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
Developmental Therapeutics Program, NCI Frederick, Frederick, Maryland 21702-1201, USA.
Nat Struct Mol Biol. 2004 Jan;11(1):67-72. doi: 10.1038/nsmb711. Epub 2003 Dec 29.
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.
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。