Stereoelectronic effects on collagen stability: the dichotomy of 4-fluoroproline diastereomers

J Am Chem Soc. 2003 Aug 6;125(31):9262-3. doi: 10.1021/ja035881z.

Abstract

Collagen is the most abundant protein in animals. Natural collagen consists of a triple helix of (Xaa-Yaa-Gly)n chains, in which the Xaa and Yaa residues are often l-proline. Here, a (2S,4S)-4-fluoroproline (flp) residue is shown to be greatly stabilizing in the Xaa position (but destabilizing in the Yaa position). In contrast, a (2S,4R)-4-fluoroproline (Flp) residue is shown to be greatly destabilizing in the Xaa position (but stabilizing in the Yaa position). The dichotomous effect of the diastereomers appears to arise from a gauche effect, which alters pyrrolidine ring pucker and hence properly (or improperly) preorganizes main-chain dihedral angles. Thus, the rational use of stereoelectronic effects can enhance the conformational stability of a protein.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Circular Dichroism
  • Collagen / chemistry*
  • Hydroxyproline / chemistry
  • Proline / analogs & derivatives
  • Proline / chemistry*
  • Protein Folding
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • fluoro-proline
  • Collagen
  • Proline
  • Hydroxyproline