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. 1985 Jan;82(2):539-42.
doi: 10.1073/pnas.82.2.539.

Human major histocompatibility complex class I antigens: residues 61-83 of the HLA-B7 heavy chain specify an alloreactive site

Human major histocompatibility complex class I antigens: residues 61-83 of the HLA-B7 heavy chain specify an alloreactive site

L E Walker et al. Proc Natl Acad Sci U S A. 1985 Jan.

Abstract

A chemically synthesized peptide (sequence in text) homologous to residues 61-83 of the HLA-B7 heavy chain, induced antibodies that specifically recognized the HLA heavy chain-beta 2-microglobulin complex and the free heavy chain of the HLA-B7 antigen. These antibodies specifically immunoprecipitated the HLA-B7 beta 2-microglobulin complex solubilized from human lymphoblastoid cells by nonionic detergents and reacted with free HLA-B7 heavy chains in blots on nitrocellulose. These observations suggest that the antigenic conformation of this region of the HLA-B7 molecule is independent of the presence of beta 2-microglobulin and that amino acid residues 61-83 mimic an alloreactive site expressed by the HLA-B7 antigen.

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References

    1. J Immunol Methods. 1982;49(1):25-37 - PubMed
    1. Immunogenetics. 1981;13(4):285-95 - PubMed
    1. Proc Natl Acad Sci U S A. 1982 Jun;79(12):3813-7 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Jan;80(1):255-8 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Sep;80(17):5407-11 - PubMed

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