4.8 Article

Intracellular self-assembly based multi-labeling of key viral components: Envelope, capsid and nucleic acids

Journal

BIOMATERIALS
Volume 99, Issue -, Pages 24-33

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2016.04.038

Keywords

Viral components; Multi-labeling; Intracellular self-assembly; Infectivity; Real-time monitoring

Funding

  1. National Basic Research Program of China (973 Program) [2011CB933600]
  2. National Natural Science Foundation of China [21275111, 21535005]
  3. 111 Project [111-2-10]
  4. China Scholarship Council [201406275115]
  5. Collaborative Innovation Center for Chemistry and Molecular Medicine

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Envelope, capsid and nucleic acids are key viral components that are all involved in crucial events during virus infection. Thus simultaneous labeling of these key components is an indispensable prerequisite for monitoring comprehensive virus infection process and dissecting virus infection mechanism. Baculovirus was genetically tagged with biotin on its envelope protein GP64 and enhanced green fluorescent protein (EGFP) on its capsid protein VP39. Spodoptera frugiperda 9 (Sf9) cells were infected by the recombinant baculovirus and subsequently fed with streptavidin-conjugated quantum dots (SA-QDs) and cell permeable nucleic acids dye SYTO 82. Just by genetic engineering and virus propagation, multi labeling of envelope, capsid and nucleic acids was spontaneously accomplished during virus inherent self-assembly process, significantly simplifying the labeling process while maintaining virus infectivity. Intracellular dissociation and transportation of all the key viral components, which was barely reported previously, was real-time monitored based on the multi-labeling approach, offering opportunities for deeply understanding virus infection and developing anti-virus treatment. (C) 2016 Elsevier Ltd. All rights reserved.

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