ALTERED MOLECULAR-STRUCTURE OF HLA-DR ANTIGENS SYNTHESIZED IN THE PRESENCE OF TUNICAMYCIN

被引:24
作者
NISHIKAWA, Y
YAMAMOTO, Y
ONODERA, K
TAMURA, G
MITSUI, H
机构
[1] TOKYO METROPOLITAN INST MED SCI, 3-18-22 HONKOMAGOME, BUNKYO KU, TOKYO 113, JAPAN
[2] UNIV TOKYO, FAC AGR, DEPT AGR CHEM, BUNKYO KU, TOKYO 113, JAPAN
关键词
D O I
10.1016/S0006-291X(79)80039-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Effects of tunicamycin on the synthesis of proteins and glycoproteins, especially the surface antigens of a human lymphoblastoid cell line (Raji), were investigated. Electrophoretic profiles of [3H]leucine labeled membrane components were similar in the tunicamycin treated cells and untreated cells. However, the respective electrophoretic profiles of [3H]glucosamine labeled membrane components were remarkably different. In the presence of tunicamycin, the relative amount of HLA-DR antigens in the newly synthesized membrane was remarkably reduced, and both subunits of the antigens showed reduced apparent molecular weights. Moreover, one of the subunits completely lost its [3H]glucosamine labeled portion(s), and the other subunit still contained [3H]glucosamine labeled portion(s). These results imply that HLA-DR antigens possess either lipid carrier dependent oligosaccharides or other type(s) of oligosaccharide(s). © 1979 Academic Press, Inc. All rights of reproduction in any form reserved.
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收藏
页码:1235 / 1242
页数:8
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