Identification of the heat shock protein 60 epitope involved in receptor binding on macrophages

被引:22
作者
Habich, C [1 ]
Kempe, K
Burkart, V
van der Zee, R
Lillicrap, M
Gaston, H
Kolb, H
机构
[1] Univ Dusseldorf, Leibniz Inst, Geman Diabet Res Inst, D-40225 Dusseldorf, Germany
[2] Univ Utrecht, Fac Med, Dept Infect Dis & Immunol, NL-3508 TD Utrecht, Netherlands
[3] Univ Cambridge, Dept Med, Cambridge CB2 2QQ, England
关键词
heat shock protein 60; binding epitope; receptor; macrophage;
D O I
10.1016/j.febslet.2004.05.010
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
In the present study, we identified the human beat shock protein 60 (FISP60) epitope responsible for binding to macrophages. Studies using overlapping 15- and 20-mer peptides of the human HSP60 sequence to compete with binding of HSP60 to macrophages indicated that surface binding was accounted for by the region aa481-500. Deletion mutants of FISP60, lacking the N-terminal 137, 243 or 359 amino acids, strongly inhibited HSP60 binding to macrophages. Monoclonal antibodies addressing regions aa1-200, aa335-366 or aa383-447 did not block HSP60 binding. We conclude that a single C-terminal region, aa481-500, accounts for the binding of HSP60 to macrophages. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:65 / 69
页数:5
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