量子点
基因组
病毒学
病毒
病毒包膜
生物正交化学
清脆的
传染性
内质网
基因组编辑
生物
纳米技术
计算生物学
材料科学
细胞生物学
化学
遗传学
基因
点击化学
组合化学
作者
Ai-Xin Ma,Cong Yu,Ming‐Yu Zhang,Jian Ao,Haoyang Liu,Meng‐Qian Zhang,Qian-Qian Sun,Dandan Fu,Lei Du,Jing Li,Shu‐Lin Liu,Zhi‐Gang Wang,Dai‐Wen Pang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-02-13
卷期号:24 (8): 2544-2552
被引量:7
标识
DOI:10.1021/acs.nanolett.3c04600
摘要
Labeling the genome and envelope of a virus with multicolor quantum dots (QDs) simultaneously enables real-time monitoring of viral uncoating and genome release, contributing to our understanding of virus infection mechanisms. However, current labeling techniques require genetic modification, which alters the virus's composition and infectivity. To address this, we utilized the CRISPR/Cas13 system and a bioorthogonal metabolic method to label the Japanese encephalitis virus (JEV) genome and envelopes with different-colored QDs in situ. This technique allows one-step two-color labeling of the viral envelope and intraviral genome with QDs harnessing virus infection. In combination with single-virus tracking, we visualized JEV uncoating and genome release in real time near the endoplasmic reticulum of live cells. This labeling strategy allows for real-time visualization of uncoating and genome release at the single-virus level, and it is expected to advance the study of other viral infection mechanisms.
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