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De-Nterm-ining GLP1R signaling bias

Abstract:
Biased agonism has emerged as a promising strategy for improving incretin therapeutics, yet the structural determinants of signaling bias remain incompletely understood. Building on their recent parathyroid hormone 1 receptor–β-arrestin structure, Zhao and colleagues identify extracellular loop 3 as a conformational switch controlling glucagon-like peptide-1 receptor transducer selectivity, enabling rational design of biased agonists.
Publication status:
In press
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.tips.2026.08.002

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Oxford Centre for Diabetes, Endocrinology and Metabolism
Oxford college:
Green Templeton College
Role:
Author
ORCID:
0000-0002-8641-8568


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Funder identifier:
https://ror.org/050rgn017
Grant:
AMS5971128
25/0006885
24/0006744
22/0006389
23/0006627
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Funder identifier:
https://ror.org/00vqxjy61
Grant:
1-PNF-2025-1623-S-B
More from this funder
Funder identifier:
https://ror.org/03x94j517
Grant:
APP23529
More from this funder
Funder identifier:
https://ror.org/001aqnf71
Grant:
EP/X026833/1


Publisher:
Cell Press
Journal:
Trends in Pharmacological Sciences More from this journal
Publication date:
2026-08-27
Acceptance date:
2026-08-05
DOI:
EISSN:
1873-3735
ISSN:
0165-6147


Language:
English
Keywords:
Pubs id:
2454342
Local pid:
pubs:2454342
Deposit date:
2026-09-02
ARK identifier:

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