Sullivan D J, Gluzman I Y, Russell D G, Goldberg D E
Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, MO USA.
Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11865-70. doi: 10.1073/pnas.93.21.11865.
Chloroquine is thought to exert its antimalarial effect by preventing the polymerization of toxic heme released during proteolysis of hemoglobin in the Plasmodium digestive vacuole. The mechanism of this blockade has not been established. We incubated cultured parasites with subinhibitory doses of [3H]chloroquine and [3H] quinidine. These [3H]quinoline compounds became associated with hemozoin as assessed by electron microscope autoradiography and subcellular fractionation. In vitro, binding of [3H]quinoline inhibitors to the hemozoin chain depended on the addition of heme substrate. These data counter previous conclusions regarding the lack of quinoline association with hemozoin, explain the exaggerated accumulation of quinolines in the plasmodium digestive vacuole, and suggest that a quinoline heme complex incorporates into the growing polymer to terminate chain extension, blocking further sequestration of toxic heme.
氯喹被认为是通过阻止疟原虫消化泡内血红蛋白蛋白水解过程中释放的有毒血红素的聚合来发挥其抗疟作用的。这种阻断的机制尚未明确。我们用亚抑制剂量的[3H]氯喹和[3H]奎尼丁培养寄生虫。通过电子显微镜放射自显影和亚细胞分级分离评估,这些[3H]喹啉化合物与疟色素相关。在体外,[3H]喹啉抑制剂与疟色素链的结合取决于血红素底物的添加。这些数据反驳了之前关于喹啉与疟色素缺乏关联的结论,解释了喹啉在疟原虫消化泡中过度积累的现象,并表明喹啉 - 血红素复合物并入正在生长的聚合物中以终止链延伸,从而阻止有毒血红素的进一步隔离。