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通过靶向明胶酶 B/基质金属蛋白酶-9(MMP-9)和 TNF-α 转化酶(TACE/ADAM-17)从合成肽文库中定义肽抑制剂。

Definition of peptide inhibitors from a synthetic peptide library by targeting gelatinase B/matrix metalloproteinase-9 (MMP-9) and TNF-α converting enzyme (TACE/ADAM-17).

机构信息

School of Life Science & Technology, China Pharmaceutical University, Nanjing, China.

出版信息

J Enzyme Inhib Med Chem. 2012 Aug;27(4):533-40. doi: 10.3109/14756366.2011.599323. Epub 2011 Aug 10.

Abstract

Gelatinase B/matrix metalloproteinase-9 (MMP-9) is a regulatory and effector metalloproteinase in inflammation. TNF-α is an important proinflammatory cytokine and is released by the action of a Zn(2+)-containing converting enzyme (TACE/ADAM-17). Both metallo-enzymes play important roles during the development of shock syndromes. Combinatorial chemical synthesis and subsequent library deconvolution were previously used to define a peptide inhibitor (Regasepin1) acting, almost to the same degree, on neutrophil collagenase/MMP-8 and MMP-9 in vitro, and protecting mice against lethal endotoxinemia in vivo. We have now extended this approach by incorporating D-form amino acids and residues preferred by TACE. A new peptide library was designed and synthesized, and by deconvolution new peptide inhibitors were defined. These included a TACE-specific inhibitor, an MMP-9- specific inhibitor, and inhibitors for both enzymes.

摘要

明胶酶 B/基质金属蛋白酶-9(MMP-9)是炎症中的一种调节和效应金属蛋白酶。TNF-α 是一种重要的促炎细胞因子,由含有 Zn(2+)的转化酶(TACE/ADAM-17)作用释放。这两种金属酶在休克综合征的发展过程中都起着重要作用。组合化学合成和随后的文库解析以前曾用于定义一种肽抑制剂(Regasepin1),它在体外对中性粒细胞胶原酶/MMP-8 和 MMP-9 的作用几乎相同,并在体内保护小鼠免受致死性内毒素血症的影响。我们现在通过掺入 D 型氨基酸和 TACE 偏好的残基扩展了这种方法。设计并合成了一个新的肽文库,并通过解析定义了新的肽抑制剂。这些抑制剂包括 TACE 特异性抑制剂、MMP-9 特异性抑制剂以及两种酶的抑制剂。

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