SYNTHETIC INHIBITORS OF THE MULTICATALYTIC PROTEINASE COMPLEX (PROTEASOME)

被引:59
|
作者
WILK, S
FIGUEIREDOPEREIRA, ME
机构
[1] Department of Pharmacology, Mount Sinai School of Medicine, Box 1215, New York, NY 10029
关键词
MULTICATALYTIC PROTEINASE; PROTEASOME; PEPTIDYL ALDEHYDES; UBIQUITIN;
D O I
10.1159/000468688
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
Synthetic inhibitors of the multicatalytic proteinase complex (proteasome) can provide the means to uncover the functional significance and catalytic mechanism of this macromolecule. Although inhibitor development is still in its early stages, some useful compounds have already been prepared. Of the various types of inhibitors thus far studied, peptidyl aldehydes have been the most effective. Since peptidyl aldehydes inhibit both serine and cysteine proteinases, lack of specificity is their major limitation. The properties of one such compound N-benzyloxycarbonyl-IE(Ot-Bu)A-Leucinal, a potent inhibitor of suc-LLVY-MCA hydrolysis, are described in detail.
引用
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页码:306 / 313
页数:8
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