Encapsulating Quantum Dots within HIV-1 Virions through Site-Specific Decoration of the Matrix Protein Enables Single Virus Tracking in Live Primary Macrophages
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时间:2020-05-15
Encapsulating Quantum Dots within HIV-1 Virions through Site-Specific Decoration of the Matrix Protein Enables Single Virus Tracking in Live Primary Macrophages
Li, Q., W. Yin, W. Li, Z. Zhang, X. Zhang, X.-E. Zhang and Z. Cui
Nano Lett.2018 Dec 12;18(12):7457-7468. doi: 10.1021/acs.nanolett.8b02800. Epub 2018 Nov 8.
Abstract
Labeling and imaging withquantumdots (QDs) provides powerful tools to visualize viral infection in living cells.Encapsulating QDs withinvirionsrepresents a novel strategy forvirus labeling. Here, we developed infectiousHIV-1virionsencapsulating QDs throughsite-specificdecoration of the viralmatrixprotein (MA) and used them to visualize early infection events in humanprimarymacrophages bysingle-particle imaging. The MAproteinwas fused to a biotin acceptor peptide (BAP) tag, biotinylated, complexed with streptavidin-conjugated QDs inlive cells, and incorporated intovirions duringvirus assembly. The QD-encapsulatedvirions were tracked during infection ofmacrophages at asingle particle level. The dynamic dissociation of MA and Vpr was also tracked in real time, and the results demonstrated that MA has multiple dynamic behaviors and functions duringvirus entry. More importantly, we tracked the dynamic interplay of QD-encapsulatedvirions with cellular mitochondria inliveprimarymacrophages. We also found thatHIV-1 can induce fission of mitochondria during the early phases of infection. In summary, we have constructed a type of QD-encapsulatedvirus particle and used this technology to further our understanding of the early events ofHIV-1 infection.
科研成果