Development of Toxoplasma gondii Calcium-Dependent Protein Kinase 1 (TgCDPK1) Inhibitors with Potent Anti-Toxoplasma Activity

被引:91
作者
Johnson, Steven M. [2 ]
Murphy, Ryan C. [2 ]
Geiger, Jennifer A. [4 ]
DeRocher, Amy E. [4 ]
Zhang, Zhongsheng [3 ]
Ojo, Kayode K. [1 ]
Larson, Eric T. [3 ]
Perera, B. Gayani K. [2 ]
Dale, Edward J. [2 ]
He, Panqing [1 ]
Reid, Molly C. [1 ]
Fox, Anna M. W. [1 ]
Mueller, Natascha R. [1 ]
Merritt, Ethan A. [3 ]
Fan, Erkang [3 ]
Parsons, Marilyn [4 ,5 ]
Van Voorhis, Wesley C. [1 ,5 ]
Maly, Dustin J. [2 ]
机构
[1] Univ Washington, Dept Med, Div Allergy & Infect Dis, Seattle, WA 98105 USA
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[3] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[4] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[5] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
关键词
UNITED-STATES; INFECTION; DISCOVERY; ANIMALS; HUMANS;
D O I
10.1021/jm201713h
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Toxoplasmosis is a disease of prominent health concern that is caused by the protozoan parasite Toxoplasma gondii. Proliferation of T. gondii is dependent on its ability to invade host cells, which is mediated in part by calcium-dependent protein kinase 1 (CDPK1). We have developed ATP competitive inhibitors of TgCDPK1 that block invasion of parasites into host cells, preventing their proliferation. The presence of a unique glycine gatekeeper residue in TgCDPK1 permits selective inhibition of the parasite enzyme over human kinases. These potent TgCDPK1 inhibitors do not inhibit the growth of human cell lines and represent promising candidates as toxoplasmosis therapeutics.
引用
收藏
页码:2416 / 2426
页数:11
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