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炭疽致死因子小分子抑制剂的鉴定

Identification of small molecule inhibitors of anthrax lethal factor.

作者信息

Panchal Rekha G, Hermone Ann R, Nguyen Tam Luong, Wong Thiang Yian, Schwarzenbacher Robert, Schmidt James, Lane Douglas, McGrath Connor, Turk Benjamin E, Burnett James, Aman M Javad, Little Stephen, Sausville Edward A, Zaharevitz Daniel W, Cantley Lewis C, Liddington Robert C, Gussio Rick, Bavari Sina

机构信息

Developmental Therapeutics Program, NCI Frederick, Frederick, Maryland 21702-1201, USA.

出版信息

Nat Struct Mol Biol. 2004 Jan;11(1):67-72. doi: 10.1038/nsmb711. Epub 2003 Dec 29.

Abstract

The virulent spore-forming bacterium Bacillus anthracis secretes anthrax toxin composed of protective antigen (PA), lethal factor (LF) and edema factor (EF). LF is a Zn-dependent metalloprotease that inactivates key signaling molecules, such as mitogen-activated protein kinase kinases (MAPKK), to ultimately cause cell death. We report here the identification of small molecule (nonpeptidic) inhibitors of LF. Using a two-stage screening assay, we determined the LF inhibitory properties of 19 compounds. Here, we describe six inhibitors on the basis of a pharmacophoric relationship determined using X-ray crystallographic data, molecular docking studies and three-dimensional (3D) database mining from the US National Cancer Institute (NCI) chemical repository. Three of these compounds have K(i) values in the 0.5-5 microM range and show competitive inhibition. These molecular scaffolds may be used to develop therapeutically viable inhibitors of LF.

摘要

烈性产芽孢细菌炭疽芽孢杆菌分泌由保护性抗原(PA)、致死因子(LF)和水肿因子(EF)组成的炭疽毒素。LF是一种锌依赖性金属蛋白酶,可使关键信号分子(如丝裂原活化蛋白激酶激酶(MAPKK))失活,最终导致细胞死亡。我们在此报告LF小分子(非肽类)抑制剂的鉴定。使用两阶段筛选试验,我们确定了19种化合物的LF抑制特性。在此,我们基于使用X射线晶体学数据、分子对接研究以及从美国国家癌症研究所(NCI)化学储存库进行的三维(3D)数据库挖掘确定的药效关系描述了六种抑制剂。其中三种化合物的K(i)值在0.5 - 5 microM范围内,并表现出竞争性抑制作用。这些分子支架可用于开发具有治疗可行性的LF抑制剂。

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