Wellcome Centre for Anti-Infectives Research, School of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, U.K.
ACS Infect Dis. 2022 Sep 9;8(9):1962-1974. doi: 10.1021/acsinfecdis.2c00364. Epub 2022 Aug 29.
There is a pressing need for new medicines to prevent and treat malaria. Most antimalarial drug discovery is reliant upon phenotypic screening. However, with the development of improved target validation strategies, target-focused approaches are now being utilized. Here, we describe the development of a toolkit to support the therapeutic exploitation of a promising target, lysyl tRNA synthetase (KRS). The toolkit includes resistant mutants to probe resistance mechanisms and on-target engagement for specific chemotypes; a hybrid KRS protein capable of producing crystals suitable for ligand soaking, thus providing high-resolution structural information to guide compound optimization; chemical probes to facilitate pulldown studies aimed at revealing the full range of specifically interacting proteins and thermal proteome profiling (TPP); as well as streamlined isothermal TPP methods to provide unbiased confirmation of on-target engagement within a biologically relevant milieu. This combination of tools and methodologies acts as a template for the development of future target-enabling packages.
迫切需要新的药物来预防和治疗疟疾。大多数抗疟药物的发现都依赖于表型筛选。然而,随着目标验证策略的不断改进,现在正在采用针对目标的方法。在这里,我们描述了一个工具包的开发,以支持对有前途的靶标赖氨酸 tRNA 合成酶(KRS)的治疗性开发。该工具包包括用于探测耐药机制和针对特定化学型的靶标结合的抗性突变体;一种能够产生适合配体浸泡的晶体的杂交 KRS 蛋白,从而提供高分辨率结构信息以指导化合物优化;化学探针可用于进行下拉研究,以揭示特定相互作用蛋白的全部范围和热蛋白质组分析(TPP);以及简化的等温 TPP 方法,可在生物相关环境中提供针对靶标结合的无偏确认。这些工具和方法的组合可作为未来靶标实现包的开发模板。