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甲基转移酶样蛋白 16(METTL16):关键表观转录组学调控因子的探索之旅成为新兴的生物学靶点。

Methyl-Transferase-Like Protein 16 (METTL16): The Intriguing Journey of a Key Epitranscriptomic Player Becoming an Emerging Biological Target.

机构信息

Department of Pharmacy (DoE 2023-2027), University of Naples Federico II, via D. Montesano 49, 80131 Naples, Italy.

出版信息

J Med Chem. 2024 Sep 12;67(17):14786-14806. doi: 10.1021/acs.jmedchem.4c01247. Epub 2024 Aug 16.

Abstract

Key epitranscriptomic players have been increasingly characterized for their structural features and their involvement in several diseases. Accordingly, the design and synthesis of novel epitranscriptomic modulators have started opening a glimmer for drug discovery. m6A is a reversible modification occurring on a specific site and is catalyzed by three sets of proteins responsible for opposite functions. Writers (e.g., methyl-transferase-like protein (METTL) 3/METTL14 complex and METTL16) introduce the methyl group on adenosine -6, by transferring the methyl group from the methyl donor -adenosyl-methionine (SAM) to the substrate. Despite the rapidly advancing drug discovery progress on METTL3/METTL14, the METTL16 m6A writer has been marginally explored so far. We herein provide the first comprehensive overview of structural and biological features of METTL16, highlighting the state of the art in the field of its biological and structural characterization. We also showcase initial efforts in the identification of structural templates and preliminary structure-activity relationships for METTL16 modulators.

摘要

关键的表观转录组学调控因子的结构特征及其在多种疾病中的作用已逐渐被阐明。因此,新型表观转录组修饰剂的设计和合成开始为药物发现开辟了新的途径。m6A 是一种在特定位置发生的可逆修饰,由三组负责相反功能的蛋白质催化。writers(例如甲基转移酶样蛋白 (METTL) 3/METTL14 复合物和 METTL16)通过将甲基供体 S-腺苷甲硫氨酸 (SAM) 中的甲基转移到底物上来在腺苷-6 位引入甲基。尽管在 METTL3/METTL14 的药物发现方面取得了快速进展,但迄今为止,METTL16 的 m6A 书写器的研究仍处于起步阶段。本文提供了对 METTL16 的结构和生物学特征的全面概述,重点介绍了其生物学和结构特征研究领域的最新进展。我们还展示了鉴定 METTL16 调节剂的结构模板和初步结构-活性关系的初步努力。

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