[Carbon 13 nuclear magnetic resonance conformation studies of peptides with analgesic activity]

Can J Biochem. 1980 Nov;58(11):1241-6.
[Article in French]

Abstract

13C Nuclear magnetic resonance studies of proline peptides with central antalgic activity (Pro-Arg, Arg-Pro, Pro-Arg-Pro, Pro-Lys-Pro) indicate a predominance of trans conformation at all pH values; but their physiological activities appear to be related to the ability of the C-terminal proline peptides to assume the cis conformation.

Publication types

  • English Abstract

MeSH terms

  • Analgesics / analysis*
  • Magnetic Resonance Spectroscopy
  • Oligopeptides / analysis*
  • Proline / analysis*
  • Protein Conformation

Substances

  • Analgesics
  • Oligopeptides
  • Proline