Dissecting receptor-G protein specificity using G alpha chimeras

Methods Enzymol. 2002:344:69-81. doi: 10.1016/s0076-6879(02)44706-4.

Abstract

In conclusion, by taking advantage of the overall sequence homology and structural similarity of G alpha subunits, functional chimeric G alpha subunits can be generated and used as tools for the identification of sequence-specific factors that mediate receptor: G protein specificity. The [35S]GTP gamma S binding assay and the affinity shift activity assay are two sensitive biochemical approaches that can be used to assess receptor: G protein coupling in vitro. These in vitro assays limit confounding influences from cellular proteins and allow for the strict control of receptor: G protein ratios.

MeSH terms

  • Animals
  • Cattle
  • Cell Line
  • Cell Membrane / metabolism
  • GTP-Binding Protein alpha Subunits, Gq-G11
  • Guanosine 5'-O-(3-Thiotriphosphate) / metabolism
  • Heterotrimeric GTP-Binding Proteins / isolation & purification
  • Heterotrimeric GTP-Binding Proteins / metabolism*
  • Kinetics
  • Protein Binding
  • Protein Subunits
  • Radioisotope Dilution Technique
  • Receptors, Cell Surface / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Proteins / metabolism
  • Rod Cell Outer Segment / metabolism
  • Sensitivity and Specificity
  • Spodoptera
  • Sulfur Radioisotopes
  • Transfection

Substances

  • Protein Subunits
  • Receptors, Cell Surface
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • Sulfur Radioisotopes
  • Guanosine 5'-O-(3-Thiotriphosphate)
  • GTP-Binding Protein alpha Subunits, Gq-G11
  • Heterotrimeric GTP-Binding Proteins