Bugge Thomas H, Antalis Toni M, Wu Qingyu
Proteases and Tissue Remodeling Section, NIDCR, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Biol Chem. 2009 Aug 28;284(35):23177-81. doi: 10.1074/jbc.R109.021006. Epub 2009 Jun 1.
Analysis of genome and expressed sequence tag data bases at the turn of the millennium unveiled a new protease family named the type II transmembrane serine proteases (TTSPs) in a Journal of Biological Chemistry minireview (Hooper, J. D., Clements, J. A., Quigley, J. P., and Antalis, T. M. (2001) J. Biol. Chem. 276, 857-860). Since then, the number of known TTSPs has more than doubled, and more importantly, our understanding of the physiological functions of individual TTSPs and their contribution to human disease has greatly increased. Progress has also been made in identifying molecular substrates and endogenous inhibitors. This minireview summarizes the current knowledge of the rapidly advancing TTSP field.
在新千年之交,对基因组和表达序列标签数据库的分析在《生物化学杂志》的一篇小型综述中揭示了一个名为II型跨膜丝氨酸蛋白酶(TTSPs)的新蛋白酶家族(胡珀,J.D.,克莱门茨,J.A.,奎格利,J.P.,和安塔利斯,T.M.(2001年)《生物化学杂志》276,857 - 860)。从那时起,已知的TTSP数量增加了一倍多,更重要的是,我们对单个TTSP的生理功能及其对人类疾病的贡献的理解有了极大的提高。在鉴定分子底物和内源性抑制剂方面也取得了进展。这篇小型综述总结了快速发展的TTSP领域的当前知识。