Location bias: A “Hidden Variable” in GPCR pharmacology

Author:

Eiger Dylan Scott12ORCID,Hicks Chloe3ORCID,Gardner Julia3ORCID,Pham Uyen4ORCID,Rajagopal Sudarshan45ORCID

Affiliation:

1. Department of Medicine Brigham and Women's Hospital Boston Massachusetts USA

2. Harvard Medical School Boston Massachusetts USA

3. Trinity College Duke University Durham North Carolina USA

4. Department of Biochemistry Duke University Durham North Carolina USA

5. Department of Medicine Duke University Durham North Carolina USA

Abstract

AbstractG protein‐coupled receptors (GPCRs) are the largest family of transmembrane receptors and primarily signal through two main effector proteins: G proteins and β‐arrestins. Many agonists of GPCRs promote “biased” responses, in which different cellular signaling pathways are activated with varying efficacies. The mechanisms underlying biased signaling have not been fully elucidated, with many potential “hidden variables” that regulate this behavior. One contributor is “location bias,” which refers to the generation of unique signaling cascades from a given GPCR depending upon the cellular location at which the receptor is signaling. Here, we review evidence that GPCRs are expressed at and traffic to various subcellular locations and discuss how location bias can impact the pharmacologic properties and characterization of GPCR agonists. We also evaluate how differences in subcellular environments can modulate GPCR signaling, highlight the physiological significance of subcellular GPCR signaling, and discuss the therapeutic potential of exploiting GPCR location bias.

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

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