Stabilization of an alpha-helical conformation in an isolated hexapeptide inhibitor of calmodulin

Biopolymers. 2001 Dec;59(7):467-76. doi: 10.1002/1097-0282(200112)59:7<467::AID-BIP1052>3.0.CO;2-5.

Abstract

The conformational properties of two hexapeptides, Ac-LWRILW-NH(2) and its D-amino acid counterpart Ac-lwrilw-NH(2), identified as calmodulin inhibitors using mixture-based synthetic combinatorial library approaches, have been characterised by NMR and CD spectroscopy. The peptides fold into an alpha-helical conformation in aqueous solution. The observed short- and medium-range nuclear Overhauser effects were consistent with the formation of an alpha-helical structure and a reasonably well-defined set of structures was obtained by using restraints from the NMR data in simulated annealing calculations. Analysis of glycine-substitution analogues demonstrated that all the amino acids that make up the peptide sequence are important for the stabilization of the alpha-helical conformation. The results suggest that a well-defined set of interactions is indispensable to allow alpha-helix formation in this short hexapeptide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calmodulin / antagonists & inhibitors*
  • Calmodulin / metabolism
  • Circular Dichroism
  • Drug Stability
  • Hot Temperature
  • Magnetic Resonance Spectroscopy / methods
  • Models, Molecular
  • Monte Carlo Method
  • Peptides / chemical synthesis
  • Peptides / chemistry*
  • Protein Structure, Secondary
  • Ultracentrifugation

Substances

  • Calmodulin
  • Peptides