Literature DB >> 2742594

Use of a novel strategy for the preparation and characterization of an antipeptide antibody capable of recognizing members of the annexin family.

J D Ernst1, E Hoye, R A Blackwood.   

Abstract

Annexins are structurally-related proteins which bind phospholipids in a Ca2+-dependent manner. We have used a novel coupling strategy to prepare an antiserum directed against a 17-amino acid synthetic peptide that resembles the sequence of a highly-conserved portion of these proteins. This antipeptide serum specifically recognizes 5 of 6 human annexins on Western blots, despite differences between the protein and peptide sequences of 3 or 4 amino acids. The antiserum does not recognize endonexin II, whose sequence differs from that of the peptide by 6 amino acids. The availability of multiple proteins with known amino acid sequence has allowed analysis of structural requirements for recognition by this antibody. In some situations, use of such an antibody may allow the identification of a protein as a member of a family.

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Year:  1989        PMID: 2742594     DOI: 10.1016/0006-291x(89)91336-3

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

Review 1.  Annexins: calcium-binding proteins of multi-functional importance?

Authors:  J Römisch; E P Pâques
Journal:  Med Microbiol Immunol       Date:  1991       Impact factor: 3.402

2.  Purification and characterization of an abundant cytosolic protein from human neutrophils that promotes Ca2(+)-dependent aggregation of isolated specific granules.

Authors:  J D Ernst; E Hoye; R A Blackwood; D Jaye
Journal:  J Clin Invest       Date:  1990-04       Impact factor: 14.808

3.  Characterization of Ca2(+)-dependent phospholipid binding, vesicle aggregation and membrane fusion by annexins.

Authors:  R A Blackwood; J D Ernst
Journal:  Biochem J       Date:  1990-02-15       Impact factor: 3.857

  3 in total

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