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金属蛋白酶组织抑制剂突变体作为潜在治疗药物的工程化

Engineering of tissue inhibitor of metalloproteinases mutants as potential therapeutics.

作者信息

Nagase Hideaki, Brew Keith

机构信息

The Kennedy Institute of Rheumatology Division, Faculty of Medicine, Imperial College of Science, Technology and Medicine, London, UK.

出版信息

Arthritis Res. 2002;4 Suppl 3(Suppl 3):S51-61. doi: 10.1186/ar573. Epub 2002 May 9.

Abstract

Matrix metalloproteinases (MMPs) play a central role in many biological processes such as development, morphogenesis and wound healing, but their unbalanced activities are implicated in numerous disease processes such as arthritis, cancer metastasis, atherosclerosis, nephritis and fibrosis. One of the key mechanisms to control MMP activities is inhibition by endogenous inhibitors called tissue inhibitors of metalloproteinases (TIMPs). This review highlights the structures and inhibition mechanism of TIMPs, the biological activities of TIMPs, the unique properties of TIMP-3, and the altered specificity towards MMPs achieved by mutagenesis. A potential therapeutic use of TIMP variants is discussed.

摘要

基质金属蛋白酶(MMPs)在许多生物学过程中发挥着核心作用,如发育、形态发生和伤口愈合,但它们的活性失衡与许多疾病过程有关,如关节炎、癌症转移、动脉粥样硬化、肾炎和纤维化。控制MMP活性的关键机制之一是被称为金属蛋白酶组织抑制剂(TIMPs)的内源性抑制剂的抑制作用。本综述重点介绍了TIMPs的结构和抑制机制、TIMPs的生物学活性、TIMP-3的独特特性以及通过诱变实现的对MMPs特异性的改变。还讨论了TIMP变体的潜在治疗用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33dc/3240149/16970527591d/ar573-1.jpg

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