Future Directions in GPCR Biased Signaling and Ligand Pharmacology.

Q1 Pharmacology, Toxicology and Pharmaceutics
Dannya Estau, Zijian Li
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引用次数: 0

Abstract

G protein-coupled receptor (GPCR) biased signaling has emerged as a transformative paradigm, reshaping both fundamental understanding of receptor biology and pharmacological intervention. Significant advances have been made in deciphering the mechanisms underlying biased signaling and in the development of ligands that selectively engage specific pathways. Here, we outline key future directions in GPCR biased signaling and ligand pharmacology including the biased signaling theories, structural insights, methodological innovations and ligand pharmacology theories. We hope that these perspectives will contribute to pharmacological research, drug R & D, and clinical drug research and promoting safer and more effective GPCR-targeted treatments for human diseases.

GPCR偏导信号和配体药理学的未来研究方向。
G蛋白偶联受体(GPCR)偏信号已经成为一种变革性的范式,重塑了对受体生物学和药物干预的基本理解。在解读偏倚信号传导的机制和选择性参与特定途径的配体的发展方面取得了重大进展。在这里,我们概述了GPCR偏导信号和配体药理学的关键未来方向,包括偏导信号理论、结构见解、方法创新和配体药理学理论。我们希望这些观点将有助于药理学研究、药物研发和临床药物研究,促进更安全、更有效的gpcr靶向治疗人类疾病。
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来源期刊
Handbook of experimental pharmacology
Handbook of experimental pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.20
自引率
0.00%
发文量
54
期刊介绍: The Handbook of Experimental Pharmacology is one of the most authoritative and influential book series in pharmacology. It provides critical and comprehensive discussions of the most significant areas of pharmacological research, written by leading international authorities. Each volume in the series represents the most informative and contemporary account of its subject available, making it an unrivalled reference source.
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