Solubilization of matrix protein M1/M from virions occurs at different pH for orthomyxo- and paramyxoviruses

Virology. 1990 May;176(1):274-9. doi: 10.1016/0042-6822(90)90253-n.

Abstract

Enveloped viruses, of which the orthomyxo- and paramyxoviruses are members, are known to be uncoated by nonionic detergents in a salt concentration-dependent manner. In this study we have shown that detergent uncoating of myxoviruses depends not only on salt concentration but also on pH. Treatment of orthomyxoviruses with Nonidet-P40 or Triton N-101 at low salt concentrations results in solubilization of surface virion glycopolypeptides in alkaline and neutral pH (9.0-6.5), but in acidic pH (6.0-5.0) the viral matrix protein M1 is also removed, and the viral ribonucleoprotein complex is released. Conversely, the paramyxovirus matrix protein M is more completely solubilized in alkaline pH (pH 9.0) than in neutral and acidic pH 7.4-5.0. The described pH-dependent differences are discussed in terms of orthomyxo- and paramyxovirus uncoating in target cells.

MeSH terms

  • Animals
  • Chickens
  • Glycoproteins / analysis
  • Hydrogen-Ion Concentration
  • Nonoxynol
  • Octoxynol
  • Orthomyxoviridae / isolation & purification*
  • Paramyxoviridae / isolation & purification*
  • Polyethylene Glycols / pharmacology
  • Salts / pharmacology
  • Solubility
  • Viral Matrix Proteins / analysis*
  • Virion / analysis*
  • Virion / drug effects

Substances

  • Glycoproteins
  • Salts
  • Viral Matrix Proteins
  • protein M (glycoprotein)
  • Nonoxynol
  • Polyethylene Glycols
  • Octoxynol
  • Nonidet P-40