全基因组泛 GPCR 细胞文库加速药物发现

IF 14.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY
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引用次数: 0

摘要

G 蛋白偶联受体(GPCR)在介导各种生理和病理过程中起着关键作用,因此是药物发现的理想靶点。GPCR 约占美国 FDA 批准药物的 40%,是最成功的药物靶点。然而,在 800 种人类 GPCR 中,只有约 15% 的受体是市场药物的靶点,这就为剩余受体的药物发现留下了大量机会。细胞表达系统在 GPCR 药物发现领域发挥着至关重要的作用,包括新靶点识别、结构和功能表征、潜在配体筛选、信号通路阐明和药物安全性评估。在此,我们讨论了在 GPCR 靶向药物发现、GPCR 功能研究、信号通路表征和药理特性研究中广泛使用的细胞表达系统的原理、应用和局限性。我们还提出了构建全基因组泛 GPCR 细胞文库的三种策略,这将为 GPCR 配体筛选提供一个强大的平台,并促进 GPCR 机制研究和药物安全性评价,最终加速 GPCR 靶向药物发现的进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genome-wide pan-GPCR cell libraries accelerate drug discovery

Genome-wide pan-GPCR cell libraries accelerate drug discovery

Genome-wide pan-GPCR cell libraries accelerate drug discovery
G protein-coupled receptors (GPCRs) are pivotal in mediating diverse physiological and pathological processes, rendering them promising targets for drug discovery. GPCRs account for about 40% of FDA-approved drugs, representing the most successful drug targets. However, only approximately 15% of the 800 human GPCRs are targeted by market drugs, leaving numerous opportunities for drug discovery among the remaining receptors. Cell expression systems play crucial roles in the GPCR drug discovery field, including novel target identification, structural and functional characterization, potential ligand screening, signal pathway elucidation, and drug safety evaluation. Here, we discuss the principles, applications, and limitations of widely used cell expression systems in GPCR-targeted drug discovery, GPCR function investigation, signal pathway characterization, and pharmacological property studies. We also propose three strategies for constructing genome-wide pan-GPCR cell libraries, which will provide a powerful platform for GPCR ligand screening, and facilitate the study of GPCR mechanisms and drug safety evaluation, ultimately accelerating the process of GPCR-targeted drug discovery.
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来源期刊
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
22.40
自引率
5.50%
发文量
1051
审稿时长
19 weeks
期刊介绍: The Journal of the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association oversees the peer review process for Acta Pharmaceutica Sinica. B (APSB). Published monthly in English, APSB is dedicated to disseminating significant original research articles, rapid communications, and high-quality reviews that highlight recent advances across various pharmaceutical sciences domains. These encompass pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis, and pharmacokinetics. A part of the Acta Pharmaceutica Sinica series, established in 1953 and indexed in prominent databases like Chemical Abstracts, Index Medicus, SciFinder Scholar, Biological Abstracts, International Pharmaceutical Abstracts, Cambridge Scientific Abstracts, and Current Bibliography on Science and Technology, APSB is sponsored by the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association. Its production and hosting are facilitated by Elsevier B.V. This collaborative effort ensures APSB's commitment to delivering valuable contributions to the pharmaceutical sciences community.
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