Structure and dynamics of Escherichia coli chemosensory receptors. Engineered sulfhydryl studies

Biophys J. 1992 Apr;62(1):209-16; discussion 217-9. doi: 10.1016/S0006-3495(92)81806-4.


Cysteine residues introduced by site-directed mutagenesis have been used to probe the conformation and dynamics of two receptors in the E. coli chemotaxis pathway. (a) Thermal motions of the polypeptide backbone were investigated in the periplasmic D-galactose and D-glucose receptor, a globular protein of known structure. Disulfide bond formation between pairs of engineered sulfhydryls were used to trap collisions during the relative motions of surface alpha-helices I and X. Motions with amplitudes ranging from 4.5 to 15.2 A were detected on timescales ranging from 10(-4) to 10(-1) s, respectively. These results suggest that thermal backbone motions may have larger amplitudes than previously thought. (b) Conformational features of the transmembrane aspartate transducer have been investigated. Engineered sulfhydryls were used to ascertain the location and orientations of two putative transmembrane alpha-helices in the primary structure, to investigate the packing of these helices, to determine the oligomer and surface structures, and to detect thermal and ligand-induced dynamics of the polypeptide backbone. A model for the folded conformation of the transducer oligomer is reviewed.

MeSH terms

  • Aspartic Acid / metabolism
  • Biophysical Phenomena
  • Biophysics
  • Cysteine / chemistry
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Galactose / metabolism
  • Glucose / metabolism
  • Molecular Structure
  • Mutagenesis, Site-Directed
  • Protein Conformation
  • Protein Engineering
  • Receptors, Amino Acid*
  • Receptors, Cell Surface / chemistry*
  • Receptors, Cell Surface / genetics


  • Receptors, Amino Acid
  • Receptors, Cell Surface
  • aspartic acid receptor
  • galactose receptor
  • glucose receptor
  • Aspartic Acid
  • Glucose
  • Cysteine
  • Galactose