Chen Liao Y
Department of Physics and Astronomy, The University of Texas at San Antonio, San Antonio, Texas, USA.
Front Phys. 2020 Apr;8. doi: 10.3389/fphy.2020.00119. Epub 2020 Apr 17.
In this article, the Brownian dynamics fluctuation-dissipation theorem (BD-FDT) is applied to the study of transport of neutral solutes across the cellular membrane of Plasmodium berghei (Pb), a disease-causing parasite. Pb infects rodents and causes symptoms in laboratory mice that are comparable to human malaria caused by Plasmodium falciparum (Pf). Due to the relative ease of its genetic engineering, P. berghei has been exploited as a model organism for the study of human malaria. P. berghei expresses one type of aquaporin (AQP), PbAQP, and, in parallel, P. falciparum expresses PfAQP. Either PbAQP or PfAQP is a multifunctional channel protein in the plasma membrane of the rodent/human malarial parasite for homeostasis of water, uptake of glycerol, and excretion of some metabolic wastes across the cell membrane. This FDT-study of the channel protein PbAQP is to elucidate how and how strongly it interacts with water, glycerol, and erythritol. It is found that erythritol, which binds deep inside the conducting pore of PbAQP/PfAQP, inhibits the channel protein's functions of conducting water, glycerol . This points to the possibility that erythritol, a sugar substitute, may inhibit the malarial parasites in rodents and in humans.
在本文中,布朗动力学涨落耗散定理(BD-FDT)被应用于研究中性溶质跨致病寄生虫伯氏疟原虫(Pb)细胞膜的转运。伯氏疟原虫感染啮齿动物,并在实验室小鼠中引发与恶性疟原虫(Pf)引起的人类疟疾相当的症状。由于其基因工程相对容易操作,伯氏疟原虫已被用作研究人类疟疾的模式生物。伯氏疟原虫表达一种水通道蛋白(AQP),即PbAQP,同时,恶性疟原虫表达PfAQP。PbAQP或PfAQP都是啮齿动物/人类疟原虫质膜中的多功能通道蛋白,用于维持水的稳态、摄取甘油以及跨细胞膜排泄一些代谢废物。对通道蛋白PbAQP的这项基于涨落耗散定理的研究旨在阐明它如何以及在多大程度上与水、甘油和赤藓糖醇相互作用。研究发现,结合在PbAQP/PfAQP传导孔深处的赤藓糖醇会抑制通道蛋白传导水、甘油的功能。这表明糖替代品赤藓糖醇可能抑制啮齿动物和人类体内疟原虫的可能性。