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生物活性小分子的靶标去卷积:化学生物学和药物发现的核心。

Target deconvolution of bioactive small molecules: the heart of chemical biology and drug discovery.

机构信息

Department of BT-Convergent Pharmaceutical Engineering, Sun Moon University, 70, Sunmoon-ro 221, Tangjeong-myeon, Asan-si, Chungnam, 336-708, Republic of Korea.

Department of Biotechnology, Translational Research Center for Protein Function Control, College of Life Science and Biotechnology, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-749, Republic of Korea.

出版信息

Arch Pharm Res. 2015 Sep;38(9):1627-41. doi: 10.1007/s12272-015-0618-3. Epub 2015 Jun 4.

Abstract

Identification of the target proteins of bioactive small molecules isolated from phenotypic screens plays an important role in chemical biology and drug discovery. However, discovering the targets of small molecules is often the most challenging and time-consuming step for chemical biology researchers. To overcome the bottlenecks in target identification, many new approaches based on genomics, proteomics, and bioinformatics technologies have been developed. Here, we provide an overview of the current major methodologies for target deconvolution of bioactive small molecules. To obtain an integrated view of the mechanisms of action of small molecules, we propose a systematic approach that involves the combination of multi-omics-based target identification and validation and preclinical target validation.

摘要

从表型筛选中分离得到的生物活性小分子的靶蛋白的鉴定在化学生物学和药物发现中起着重要作用。然而,发现小分子的靶标通常是化学生物学研究人员最具挑战性和耗时的步骤。为了克服靶标鉴定中的瓶颈,已经开发了许多基于基因组学、蛋白质组学和生物信息学技术的新方法。在这里,我们提供了生物活性小分子靶标分解的当前主要方法的概述。为了获得小分子作用机制的综合视图,我们提出了一种系统的方法,包括基于多组学的靶标鉴定和验证以及临床前靶标验证的结合。

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