Viral capsid mobility: a dynamic conduit for inactivation

Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2274-7. doi: 10.1073/pnas.051598298. Epub 2001 Feb 13.

Abstract

Mass spectrometry and fluorescent probes have provided direct evidence that alkylating agents permeate the protein capsid of naked viruses and chemically inactivate the nucleic acid. N-acetyl-aziridine and a fluorescent alkylating agent, dansyl sulfonate aziridine, inactivated three different viruses, flock house virus, human rhinovirus-14, and foot and mouth disease virus. Mass spectral studies as well as fluorescent probes showed that alkylation of the genome was the mechanism of inactivation. Because particle integrity was not affected by selective alkylation (as shown by electron microscopy and sucrose gradient experiments), it was reasoned that the dynamic nature of the viral capsid acts as a conduit to the interior of the particle. Potential applications include fluorescent labeling for imaging viral genomes in living cells, the sterilization of blood products, vaccine development, and viral inactivation in vivo.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Aphthovirus / drug effects*
  • Aphthovirus / physiology
  • Aziridines / pharmacology
  • Capsid / chemistry
  • Capsid / physiology*
  • Drosophila melanogaster
  • Mechlorethamine / pharmacology
  • RNA Viruses / drug effects*
  • RNA Viruses / physiology
  • Rhinovirus / drug effects*
  • Rhinovirus / physiology
  • Spectrometry, Mass, Electrospray Ionization / methods

Substances

  • Aziridines
  • Mechlorethamine