LEUKOCYTE GELATINASE-B CLEAVAGE RELEASES ENCEPHALITOGENS FROM HUMAN MYELIN BASIC-PROTEIN

被引:165
作者
PROOST, P
VANDAMME, J
OPDENAKKER, G
机构
[1] The Rega Institute for Medical Research, University of Leuven, B-3000 Leuven
关键词
D O I
10.1006/bbrc.1993.1540
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
Gelatinase B, a marker enzyme for chronic inflammatory diseases such as rheumatoid arthritis and multiple sclerosis (MS), was found to cleave human myelin basic protein (MBP). Human MBP was digested with gelatinase B from leukocytes. The MBP peptide fragments were separated by RP-HPLC and the gelatinase B cleavage sites established by aminoterminal sequence analysis. Several novel P1-P1′ cleavage sites for gelatinase B were found. The positions of the cleavage sites in human MBP were such that at least one peptide coincided with a documented major MBP-autoantigen. This study annotates human MBP as a substrate for human gelatinase B, determines novel P1-P′1 cleavage sites and defines one of the metalloproteinases as a possible link in the pathogenesis of demyelinating diseases such as MS. © 1993 Academic Press. All rights reserved.
引用
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页码:1175 / 1181
页数:7
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