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Analysis of human class I antigens by two-dimensional gel electrophoresis
Authors:Raif G Vasilov  Alfred Hahn  Horst Mölders  Jon J van Rood  Martijn Breuning  Hidde L Ploegh
Institution:(1) Institute for Genetics, University of Cologne, Weyertal 121, D-5000 Cologne 41, Germany;(2) Present address: Shemyakin Institute of Bioorganic Chemistry, USSR Academy of Sciences, 117988 Moscow, USSR;(3) Present address: Dept. of Immunohaematology, Academisch Ziekenhuis Leiden, The Netherlands;(4) Present address: Central Laboratory of the Red Cross Blood Transfusion Service, Amsterdam, The Netherlands
Abstract:Class I antigens were isolated by immunoprecipitation from cell extracts prepared from mitogenically stimulated and internally radiolabeled peripheral blood lymphocytes (PLBs). The precipitating antibodies used are monomorphic and recognize a determinant on the heavy chain of HLA-A, B, C antigens regardless of their allelic specificities when complexed with beta 2m, or determinants on beta 2m itself. Comparison of class I molecules isolated from 25 different homozygous typing cels (HTC) and analyzed by two-dimensional (2-D) gel electrophoresis allowed the identification of those HLA-A,13 locus specificities most common in the European Caucasoid population. Class I antigens isolated from HTC that are HLA identical are biochemically indistinguishable also. Evidence was obtained for the expression of additional class I antigens besides the HLA-A, B, C locus products: for some haplotypes, up to six class I genes may be active in mitogenically activated PBLs. No differences in molecular weight and isoelectric point of the class I heavy chains were observed between the antigens recognized by W6/32, the anti-heavy chain reagent, and anti-beta 2m reagents. The nature of the mitogenic stimulus, i. e., pokeweed mitogen or phytohemagglutinin, was irrelevant with respect to the class I antigens isolated by this method. Using the HTCs as reference, a panel of HLA-B27 positive heterozygous cells was analyzed. Two types of HLA-B27 antigens, distinct by CML typing were represented. These two forms differed also in their biochemical properties. In addition, we obtained evidence for the existence of an A2 variant. This finding was likewise confirmed by CML typing.
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