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比较蛋白质组学反应作为阐明抗生素作用机制的整体方法。

Comparison of Proteomic Responses as Global Approach to Antibiotic Mechanism of Action Elucidation.

机构信息

Applied Microbiology, Faculty of Biology and Biotechnology, Ruhr University Bochum, Bochum, Germany.

Biochemistry and Molecular Biology, Pennsylvania State University, State College, Pennsylvania, USA.

出版信息

Antimicrob Agents Chemother. 2020 Dec 16;65(1). doi: 10.1128/AAC.01373-20.

Abstract

New antibiotics are urgently needed to address the mounting resistance challenge. In early drug discovery, one of the bottlenecks is the elucidation of targets and mechanisms. To accelerate antibiotic research, we provide a proteomic approach for the rapid classification of compounds into those with precedented and unprecedented modes of action. We established a proteomic response library of covering 91 antibiotics and comparator compounds, and a mathematical approach was developed to aid data analysis. Comparison of proteomic responses (CoPR) allows the rapid identification of antibiotics with dual mechanisms of action as shown for atypical tetracyclines. It also aids in generating hypotheses on mechanisms of action as presented for salvarsan (arsphenamine) and the antirheumatic agent auranofin, which is under consideration for repurposing. Proteomic profiling also provides insights into the impact of antibiotics on bacterial physiology through analysis of marker proteins indicative of the impairment of cellular processes and structures. As demonstrated for -translation, a promising target not yet exploited clinically, proteomic profiling supports chemical biology approaches to investigating bacterial physiology.

摘要

新抗生素的研发迫在眉睫,以应对日益严重的耐药性挑战。在早期药物发现中,一个瓶颈是阐明靶点和作用机制。为了加速抗生素研究,我们提供了一种蛋白质组学方法,可快速将化合物分为具有先例和前所未有的作用模式的化合物。我们建立了一个涵盖 91 种抗生素和对照化合物的蛋白质组反应文库,并开发了一种数学方法来辅助数据分析。蛋白质组反应比较(CoPR)可快速识别具有双重作用机制的抗生素,如非典型四环素类抗生素。它还有助于提出作用机制的假设,如对胂凡钠明(砷凡纳明)和抗风湿药金诺芬的作用机制的假设,金诺芬正在考虑重新利用。蛋白质组分析还通过分析指示细胞过程和结构受损的标记蛋白,深入了解抗生素对细菌生理学的影响。如翻译过程所示,这是一个尚未在临床上得到利用的有前途的靶点,蛋白质组分析支持化学生物学方法来研究细菌生理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d60e/7927858/b34adf0afdbc/AAC.01373-20-f0001.jpg

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