Van Voorhis Wesley C, Doggett J Stone, Parsons Marilyn, Hulverson Matthew A, Choi Ryan, Arnold Samuel L M, Riggs Michael W, Hemphill Andrew, Howe Daniel K, Mealey Robert H, Lau Audrey O T, Merritt Ethan A, Maly Dustin J, Fan Erkang, Ojo Kayode K
Department of Medicine, Division of Allergy and Infectious Diseases, Center for Emerging and Reemerging Infectious Diseases (CERID), University of Washington, Seattle, WA 98109, USA; Department of Global Health, University of Washington, Seattle, WA 98195, USA.
Portland VA Medical Center, Portland, OR 97239, USA.
Exp Parasitol. 2017 Sep;180:71-83. doi: 10.1016/j.exppara.2017.01.001. Epub 2017 Jan 5.
Many life-cycle processes in parasites are regulated by protein phosphorylation. Hence, disruption of essential protein kinase function has been explored for therapy of parasitic diseases. However, the difficulty of inhibiting parasite protein kinases to the exclusion of host orthologues poses a practical challenge. A possible path around this difficulty is the use of bumped kinase inhibitors for targeting calcium-dependent protein kinases that contain atypically small gatekeeper residues and are crucial for pathogenic apicomplexan parasites' survival and proliferation. In this article, we review efficacy against the kinase target, parasite growth in vitro, and in animal infection models, as well as the relevant pharmacokinetic and safety parameters of bumped kinase inhibitors.
寄生虫的许多生命周期过程都受蛋白质磷酸化调控。因此,人们探索通过破坏必需蛋白激酶的功能来治疗寄生虫病。然而,在抑制寄生虫蛋白激酶而不影响宿主同源物方面存在困难,这构成了一项实际挑战。解决这一困难的一条可能途径是使用碰撞激酶抑制剂来靶向钙依赖性蛋白激酶,这些激酶含有非典型的小守门残基,对致病性顶复门寄生虫的生存和增殖至关重要。在本文中,我们综述了碰撞激酶抑制剂对激酶靶点的疗效、体外寄生虫生长情况以及在动物感染模型中的表现,以及相关的药代动力学和安全性参数。