参与宿主红细胞膜营养通道的疟原虫蛋白:研究进展及未来研究问题。

International journal of current multidisciplinary studies Pub Date : 2017-03-01 Epub Date: 2017-03-28
S Chalapareddy, S A Desai
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引用次数: 0

摘要

感染疟疾寄生虫的红细胞对营养物质和其他溶质的渗透性增加,这是由一种称为疟原虫表面阴离子通道(PSAC)的不寻常离子通道介导的。尽管感染红细胞通透性增加在70多年前就已被发现,并随后通过示踪剂研究进行了表征,但直到膜片钳方法和高通量筛选技术的引入,其在寄生虫生物学中的机制和作用仍不清楚。这些方法发现并暗示PSAC是主要机制,确定了该通道对寄生虫发育至关重要,导致了通道基因的鉴定,并刺激了针对该靶点的抗疟疾药物的发现。尽管取得了这些进展,但关于这种不寻常的寄生虫通道仍存在许多问题。我们的综述强调了一些最近的进展,并描述了未来研究的重要问题。
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Malaria parasite proteins involved in nutrient channels at the host erythrocyte membrane: advances and questions for future research.

Erythrocytes infected malaria parasites have increased permeability to nutrients and other solutes, as mediated by an unusual ion channel known as the plasmodial surface anion channel (PSAC). Although the increased permeability of infected erythrocytes was identified more than 70 years ago and subsequently characterized with tracer studies, its mechanism and role in parasite biology remained unclear until the introduction of patch-clamp methods and high-throughput screening technologies. These methods discovered and implicated PSAC as the primary mechanism, determined that this channel is essential for parasite development, led to identification of the channel's genes, and stimulated antimalarial drug discovery against this target. Despite these advances, many questions remain about this unusual parasite channel. Our review highlights some recent advances and describes important questions for future research.

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