Department of Biochemistry, Stanford University School of Medicine, Stanford, California, USA.
Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
Antimicrob Agents Chemother. 2024 Aug 7;68(8):e0123823. doi: 10.1128/aac.01238-23. Epub 2024 Jul 22.
We identified MMV026468 as a picomolar inhibitor of blood-stage . Phenotyping assays, including isopentenyl diphosphate rescue of parasite growth inhibition, demonstrated that it targets MEP isoprenoid precursor biosynthesis. MMV026468-treated parasites showed an overall decrease in MEP pathway intermediates, which could result from inhibition of the first MEP enzyme DXS or steps prior to DXS such as regulation of the MEP pathway. Selection of MMV026468-resistant parasites lacking DXS mutations suggested that other targets are possible. The identification of MMV026468 could lead to a new class of antimalarial isoprenoid inhibitors.
我们鉴定出 MMV026468 是一种对血期疟原虫具有皮摩尔级抑制活性的化合物。表型分析实验,包括异戊烯焦磷酸酯对寄生虫生长抑制的挽救实验,证实它靶向于 MEP 异戊烯焦磷酸前体生物合成。用 MMV026468 处理的寄生虫表现出 MEP 途径中间产物的整体减少,这可能是由于对 MEP 途径的第一个酶 DXS 或 DXS 之前的步骤(如 MEP 途径的调控)的抑制所致。对缺乏 DXS 突变的 MMV026468 耐药寄生虫的选择表明可能存在其他靶标。MMV026468 的鉴定可能会导致一类新的抗疟异戊烯焦磷酸酯抑制剂的出现。