首页> 外文期刊>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:参与规则的DBL-DARC相互作用为知识性疟原虫和间日疟原虫进入人类红细胞。

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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 P. knowlesi and P. vivax 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通过使用专用受体-配体相互作用周期性地侵入宿主红细胞而反复爆发的寄生虫。来自诺氏假单胞菌和间日疟原虫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受体(DARC),以进行入侵。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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