Alleviation of a defect in protein folding by increasing the rate of subunit assembly

J Biol Chem. 2001 Jul 6;276(27):25372-7. doi: 10.1074/jbc.M101759200. Epub 2001 Apr 13.

Abstract

Understanding the nature of protein grammar is critical because amino acid substitutions in some proteins cause misfolding and aggregation of the mutant protein resulting in a disease state. Amino acid substitutions in phage P22 coat protein, known as tsf (temperature-sensitive folding) mutations, cause folding defects that result in aggregation at high temperatures. We have isolated global su (suppressor) amino acid substitutions that alleviate the tsf phenotype in coat protein (Aramli, L. A., and Teschke, C. M. (1999) J. Biol. Chem. 274, 22217-22224). Unexpectedly, we found that a global su amino acid substitution in tsf coat proteins made aggregation worse and that the tsf phenotype was suppressed by increasing the rate of subunit assembly, thereby decreasing the concentration of aggregation-prone folding intermediates.

Publication types

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

MeSH terms

  • Amino Acid Substitution
  • Bacteriophage P22 / chemistry
  • Bacteriophage P22 / genetics
  • Capsid / chemistry*
  • Capsid / genetics
  • Electrophoresis, Polyacrylamide Gel
  • Mutation
  • Phenotype
  • Protein Conformation*
  • Protein Folding*
  • Temperature
  • Tosyl Compounds
  • Viral Proteins / chemistry*
  • Viral Proteins / genetics
  • Viral Structural Proteins / chemistry
  • Viral Structural Proteins / genetics

Substances

  • Tosyl Compounds
  • Viral Proteins
  • Viral Structural Proteins
  • scaffolding protein, bacteriophage P22
  • arf protein, Enterobacteria phage P22
  • 4-toluenesulfonyl fluoride