Removing an interhelical salt bridge abolishes coiled-coil formation in a de novo designed peptide

J Struct Biol. 2002 Jan-Feb;137(1-2):65-72. doi: 10.1006/jsbi.2002.4467.

Abstract

Alpha-helical coiled coils represent a common protein oligomerization motif that are mainly stabilized by hydrophobic interactions occurring along their coiled-coil interface, the so-called hydrophobic seam. We have recently de novo designed and optimized a series of two-heptad repeat long coiled-coil peptides which are further stabilized by a complex network of inter- and intrahelical salt bridges. Here we have extended the de novo design of such two heptad-repeat long peptides by removing the central and most important g-e' Arg to Glu (g-e'RE) ionic interhelical interaction and replacing these residues by alanine residues. The effect of the missing interhelical ionic interaction on coiled-coil formation and stability has been analyzed by CD spectroscopy, analytical ultracentrifugation, and X-ray crystallography. We show that the peptide, while being highly alpha-helical, is no longer able to form a parallel coiled-coil structure but rather assumes an octameric globular helical assembly devoid of any coiled-coil interactions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Arginine / chemistry
  • Biophysics / methods*
  • Circular Dichroism
  • Crystallography, X-Ray
  • Glutamic Acid / chemistry
  • Ions
  • Models, Molecular
  • Molecular Sequence Data
  • Peptides / chemistry*
  • Protein Binding
  • Protein Folding
  • Protein Structure, Tertiary
  • Salts / chemistry*
  • Temperature
  • Ultracentrifugation

Substances

  • Ions
  • Peptides
  • Salts
  • Glutamic Acid
  • Arginine