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点击病毒——借助化学方法探索感染机制

Clicking viruses-with chemistry toward mechanisms in infection.

作者信息

Greber Urs F

机构信息

Department of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.

出版信息

J Virol. 2025 Jun 17;99(6):e0047125. doi: 10.1128/jvi.00471-25. Epub 2025 May 14.

DOI:10.1128/jvi.00471-25
PMID:40366176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12172498/
Abstract

Viruses subvert cells and evade host defense. They emerge unpredictably and threaten humans and livestock through their genetic and phenotypic diversity. Despite more than 100 years since the discovery of viruses, the molecular underpinnings of virus infections are incompletely understood. The introduction of new methodologies into the field, such as that of click chemistry some 10 years ago, keeps uncovering new facets of viruses. Click chemistry uses bio-orthogonal reactions on chemical probes and couples nucleic acids, proteins, and lipids with tractable labels, such as fluorophores for single-cell and single-molecule imaging, or biotin for biochemical profiling of infections. Its applications in single cells often achieve single-molecule resolution and provide important insights into the widely known phenomenon of cell-to-cell infection variability. This review describes click chemistry advances to unravel infection mechanisms of a select set of enveloped and nonenveloped DNA and RNA viruses, including adenovirus, herpesvirus, and human immunodeficiency virus. It highlights recent click chemistry breakthroughs with viral DNA, viral RNA, protein, as well as host-derived lipid functions in both live and chemically fixed cells. It discusses new insights on specific processes including virus entry, uncoating, transcription, replication, packaging, and assembly and provides a perspective for click chemistry to explore viral cell biology, infection variability, and genome organization in the particle.

摘要

病毒会颠覆细胞并逃避宿主防御。它们以不可预测的方式出现,并通过其遗传和表型多样性威胁人类和牲畜。尽管自病毒发现以来已有100多年,但对病毒感染的分子基础仍未完全了解。大约10年前将点击化学等新方法引入该领域,不断揭示病毒的新面貌。点击化学利用化学探针上的生物正交反应,将核酸、蛋白质和脂质与易于处理的标记物偶联,例如用于单细胞和单分子成像的荧光团,或用于感染生化分析的生物素。其在单细胞中的应用通常能达到单分子分辨率,并为广为人知的细胞间感染变异性现象提供重要见解。本综述描述了点击化学在揭示一组有包膜和无包膜的DNA和RNA病毒(包括腺病毒、疱疹病毒和人类免疫缺陷病毒)感染机制方面的进展。它强调了近期在活细胞和化学固定细胞中点击化学在病毒DNA、病毒RNA、蛋白质以及宿主衍生脂质功能方面的突破。它讨论了对包括病毒进入、脱壳、转录、复制、包装和组装等特定过程的新见解,并为点击化学探索病毒细胞生物学、感染变异性以及病毒颗粒中的基因组组织提供了一个视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/f8265fc59e7e/jvi.00471-25.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/209c8a54aa06/jvi.00471-25.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/fee4a5615923/jvi.00471-25.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/f5a0fd4dbc8c/jvi.00471-25.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/f8265fc59e7e/jvi.00471-25.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/209c8a54aa06/jvi.00471-25.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/fee4a5615923/jvi.00471-25.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/f5a0fd4dbc8c/jvi.00471-25.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5065/12172498/f8265fc59e7e/jvi.00471-25.f004.jpg

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