» Articles » PMID: 35606532

Yeast-based Directed-evolution for High-throughput Structural Stabilization of G Protein-coupled Receptors (GPCRs)

Overview
Journal Sci Rep
Specialty Science
Date 2022 May 23
PMID 35606532
Authors
Affiliations
Soon will be listed here.
Abstract

The immense potential of G protein-coupled receptors (GPCRs) as targets for drug discovery is not fully realized due to the enormous difficulties associated with structure elucidation of these profoundly unstable membrane proteins. The existing methods of GPCR stability-engineering are cumbersome and low-throughput; in addition, the scope of GPCRs that could benefit from these techniques is limited. Here, we present a yeast-based screening platform for a single-step isolation of GRCR variants stable in the presence of short-chain detergents, a feature essential for their successful crystallization using vapor diffusion method. The yeast detergent-resistant cell wall presents a unique opportunity for compartmentalization, to physically link the receptor's phenotype to its encoding DNA, and thus enable discovery of stable GPCR variants with unprecedent efficiency. The scope of mutations identified by the method reveals a surprising amenability of the GPCR scaffold to stabilization, and suggests an intriguing possibility of amending the stability properties of GPCR by varying the structural status of the C-terminus.

Citing Articles

Development of a yeast-based sensor platform for evaluation of ligands recognized by the human free fatty acid 2 receptor.

Clausen Lind A, De Castro Gomes D, Alcaraz R, Bisquert R, Martensson J, Sundqvist M FEMS Yeast Res. 2025; 25.

PMID: 39824656 PMC: 11781196. DOI: 10.1093/femsyr/foaf001.

References
1.
Scott D, Pluckthun A . Direct molecular evolution of detergent-stable G protein-coupled receptors using polymer encapsulated cells. J Mol Biol. 2012; 425(3):662-77. DOI: 10.1016/j.jmb.2012.11.015. View

2.
Ramprakash J, Doseeva V, Galkin A, Krajewski W, Muthukumar L, Pullalarevu S . Comparison of the chemical and thermal denaturation of proteins by a two-state transition model. Anal Biochem. 2007; 374(1):221-30. DOI: 10.1016/j.ab.2007.10.005. View

3.
Serrano-Vega M, Magnani F, Shibata Y, Tate C . Conformational thermostabilization of the beta1-adrenergic receptor in a detergent-resistant form. Proc Natl Acad Sci U S A. 2008; 105(3):877-82. PMC: 2242685. DOI: 10.1073/pnas.0711253105. View

4.
Vernall A, Hill S, Kellam B . The evolving small-molecule fluorescent-conjugate toolbox for Class A GPCRs. Br J Pharmacol. 2013; 171(5):1073-84. PMC: 3952789. DOI: 10.1111/bph.12265. View

5.
Fonin A, Darling A, Kuznetsova I, Turoverov K, Uversky V . Multi-functionality of proteins involved in GPCR and G protein signaling: making sense of structure-function continuum with intrinsic disorder-based proteoforms. Cell Mol Life Sci. 2019; 76(22):4461-4492. PMC: 11105632. DOI: 10.1007/s00018-019-03276-1. View