Purification and characterization of the recombinant human dopamine D2S receptor from Pichia pastoris

Protein Expr Purif. 2004 Feb;33(2):176-84. doi: 10.1016/j.pep.2003.08.018.

Abstract

The human dopamine D2S receptor was expressed in the methylotrophic yeast Pichia pastoris, where the receptor with a molecular mass of approximately 40kDa exhibited specific and saturable binding properties. The dopamine antagonist [3H]spiperone showed an average dissociation constant K(d) of 0.6+/-0.17 nM for the dopamine D2S receptor. The receptor was solubilized using the non-ionic detergent dodecylmaltoside and purified by affinity chromatography using a Ni(2+) chelate (His-Trap) column or by batch extraction with an anti-FLAG M1 affinity resin. The receptor maintained its biological activity after solubilization and purification from the membrane protein fraction. A 244- or 185-fold enrichment, as judged by an increase in specific binding, was obtained after adsorption to the His-Trap or anti-FLAG materials, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Membrane / metabolism
  • Cholic Acids / chemistry
  • Culture Media
  • Humans
  • Molecular Weight
  • Pichia / genetics*
  • Pichia / metabolism
  • Protein Binding
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D2 / isolation & purification*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / isolation & purification
  • Sensitivity and Specificity
  • Solubility

Substances

  • Cholic Acids
  • Culture Media
  • Receptors, Dopamine D2
  • Recombinant Fusion Proteins
  • dopamine D2L receptor
  • 3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate