Salinas Nichole D, Tolia Niraj H
aDepartment of Molecular Microbiology and Microbial Pathogenesis bDepartment of Biochemistry and Molecular Biophysics, Washington University School of Medicine, Saint Louis, Missouri, USA.
Curr Opin Hematol. 2016 May;23(3):215-23. doi: 10.1097/MOH.0000000000000219.
Red cell receptors provide unique entry points for Plasmodium parasites to initiate blood-stage malaria infection. Parasites encode distinct ligands that bind specifically to both highly abundant and low-copy receptors. Recent advances in the understanding of molecular and structural mechanisms of these interactions provide fundamental insights into receptor-ligand biology and molecular targets for intervention.
The review focuses on the requirements for known interactions, insight derived from complex structures, and mechanisms of receptor/ligand engagement. Further, novel roles for established red cell membrane proteins, parasite ligands and associated interacting partners have recently been established in red cell invasion.
The new knowledge underlines the intricacies involved in invasion by a eukaryotic parasite into a eukaryotic host cell demonstrated by expanded parasite ligand families, redundancy in red cell receptor engagement, multitiered temporal binding, and the breadth of receptors engaged.
红细胞受体为疟原虫启动血液阶段疟疾感染提供了独特的切入点。疟原虫编码不同的配体,这些配体特异性结合高丰度和低拷贝受体。对这些相互作用的分子和结构机制理解的最新进展为受体-配体生物学和干预的分子靶点提供了基本见解。
本综述重点关注已知相互作用的要求、从复杂结构中获得的见解以及受体/配体结合的机制。此外,已确定的红细胞膜蛋白、寄生虫配体和相关相互作用伙伴在红细胞入侵中最近有了新的作用。
新知识强调了真核寄生虫侵入真核宿主细胞所涉及的复杂性,这体现在寄生虫配体家族的扩展、红细胞受体结合的冗余性、多层次的时间结合以及所涉及受体的广度上。