Conversion of two-state to multi-state folding kinetics on fusion of two protein foldons

J Mol Biol. 2000 Sep 8;302(1):219-33. doi: 10.1006/jmbi.2000.4024.

Abstract

Chymotrypsin inhibitor 2 (CI2) is the archetypal single-foldon protein that folds in simple two-state kinetics without the accumulation of a folding intermediate. To model the effects of fusion of single foldons to give a multi-foldon protein, we engineered a "double-CI2" protein, in which another CI2 polypeptide was inserted into the loop region of the parent CI2. CD and HSQC spectra demonstrated that while the double-CI2 protein adopted two kinds of native conformations, CI2-like structure was almost preserved in both the domains of double-CI2. In the folding kinetic studies, double-CI2 exhibited a remarkable rollover of the observed folding rates at low denaturant concentrations, indicating that double-CI2 accumulated a kinetic folding intermediate. The different folding mechanisms between WT-CI2 and double-CI2 support the present view that protein size or number of domains is an important determinant for formation of folding intermediates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Circular Dichroism
  • Guanidine / pharmacology
  • Hydrogen-Ion Concentration
  • Kinetics
  • Models, Molecular
  • Peptides / chemistry*
  • Peptides / metabolism
  • Plant Proteins
  • Protein Denaturation / drug effects
  • Protein Engineering*
  • Protein Folding*
  • Protein Renaturation
  • Protein Structure, Secondary / drug effects
  • Protein Structure, Tertiary / drug effects
  • Recombinant Fusion Proteins / chemistry*
  • Recombinant Fusion Proteins / metabolism
  • Thermodynamics
  • Ultraviolet Rays

Substances

  • Peptides
  • Plant Proteins
  • Recombinant Fusion Proteins
  • chymotrypsin inhibitor 2
  • Guanidine