首页> 美国卫生研究院文献>Frontiers in Molecular Biosciences >Engagement Rules That Underpin DBL-DARC Interactions for Ingress of Plasmodium knowlesi and Plasmodium vivax Into Human Erythrocytes
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Engagement Rules That Underpin DBL-DARC Interactions for Ingress of Plasmodium knowlesi and Plasmodium vivax Into Human Erythrocytes

机译:参与规则为DBL-DARC交互作用使诺氏疟原虫和间日疟原虫进入人红细胞

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摘要

Malaria parasite erythrocytic stages comprise of repeated bursts of parasites via cyclical invasion of host erythrocytes using dedicated receptor-ligand interactions. A family of erythrocyte-binding proteins from Plasmodium knowlesi (Pk) and Plasmodium vivax (Pv) attach to human Duffy antigen receptor for chemokines (DARC) via their Duffy binding-like domains (DBLs) for invasion. Here we provide a novel, testable and overarching interaction model that rationalizes even contradictory pieces of evidence that have so far existed in the literature on Pk/Pv-DBL/DARC binding determinants. We further address the conundrum of how parasite-encoded Pk/Pv-DBLs recognize human DARC and collate evidence for two distinct DARC integration sites on Pk/Pv-DBLs.
机译:疟疾寄生虫的红细胞生成阶段包括使用专用的受体-配体相互作用,通过周期性侵入宿主红细胞而反复爆发的寄生虫。来自诺氏疟原虫(Pk)和间日疟原虫(Pv)的红细胞结合蛋白家族通过其达菲结合样结构域(DBL)结合到人达菲趋化因子抗原(DARC)上进行侵袭。在这里,我们提供了一种新颖的,可测试的和全面的交互模型,该模型可以合理化迄今为止在Pk / Pv-DBL / DARC结合决定簇文献中存在的甚至相互矛盾的证据。我们进一步解决了寄生虫编码的Pk / Pv-DBL如何识别人DARC并整理Pk / Pv-DBL上两个不同DARC整合位点的证据的难题。

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