G Protein-Coupled Receptor Dimerization—What Next?

Author:

Dziedzicka-Wasylewska Marta1,Polit Agnieszka2ORCID,Błasiak Ewa2,Faron-Górecka Agata1ORCID

Affiliation:

1. Department of Pharmacology, Maj Institute of Pharmacology, Polish Academy of Science, Smętna Street 12, 31-343 Kraków, Poland

2. Department of Physical Biochemistry, Faculty of Biochemistry Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland

Abstract

Numerous studies highlight the therapeutic potential of G protein-coupled receptor (GPCR) heterodimers, emphasizing their significance in various pathological contexts. Despite extensive basic research and promising outcomes in animal models, the translation of GPCR heterodimer-targeting drugs into clinical use remains limited. The complexities of in vivo conditions, particularly within thecomplex central nervous system, pose challenges in fully replicating physiological environments, hindering clinical success. This review discusses examples of the most studied heterodimers, their involvement in nervous system pathology, and the available data on their potential ligands. In addition, this review highlights the intricate interplay between lipids and GPCRs as a potential key factor in understanding the complexity of cell signaling. The multifaceted role of lipids in modulating the dynamics of GPCR dimerization is explored, shedding light on the elaborate molecular mechanisms governing these interactions.

Funder

statutory funds of the Maj Institute of Pharmacology of the Polish Academy of Sciences

statutory funds of the Faculty of Biochemistry, Biophysics and Biotechnology of the Jagiellonian University

Publisher

MDPI AG

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. GPR41 and GPR43: From development to metabolic regulation;Biomedicine & Pharmacotherapy;2024-06

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