Literature DB >> 6785233

Synthesis and biological assays of a peptide from a tuberculin-active protein.

J Savrda.   

Abstract

The heptapeptide Asn-Gly-Ser-Gln-Met-Arg-Leu, part of a tuberculin-active intracellular mycobacterial protein and described in the literature as having residual tuberculin activity, has been synthesized. Biological assays of the synthetic peptide showed it to be recognized as an antigen of mycobacterial origin by its ability to elicit an early allergic reaction in Mycobacterium bovis BCG-infected mice. The synthetic peptide was shown to be devoid of any tuberculin activity in BCG-infected mice and in skin tests on Mycobacterium tuberculosis-sensitized guinea pigs. Purified protein derivative, complex mixture of proteins of unknown composition which is excreted into the culture medium by M. tuberculosis and is in wide use as a tuberculin-active preparation, was shown to weakly cross-react in radioimmunoassays with the synthetic heptapeptide when 125I-labeled heptapeptide and an anti-heptapeptide antiserum were used.

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Year:  1980        PMID: 6785233      PMCID: PMC551370          DOI: 10.1128/iai.30.3.686-693.1980

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  12 in total

1.  Minimal structural requirements for adjuvant activity of bacterial peptidoglycan derivatives.

Authors:  F Ellouz; A Adam; R Ciorbaru; E Lederer
Journal:  Biochem Biophys Res Commun       Date:  1974-08-19       Impact factor: 3.575

2.  Revised amide location for porcine and human adrenocorticotropic hormone.

Authors:  L Gráf; S Bajusz; A Patthy; E Barát; G Cseh
Journal:  Acta Biochim Biophys Acad Sci Hung       Date:  1971

3.  Removal of the N alpha-benzyloxycarbonyl group from cysteine-containing peptides by catalytic hydrogenolysis in liquid ammonia, exemplified by a synthesis of oxytocin.

Authors:  K Kuromizu; J Meienhofer
Journal:  J Am Chem Soc       Date:  1974-07-24       Impact factor: 15.419

4.  Boron tris(trifluoroacetate) for removal of protecting groups in peptide chemistry.

Authors:  J Pless; W Bauer
Journal:  Angew Chem Int Ed Engl       Date:  1973-02       Impact factor: 15.336

5.  [Analysis by polyacrylamide gel isoelectric focusing of protein fractions present in the purified protein derivatives (PPD)].

Authors:  J Augier; S Augier-Gibory
Journal:  Ann Inst Pasteur (Paris)       Date:  1969-12

6.  [A new method for synthesis of peptides: activation of the carboxyl group with dicyclohexylcarbodiimide using 1-hydroxybenzotriazoles as additives].

Authors:  W König; R Geiger
Journal:  Chem Ber       Date:  1970

7.  A new method for releasing oxytocin from fully-protected nona-peptides using anhydrous hydrogen fluoride.

Authors:  S Sakakibara; Y Shimonishi
Journal:  Bull Chem Soc Jpn       Date:  1965-08       Impact factor: 5.488

8.  Purification and properties of tuberculin-active protein from Mycobacterium tuberculosis.

Authors:  S Kuwabara
Journal:  J Biol Chem       Date:  1975-04-10       Impact factor: 5.157

9.  Electrophoretic mobilities of peptides on paper and their use in the determination of amide groups.

Authors:  R E Offord
Journal:  Nature       Date:  1966-08-06       Impact factor: 49.962

10.  The labelling of proteins to high specific radioactivities by conjugation to a 125I-containing acylating agent.

Authors:  A E Bolton; W M Hunter
Journal:  Biochem J       Date:  1973-07       Impact factor: 3.857

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  2 in total

1.  Synthesis and biological assays of peptides from a tuberculin-active protein.

Authors:  J Savrda
Journal:  Infect Immun       Date:  1983-06       Impact factor: 3.441

2.  A chemically synthesized peptide which elicits humoral and cellular immune responses to mycobacterial antigens.

Authors:  P Minden; R A Houghten; J R Spear; T M Shinnick
Journal:  Infect Immun       Date:  1986-09       Impact factor: 3.441

  2 in total

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