Tanner John D, Richards Sashika N, Corry Ben
Research School of Biology, Australian National University, Canberra, ACT, Australia.
Nat Commun. 2025 Mar 27;16(1):2987. doi: 10.1038/s41467-025-58244-0.
The Plasmodium falciparum chloroquine resistance transporter (PfCRT) is a key protein contributing to resistance against the antimalarial chloroquine (CQ). Mutations such as K76T enable PfCRT to transport CQ away from its target in the parasite's digestive vacuole, but this comes at a cost to its natural peptide transport function. This creates fitness costs which can drive changes to drug susceptibility in parasite populations, but the molecular basis of this is not well understood. To investigate, here we run 130 μs of molecular dynamics simulations of CQ-sensitive and CQ-resistant PfCRT isoforms with CQ and peptide substrates. We identify the CQ binding site and characterized diverse peptide binding modes. The K76T mutation allows CQ to access the binding site but disrupts peptide binding, highlighting the importance of cavity charge in determining substrate specificity. This study provides insight into PfCRT polyspecific peptide transport and will aid in rational, structure-based inhibitor design.
恶性疟原虫氯喹抗性转运蛋白(PfCRT)是导致对抗疟药物氯喹(CQ)产生抗性的关键蛋白。诸如K76T这样的突变使PfCRT能够将氯喹从寄生虫消化泡中的靶点转运走,但这是以其天然的肽转运功能为代价的。这产生了适应性代价,可能会推动寄生虫群体中药物敏感性的变化,但其分子基础尚未得到很好的理解。为了进行研究,我们在此对敏感型和抗性型PfCRT异构体与氯喹和肽底物进行了130微秒的分子动力学模拟。我们确定了氯喹结合位点并表征了多种肽结合模式。K76T突变使氯喹能够进入结合位点,但破坏了肽结合,突出了腔电荷在决定底物特异性方面的重要性。这项研究为PfCRT多特异性肽转运提供了见解,并将有助于基于结构的合理抑制剂设计。