Subtilase-like pro-protein convertases: from molecular specificity to therapeutic applications

被引:171
作者
Bergeron, F [1 ]
Leduc, R [1 ]
Day, R [1 ]
机构
[1] Univ Sherbrooke, Inst Pharmacol Sherbrooke, Dept Pharmacol, Sherbrooke, PQ J1H 5N4, Canada
关键词
D O I
10.1677/jme.0.0240001
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Limited proteolysis of most large protein precursors is carried out in vivo by the subtilisin-like pro-protein convertases. Many important biological processes such as peptide hormone synthesis, viral protein processing and receptor maturation involve proteolytic processing by these enzymes, making them potential targets for the development of novel therapeutic agents. However, the efficient development of such molecules requires a better understanding of the molecular mechanisms of proteolytic protein processing. Herein, we review the most recent findings on the molecular aspects of subtilisin-like convertase activity, such as the structural analysis of the proteases, the mechanisms of enzyme/substrate specificity, their interaction with other proteins such as 7B2, and the comparative tissue and cellular distribution of the enzymes and their substrates. These data are then used as a background for the review of the known biological functions of subtilisin-like pro-protein convertases, the reported clinical cases involving proteolytic processing defects and, finally, the ongoing development of new therapeutic inhibitor molecules based on this knowledge.
引用
收藏
页码:1 / 22
页数:22
相关论文
共 176 条
[1]
The pore-forming toxin proaerolysin is activated by furin [J].
Abrami, L ;
Fivaz, M ;
Decroly, E ;
Seidah, NG ;
Jean, F ;
Thomas, G ;
Leppla, SH ;
Buckley, JT ;
van der Goot, FG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (49) :32656-32661
[2]
A KEX2-RELATED ENDOPEPTIDASE ACTIVITY PRESENT IN RAT-LIVER SPECIFICALLY PROCESSES THE INSULIN PRORECEPTOR [J].
ALARCON, C ;
CHEATHAM, B ;
LINCOLN, B ;
KAHN, CR ;
SIDDLE, K ;
RHODES, CJ .
BIOCHEMICAL JOURNAL, 1994, 301 :257-265
[3]
Activation of the furin endoprotease is a multiple-step process: Requirements for acidification and internal propeptide cleavage [J].
Anderson, ED ;
VanSlyke, JK ;
Thulin, CD ;
Jean, F ;
Thomas, G .
EMBO JOURNAL, 1997, 16 (07) :1508-1518
[4]
ANDERSON ED, 1993, J BIOL CHEM, V268, P24887
[5]
SYNTHESIS OF TIGHT-BINDING INHIBITORS AND THEIR ACTION ON THE PROPROTEIN-PROCESSING ENZYME FURIN [J].
ANGLIKER, H .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (20) :4014-4018
[6]
Identification of inhibitors of prohormone convertases 1 and 2 using a peptide combinatorial library [J].
Apletalina, E ;
Appel, J ;
Lamango, NS ;
Houghten, RA ;
Lindberg, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (41) :26589-26595
[7]
AYOUBI TAY, 1990, J BIOL CHEM, V265, P15644
[8]
Furilisin: A variant of subtilisin BPN' engineered for cleaving tribasic substrates [J].
Ballinger, MD ;
Tom, J ;
Wells, JA .
BIOCHEMISTRY, 1996, 35 (42) :13579-13585
[9]
Inhibition of proprotein convertases-1, -7 and furin by diterpines of Andrographis paniculata and their succinoyl esters [J].
Basak, A ;
Cooper, S ;
Roberge, AG ;
Banik, UK ;
Chrétien, M ;
Seidah, NG .
BIOCHEMICAL JOURNAL, 1999, 338 :107-113
[10]
BASAK A, 1995, INT J PEPT PROT RES, V46, P228