Co-assembly of HPV capsid proteins and aggregation-induced emission fluorogens for improved cell imaging

Nanoscale. 2020 Mar 7;12(9):5501-5506. doi: 10.1039/c9nr09084c. Epub 2020 Feb 24.

Abstract

In order to improve the cell-imaging ability, and particularly, to extend the bio-application of AIEgen, human papillomavirus (HPV) capsid protein L1 was assembled with the complex of DNA and aggregation-induced emission fluorogen 9,10-distyrylhydrazine (DSAI), where the virus-like particles (VLPs) of HPV encapsulate the complex via electrostatic interaction. The co-assembled nanoparticles, DSAI-DNA@VLPs, showed homogeneous size (∼53 nm), enhanced fluorescence (8 × 2.5-fold), considerable stability (anti-DNase digestion), improved biocompatibility and commendable protection for the DSAI-DNA complex, ensuring virtual brighter imaging in live cells, both for HeLa and normal 293T cell lines.

MeSH terms

  • Capsid Proteins / chemistry*
  • Capsid Proteins / metabolism
  • DNA / chemistry
  • Fluorescent Dyes / chemistry*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Hydrazines / chemistry*
  • Microscopy, Confocal
  • Nanoparticles / chemistry
  • Oncogene Proteins, Viral / chemistry*
  • Oncogene Proteins, Viral / metabolism
  • Particle Size

Substances

  • Capsid Proteins
  • Fluorescent Dyes
  • HPV L1 protein, Human papillomavirus
  • Hydrazines
  • Oncogene Proteins, Viral
  • hydrazine
  • DNA