumin isolated after incubating microsomes. 4. The shorter the incubation time the fewer the peptides labelled in albumin, but the peptides with highest specific activity after short incubation times corresponded to those with highest specific activities after long incubation times. 5. Leucine released from the C-terminus of albumin had a higher specific activity than the mean specific activity of the remaining leucine residues in albumin. 6. The peptide with the highest specific activity in albumin is probably derived from the C-terminus of the protein. 7. [(14)C]Glutamic acid is incorporated into the N-terminus of albumin after incubating the microsome fraction with this isotopically labelled amino acid, cell sap and a source of energy. The specific activity of the N-terminal glutamic acid under these conditions is less than the mean specific activity of the remaining glutamic acid and glutamine residues in albumin. 8. The results are interpreted as reflecting a sequential synthesis of serum albumin in the isolated microsome fraction of rat liver. The direction of synthesis of albumin is from the N-terminus towards the C-terminus. 9. The bulk of incorporation of radioactive amino acid into albumin in the isolated microsome fraction is due to completion of partially completed, pre-existing peptide and polypeptide chains. A limited synthesis of new chains of albumin does, however, occur.

Entities:  

Keywords:  BLOOD PROTEIN ELECTROPHORESIS; DINITROPHENOLS; EXPERIMENTAL LAB STUDY; GLUTAMATES; ISOLEUCINE; LEUCINE; LIVER FUNCTION; METHIONINE; MICROSOMES; PEPTIDES; PROTEIN METABOLISM; RADIOAUTOGRAPHY; RATS; RNA, MESSENGER; SERUM ALBUMIN

Mesh:

Substances:

Year:  1965        PMID: 14343122      PMCID: PMC1206914          DOI: 10.1042/bj0960134

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  27 in total

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5.  The determination of serum albumin and globulin by a new method.

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8.  Studies on the synthesis of serum albumin by ribonucleoprotein particles isolated from rat liver.

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9.  The biosynthesis of rat serum albumin. III. Amino acid composition of rat albumin.

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10.  The terminal peptides of insulin.

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  12 in total

1.  Synthesis of plasma haemopexin, albumin and fibrinogen by the regenerating rat liver.

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2.  Synthesis of a brain-specific protein (S100 protein) in a homologous cell-free system programmed with cerebral polysomal messenger RNA.

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5.  Albumin synthesis by the perfused rat liver. A comparison of methods with special reference to the effect of dietary protein deprivation.

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8.  The effect of age on protein synthesis in mouse liver.

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10.  The effect of 4-dimethylamino-3'-methylazobenzene on 14-C-labelled amino acid incorporation by rat-liver polysome preparations.

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