Two opposite effects of cofilin on the thermal unfolding of F-actin: a differential scanning calorimetric study

Biophys Chem. 2004 Jul 1;110(1-2):119-28. doi: 10.1016/j.bpc.2004.01.009.

Abstract

Differential scanning calorimetry was used to examine the effects of cofilin on the thermal unfolding of actin. Stoichiometric binding increases the thermal stability of both G- and F-actin but at sub-saturating concentrations cofilin destabilizes F-actin. At actin:cofilin molar ratios of 1.5-6 the peaks corresponding to stabilized (66-67 degrees C) and destabilized (56-57 degrees C) F-actin are observed simultaneously in the same thermogram. Destabilizing effects of sub-saturating cofilin are highly cooperative and are observed at actin:cofilin molar ratios as low as 100:1. These effects are abolished by the addition of phalloidin or aluminum fluoride. Conversely, at saturating concentrations, cofilin prevents the stabilizing effects of phalloidin and aluminum fluoride on the F-actin thermal unfolding. These results suggest that cofilin stabilizes those actin subunits to which it directly binds, but destabilizes F-actin with a high cooperativity in neighboring cofilin-free regions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Depolymerizing Factors
  • Actins / chemistry*
  • Aluminum Compounds / pharmacology
  • Calorimetry, Differential Scanning
  • Drug Stability
  • Fluorides / pharmacology
  • Microfilament Proteins / chemistry
  • Microfilament Proteins / pharmacology*
  • Phalloidine / pharmacology
  • Protein Denaturation / drug effects*
  • Protein Folding
  • Temperature
  • Thermography

Substances

  • Actin Depolymerizing Factors
  • Actins
  • Aluminum Compounds
  • Microfilament Proteins
  • Phalloidine
  • Fluorides
  • aluminum fluoride