Structure-based engineering of environmentally sensitive fluorophores for monitoring protein-protein interactions.

Journal Article (Journal Article)

Single, extrinsic, environmentally sensitive fluorophores can be used to quantitate formation of protein-protein complexes. These can be prepared semi-synthetically by covalent coupling to single cysteine mutations introduced at positions where the fluorophore is predicted to respond to formation of the complex without adversely affecting the interaction. The three-dimensional structure of a protein-protein interface can be used to select such locations by identifying residues that are located at the edge of a buried interfacial region, and are in partial steric contact with both partners as indicated by a change in their static solvent-accessible surface area upon complex formation. Using this design approach, cysteine mutations were introduced into the B1 domain of protein G, which successfully monitor complex formation with minimal interference. Such constructs have great utility in the analysis of solution properties of interface mutants.

Full Text

Duke Authors

Cited Authors

  • Sloan, DJ; Hellinga, HW

Published Date

  • September 1998

Published In

Volume / Issue

  • 11 / 9

Start / End Page

  • 819 - 823

PubMed ID

  • 9796832

International Standard Serial Number (ISSN)

  • 0269-2139

Digital Object Identifier (DOI)

  • 10.1093/protein/11.9.819


  • eng

Conference Location

  • England