Gupta Priya, Mehrotra Sonali, Sharma Anil, Chugh Monika, Pandey Rajan, Kaushik Abhinav, Khurana Sachin, Srivastava Neha, Srivastava Tarushikha, Deshmukh Arunaditya, Panda Ashutosh, Aggarwal Priyanka, Bhavesh Neel Sarovar, Bhatnagar Raj K, Mohmmed Asif, Gupta Dinesh, Malhotra Pawan
Malaria Biology Group, International Centre for Genetic Engineering and Biotechnology , Aruna Asaf Ali Marg, New Delhi 110067, India.
Translational Bioinformatics Group, International Centre for Genetic Engineering and Biotechnology , Aruna Asaf Ali Marg, New Delhi 110067, India.
J Med Chem. 2017 Oct 26;60(20):8298-8308. doi: 10.1021/acs.jmedchem.7b00089. Epub 2017 Oct 11.
Hemoglobin degradation/hemozoin formation, essential steps in the Plasmodium life cycle, are targets of existing antimalarials. The pathway still offers vast possibilities to be explored for new antimalarial discoveries. Here, we characterize heme detoxification protein, PfHDP, a major protein involved in hemozoin formation, as a novel drug target. Using in silico and biochemical approaches, we identified two heme binding sites and a hemoglobin binding site in PfHDP. Treatment of Plasmodium falciparum 3D7 parasites with peptide corresponding to the hemoglobin binding domain in PfHDP resulted in food vacuole abnormalities similar to that seen with a cysteine protease inhibitor, E-64 (I-1). Screening of compounds that bound the modeled PfHDP structure in the heme/hemoglobin-binding pockets from Maybridge Screening Collection identified a compound, ML-2, that inhibited parasite growth in a dose-dependent manner, thus paving the way for testing its potential as a new drug candidate. These results provide functional insights into the role of PfHDP in Hz formation and further suggest that PfHDP could be an important drug target to combat malaria.
血红蛋白降解/疟原虫色素形成是疟原虫生命周期中的关键步骤,也是现有抗疟药物的作用靶点。该途径仍为新抗疟药物的发现提供了广阔的探索空间。在此,我们将血红素解毒蛋白PfHDP(一种参与疟原虫色素形成的主要蛋白)鉴定为一种新型药物靶点。通过计算机模拟和生化方法,我们在PfHDP中鉴定出两个血红素结合位点和一个血红蛋白结合位点。用与PfHDP中血红蛋白结合域对应的肽处理恶性疟原虫3D7寄生虫,导致食物泡异常,类似于半胱氨酸蛋白酶抑制剂E-64(I-1)所导致的情况。从Maybridge筛选库中筛选与模拟的PfHDP结构在血红素/血红蛋白结合口袋中结合的化合物,鉴定出一种化合物ML-2,它以剂量依赖的方式抑制寄生虫生长,从而为测试其作为新药候选物的潜力铺平了道路。这些结果为PfHDP在疟原虫色素形成中的作用提供了功能见解,并进一步表明PfHDP可能是对抗疟疾的重要药物靶点。