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病毒-宿主相互作用中的聚糖:结构视角

Glycans in Virus-Host Interactions: A Structural Perspective.

作者信息

Miller Nathaniel L, Clark Thomas, Raman Rahul, Sasisekharan Ram

机构信息

Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA, United States.

Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, United States.

出版信息

Front Mol Biosci. 2021 Jun 7;8:666756. doi: 10.3389/fmolb.2021.666756. eCollection 2021.

Abstract

Many interactions between microbes and their hosts are driven or influenced by glycans, whose heterogeneous and difficult to characterize structures have led to an underappreciation of their role in these interactions compared to protein-based interactions. Glycans decorate microbe glycoproteins to enhance attachment and fusion to host cells, provide stability, and evade the host immune system. Yet, the host immune system may also target these glycans as glycoepitopes. In this review, we provide a structural perspective on the role of glycans in host-microbe interactions, focusing primarily on viral glycoproteins and their interactions with host adaptive immunity. In particular, we discuss a class of topological glycoepitopes and their interactions with topological mAbs, using the anti-HIV mAb 2G12 as the archetypical example. We further offer our view that structure-based glycan targeting strategies are ready for application to viruses beyond HIV, and present our perspective on future development in this area.

摘要

微生物与其宿主之间的许多相互作用是由聚糖驱动或影响的,聚糖结构的异质性和难以表征导致与基于蛋白质的相互作用相比,人们对其在这些相互作用中的作用认识不足。聚糖修饰微生物糖蛋白以增强与宿主细胞的附着和融合,提供稳定性,并逃避免疫系统。然而,宿主免疫系统也可能将这些聚糖作为糖表位进行靶向。在这篇综述中,我们从结构的角度阐述了聚糖在宿主-微生物相互作用中的作用,主要关注病毒糖蛋白及其与宿主适应性免疫的相互作用。特别是,我们以抗HIV单克隆抗体2G12作为典型例子,讨论了一类拓扑糖表位及其与拓扑单克隆抗体的相互作用。我们进一步认为,基于结构的聚糖靶向策略已准备好应用于除HIV之外的病毒,并提出了我们对该领域未来发展的看法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a56/8215384/142af1df8216/fmolb-08-666756-g001.jpg

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