Single-Particle Tracking Reveals the Interplay between HIV-1 Reverse Transcription and Uncoating

被引:4
|
作者
Ma, Yingxin [1 ]
Mao, Guobin [1 ]
Wu, Guoqiang [1 ]
Zhang, Xian-En [2 ,3 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Synthet Biol, Shenzhen Inst Adv Technol, CAS Key Lab Quantitat Engn Biol, Shenzhen 518055, Peoples R China
[2] Chinese Acad Sci, Fac Synthet Biol, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
[3] Chinese Acad Sci, Natl Key Lab Biomacromol, Inst Biophys, Beijing 100101, Peoples R China
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; CORE; RESTRICTION; TRIM5-ALPHA; INHIBITION; STABILITY;
D O I
10.1021/acs.analchem.1c05199
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Reverse transcription uses the reverse transcriptase enzyme to synthesize deoxyribonucleic acid (DNA) from a ribonucleic acid (RNA) template. This plays an essential role in viral replication. There are still, however, many unknown facts regarding the timing and dynamic processes involved in this life stage. Here, three types of dual-fluorescence human immunodeficiency virus type-1 (HIV-1) particles were constructed with high infectivity, and the sequential process of reverse transcription was observed by real-time imaging of a single HIV-1 particle. Viral uncoating occurred at 60-120 min post infection. Subsequently, at 120-180 min post infection, the viral genome was separated into two parts and reverse-transcribed to generate a DNA product. Nevirapine (NVP), a reverse transcriptase inhibitor, can delay the dynamic process. This study revealed a delicate, sequential, and complex relationship between uncoating and reverse transcription, which may facilitate the development of antiviral drugs.
引用
收藏
页码:2648 / 2654
页数:7
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