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程序性细胞死亡蛋白1/程序性细胞死亡配体1通路抑制剂的研究进展及结合模式分析

Progress in programmed cell death-1/programmed cell death-ligand 1 pathway inhibitors and binding mode analysis.

作者信息

Li Xiaoyun, Zeng Qin, Xu Fengjiao, Jiang Yuying, Jiang Zhongmei

机构信息

Department of Pharmacy, Chun'an County Hospital of Traditional Chinese Medicine, Hangzhou, 311700, Zhejiang, China.

Laboratory of Pharmacology, Department of Pharmacology, School of Pharmacy, Sichuan University, Chengdu, 610041, Sichuan, China.

出版信息

Mol Divers. 2023 Aug;27(4):1935-1955. doi: 10.1007/s11030-022-10509-2. Epub 2022 Aug 10.

Abstract

Programmed cell death protein 1 (PD-1)/programmed cell death protein ligand 1 (PD-L1) plays an important role in negative regulating immunity. The search for effective PD-1/PD-L1 inhibitors has been at the cutting-edge of academic and industrial medicinal chemistry, leading to the emergence of 16 clinical candidate drugs and the launch of six monoclonal antibodies (mAbs) drugs. However, due to the unclear mechanism of the interaction between drugs and substances in vivo, the screening of preclinical drugs often takes a long time. In order to shorten the time of drug development as much as possible, the binding mode analysis that can simulate the interaction between drugs and substances in vivo at the molecular level can significantly shorten the drug development process. This paper reviews the mechanism of PD-1/PD-L1 signaling pathway at the molecular level, as well as the research progress and obstacles of inhibitors. Besides, we analyzed the binding mode of recently reported PD-1/PD-L1 inhibitors with PD-1 or PD-L1 protein in detail in order to provide ideas for the development of PD-1/PD-L1 inhibitors.

摘要

程序性细胞死亡蛋白1(PD-1)/程序性细胞死亡蛋白配体1(PD-L1)在免疫负调控中发挥重要作用。寻找有效的PD-1/PD-L1抑制剂一直是学术和工业药物化学的前沿领域,已催生了16种临床候选药物,并上市了6种单克隆抗体(mAb)药物。然而,由于药物与体内物质相互作用的机制尚不清楚,临床前药物的筛选往往耗时较长。为了尽可能缩短药物研发时间,能够在分子水平模拟药物与体内物质相互作用的结合模式分析可显著缩短药物研发过程。本文综述了PD-1/PD-L1信号通路在分子水平的机制,以及抑制剂的研究进展和障碍。此外,我们详细分析了最近报道的PD-1/PD-L1抑制剂与PD-1或PD-L1蛋白的结合模式,以便为PD-1/PD-L1抑制剂的开发提供思路。

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