4.6 Article

Role of nuclear localization signals in the DNA delivery function of Chikungunya virus capsid protein

Journal

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 702, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2021.108822

Keywords

Chikungunya virus; Capsid protein; Nuclear localization signal; Nucleic acid-binding domain; Cargo delivery and cellular uptake

Funding

  1. Science and Engineering Research Board (SERB), Department of Science and Technology, Government of India [EMR/2015/001138]
  2. Department of Biotechnology, India

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The study reveals that the capsid of CHIKV has DNA binding and delivery functions in the nucleus, with the NLS1 sequence playing a key role in successful plasmid DNA delivery. The research explores the impact of nonspecific interactions on cellular processes and highlights the significance of Nuclear Localization Signal sequences in the multifunctionality of CHIKV capsid protein.
Capsids of several RNA viruses are reported to have unconventional roles attributed to their subcellular trafficking property. The capsid of CHIKV is also found to localize in the nucleus, but the rationale is not yet clear. To understand the role of the nuclear-localized capsid, we examined the nucleic acid binding and cargo delivery activity of the CHIKV capsid. We used bacterially purified capsid protein to probe the binding affinity with CHIKV genome-specific and non-specific nucleic acids. We found that the capsid was able to bind non-specifically to different forms of nucleic acids. The successful transfection of GFP-tagged plasmid DNA by CHIKV capsid protein shows the DNA delivery ability of the protein. Further, we selected and investigated the DNA binding and cargo delivery activity of commercially synthesized Nuclear Localization Signal sequences (NLS 1 and NLS2) of capsid protein. Both peptides showed comparable DNA binding affinity, however, only the NLS1 peptide was capable of delivering plasmid DNA inside the cell. Furthermore, the cellular uptake study using the FITC-labelled NLS1 peptide was performed to highlight the membrane penetrating ability. Structural analysis was performed using circular dichroism and NMR spectroscopy to elucidate the transfection ability of the NLS1 peptides. Our findings suggest that the capsid of CHIKV might influence cellular trafficking in the infected cell via non-specific interactions. Our study also indicates the significance of NLS sequences in the multifunctionality of CHIKV capsid protein.

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