Molecular Medicine, Structural Parasitology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, 110067, India.
Department of Medical Elementology and Toxicology, School of Chemical and Life Sciences, Jamia Hamdard, New Delhi, 110062, India.
Nat Commun. 2021 Jan 12;12(1):343. doi: 10.1038/s41467-020-20478-5.
The inhibition of Plasmodium cytosolic phenylalanine tRNA-synthetase (cFRS) by a novel series of bicyclic azetidines has shown the potential to prevent malaria transmission, provide prophylaxis, and offer single-dose cure in animal models of malaria. To date, however, the molecular basis of Plasmodium cFRS inhibition by bicyclic azetidines has remained unknown. Here, we present structural and biochemical evidence that bicyclic azetidines are competitive inhibitors of L-Phe, one of three substrates required for the cFRS-catalyzed aminoacylation reaction that underpins protein synthesis in the parasite. Critically, our co-crystal structure of a PvcFRS-BRD1389 complex shows that the bicyclic azetidine ligand binds to two distinct sub-sites within the PvcFRS catalytic site. The ligand occupies the L-Phe site along with an auxiliary cavity and traverses past the ATP binding site. Given that BRD1389 recognition residues are conserved amongst apicomplexan FRSs, this work lays a structural framework for the development of drugs against both Plasmodium and related apicomplexans.
新型双环氮杂环丁烷抑制疟原虫细胞质苯丙氨酸 tRNA 合成酶(cFRS),具有预防疟疾传播、预防和在疟疾动物模型中提供单剂量治疗的潜力。然而,迄今为止,双环氮杂环丁烷抑制疟原虫 cFRS 的分子基础仍不清楚。在这里,我们提供了结构和生化证据,表明双环氮杂环丁烷是 L-Phe 的竞争性抑制剂,L-Phe 是 cFRS 催化的氨酰基反应所需的三种底物之一,该反应是寄生虫中蛋白质合成的基础。至关重要的是,我们的 PvcFRS-BRD1389 复合物共晶结构显示,双环氮杂环丁烷配体结合到 PvcFRS 催化位点内的两个不同亚位点。配体与辅助腔一起占据 L-Phe 位点,并穿过 ATP 结合位点。鉴于 BRD1389 识别残基在所有顶复体 FRS 中都是保守的,这项工作为开发针对疟原虫和相关顶复体的药物奠定了结构框架。