Does Plasmodium falciparum have an Achilles' heel?

Liao Y Chen
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引用次数: 5

Abstract

Background: Plasmodium falciparum is the parasite that causes the most severe form of malaria responsible for nearly a million deaths a year. Currently, science has been established about its cellular structures, its metabolic processes, and even the molecular structures of its intrinsic membrane proteins responsible for transporting water, nutrient, and waste molecules across the parasite plasma membrane (PPM).

Presentation of the hypothesis: I hypothesize that Plasmodium falciparum has an Achilles' heel that can be attacked with erythritol, the well-known sweetener that is classified as generally safe. This hypothesis is based on the molecular structure of the parasite's membrane and the quantitative mechanics of how erythritol interacts with the multi-functional channel protein expressed in the PPM. Most organisms have in their cell membrane two types of water-channel proteins: aquaporins to maintain hydro-homeostasis across the membrane and aquaglyceroporins to uptake glycerols etc. In contrast, P. falciparum has only one type of such proteins---the multi-functional aquaglyceroporin (PfAQP) expressed in the PPM---to do both jobs. Moreover, the parasite also uses PfAQP to excrete its metabolic wastes (ammonia included) produced at a very high rate in the blood stage. This extremely high efficiency of the bug using one protein for multiple essential tasks makes the parasite fatally vulnerable. Erythritol in the blood stream can kill the parasite by clogging up its PfAQP channel that needs to be open for maintaining hydro-homeostasis and for excreting toxic wastes across the bug's PPM.

Testing the hypothesis: In vitro tests are to measure the growth/death rate of P. falciparum in blood with various erythritol concentrations. In vivo experiments are to administer groups of infected mice with various doses of erythritol and monitor the parasite growth levels from blood samples drawn from each group. Clinic trials can be performed to observe the added effects of administering to patients erythritol along with the known drugs because erythritol was classified as a safe food ingredient.

Implications of the hypothesis: If proven true, erythritol will cure the most severe form of malaria without significant side effects.

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恶性疟原虫有致命弱点吗?
背景:恶性疟原虫是引起最严重形式疟疾的寄生虫,每年造成近100万人死亡。目前,科学已经建立了它的细胞结构,它的代谢过程,甚至它的内在膜蛋白的分子结构,负责在寄生虫的质膜(PPM)上运输水,营养物质和废物分子。假设陈述:我假设恶性疟原虫有一个致命的弱点,可以用赤藓糖醇来攻击,赤藓糖醇是一种众所周知的被归类为一般安全的甜味剂。这一假设是基于寄生虫膜的分子结构和赤藓糖醇如何与PPM中表达的多功能通道蛋白相互作用的定量机制。大多数生物体的细胞膜上都有两种类型的水通道蛋白:水通道蛋白(用于维持细胞膜上的水稳态)和水甘油孔蛋白(用于摄取甘油等)。相比之下,恶性疟原虫只有一种这样的蛋白质——在PPM中表达的多功能水甘油三酯oporin (PfAQP)——来完成这两项工作。此外,寄生虫还利用PfAQP排泄其在血液阶段以非常高的速率产生的代谢废物(包括氨)。这种利用一种蛋白质完成多种基本任务的极高效率使得寄生虫极易受到致命的攻击。血液中的赤藓糖醇可以通过堵塞PfAQP通道来杀死寄生虫,而PfAQP通道需要打开,以维持水稳态,并通过细菌的PPM排出有毒废物。检验假设:体外试验是测量不同赤藓糖醇浓度的血液中恶性疟原虫的生长/死亡率。体内实验是给感染小鼠注射不同剂量的赤藓糖醇,并从每组小鼠的血液样本中监测寄生虫的生长水平。临床试验可以观察给病人服用赤藓糖醇和已知药物的附加效果因为赤藓糖醇被列为安全的食品成分。假设的含义:如果证明是正确的,赤藓糖醇将治愈最严重形式的疟疾而没有明显的副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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