Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Advances in Yeast Synthetic Biology for Human GPCR Biology and Pharmacology

Published

Author(s)

Geoffrey Taghon, Nicholas Kapolka, Daniel Isom

Abstract

G protein-coupled receptors (GPCRs) are the largest family of transmembrane receptors in humans. Over 800 GPCRs regulate the (patho)biology of every organ, tissue, and cell type. Consequently, GPCRs are the most prominent therapeutic targets in medicine. Although over 30% of current FDA-approved drugs target GPCR signaling, most receptors remain understudied and therapeutically underutilized. Challenges include an incomplete understanding of GPCR signaling, pharmacology, structural biology, and the multiplicity of endogenous GPCR ligands, in addition to a scarcity of biological and pharmacological tools for elucidating GPCR-mediated cellular processes beyond initial signaling events. Various mammalian, insect, and yeast cell models currently address some of these needs. Here, we review recent advances in yeast synthetic biology that are helping to catalyze new and unexpected conceptual and technical breakthroughs in GPCR-based medicine and biotechnology.
Citation
Current Opinion in Biotechnology
Volume
88

Keywords

GPCRs, synthetic biology, yeast, biosensors, screening

Citation

Taghon, G. , Kapolka, N. and Isom, D. (2024), Advances in Yeast Synthetic Biology for Human GPCR Biology and Pharmacology, Current Opinion in Biotechnology, [online], https://doi.org/10.1016/j.copbio.2024.103176, https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=957792 (Accessed November 21, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created July 29, 2024, Updated August 5, 2024