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探索药物研发中翻译后修饰的全貌。

Exploring the landscape of post-translational modification in drug discovery.

作者信息

Cao Yuhao, Yu Tianyi, Zhu Ziang, Zhang Yuanjiao, Sun Shanliang, Li Nianguang, Gu Chunyan, Yang Ye

机构信息

Nanjing Hospital of Chinese Medicine affiliated to Nanjing University of Chinese Medicine, Nanjing 210022, China; School of Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China.

School of Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China.

出版信息

Pharmacol Ther. 2025 Jan;265:108749. doi: 10.1016/j.pharmthera.2024.108749. Epub 2024 Nov 16.

Abstract

Post-translational modifications (PTMs) play a crucial role in regulating protein function, and their dysregulation is frequently associated with various diseases. The emergence of epigenetic drugs targeting factors such as histone deacetylases (HDACs) and histone methyltransferase enhancers of zeste homolog 2 (EZH2) has led to a significant shift towards precision medicine, offering new possibilities to overcome the limitations of traditional therapeutics. In this review, we aim to systematically explore how small molecules modulate PTMs. We discuss the direct targeting of enzymes involved in PTM pathways, the modulation of substrate proteins, and the disruption of protein-enzyme interactions that govern PTM processes. Additionally, we delve into the emerging strategy of employing multifunctional molecules to precisely regulate the modification levels of proteins of interest (POIs). Furthermore, we examine the specific characteristics of these molecules, evaluating their therapeutic benefits and potential drawbacks. The goal of this review is to provide a comprehensive understanding of PTM-targeting strategies and their potential for personalized medicine, offering a forward-looking perspective on the evolution of precision therapeutics.

摘要

翻译后修饰(PTMs)在调节蛋白质功能中起着至关重要的作用,其失调常常与各种疾病相关。靶向组蛋白脱乙酰酶(HDACs)和zeste同源物2(EZH2)等组蛋白甲基转移酶增强子等因子的表观遗传药物的出现,已导致向精准医学的重大转变,为克服传统疗法的局限性提供了新的可能性。在本综述中,我们旨在系统地探讨小分子如何调节翻译后修饰。我们讨论了直接靶向参与翻译后修饰途径的酶、调节底物蛋白以及破坏控制翻译后修饰过程的蛋白质-酶相互作用。此外,我们深入研究了采用多功能分子精确调节目标蛋白质(POIs)修饰水平的新兴策略。此外,我们研究了这些分子的具体特性,评估它们的治疗益处和潜在缺点。本综述的目的是全面了解靶向翻译后修饰的策略及其在个性化医学中的潜力,为精准治疗的发展提供前瞻性视角。

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