Investigation on temperature-induce conformational change of immobilized β2 adrenergic receptor

Biochem Biophys Res Commun. 2017 Dec 16;494(3-4):634-640. doi: 10.1016/j.bbrc.2017.08.105. Epub 2017 Aug 26.

Abstract

The β2 adrenergic receptor (β2-AR) is a prototypical family A G protein-coupled receptor (GPCR) and an excellent model system for studying the mechanism of GPCR activation. Purified β2-AR was immobilized on macroporous silica gel to obtain liquid chromatographic stationary phase. The resulting phase was packed into a stainless steel column (4.6 × 50 mm, 7 μm) and used for on-line chromatographic system. When column oven temperature increased from 20.0 °C to 40.0 °C, uncomplete separate chromatographic peaks of ephedrine and pseudoephedrine as receptor conformational probe were gradually merged into one peak, meanwhile retention time and resolution of the probes were reduced correspondingly, which suggested that temperature could regulate protein conformation. Temperature-induced conformational change of immobilized β2-AR, especially changes at higher temperatures, indicated that constructed receptor chromatography could simulate fever disease state of human body and clarify receptor conformation change at pathological condition. At the same time this study could also provide new ideas for screening active components in pathological conditions.

Keywords: Ephedrine and pseudoephedrine; Protein conformation; Receptor chromatography; Temperature-induced; β(2) adrenergic receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Ephedrine / chemistry*
  • Protein Binding
  • Protein Conformation*
  • Protein Denaturation*
  • Receptors, Adrenergic, beta-2 / chemistry*
  • Receptors, Adrenergic, beta-2 / ultrastructure*
  • Temperature*

Substances

  • Receptors, Adrenergic, beta-2
  • Ephedrine