Structure-based biophysical analysis of the interaction of rhodopsin with G protein and arrestin.

Abstract:

:In this chapter, we describe a set of complementary techniques that we use to study the activation of rhodopsin, a G protein-coupled receptor (GPCR), and its functional interactions with G protein and arrestin. The protein reagents used for these studies come from native disc membranes or heterologous expression, and G protein and arrestin are often replaced with less complex synthetic peptides derived from key interaction sites of these binding partners (BPs). We first report on our approach to protein X-ray crystallography and describe how protein crystals from native membranes are obtained. The crystal structures provide invaluable resolution, but other techniques are required to assess the dynamic equilibria characteristic for active GPCRs. The simplest approach is "Extra Meta II," which uses UV/Vis absorption spectroscopy to monitor the equilibrium of photoactivated states. Site-specific information about the BPs (e.g., arrestin) is added by fluorescence techniques employing mutants labeled with reporter groups. All functional changes in both the receptor and interacting proteins or peptides are seen with highest precision using Fourier transform infrared (FTIR) difference spectroscopy. In our approach, the lack of site-specific information in FTIR is overcome by parallel molecular dynamics simulations, which are employed to interpret the results and to extend the timescale down to the range of conformational substates.

journal_name

Methods Enzymol

journal_title

Methods in enzymology

authors

Sommer ME,Elgeti M,Hildebrand PW,Szczepek M,Hofmann KP,Scheerer P

doi

10.1016/bs.mie.2014.12.014

subject

Has Abstract

pub_date

2015-01-01 00:00:00

pages

563-608

eissn

0076-6879

issn

1557-7988

pii

S0076-6879(14)00128-1

journal_volume

556

pub_type

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