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用于药物发现的细菌化合物积累测定法的进展和挑战。

Advances and challenges in bacterial compound accumulation assays for drug discovery.

机构信息

Infectious Diseases Area, Novartis Institutes for BioMedical Research, Emeryville, CA 94608, USA.

Infectious Diseases Area, Novartis Institutes for BioMedical Research, Emeryville, CA 94608, USA.

出版信息

Curr Opin Chem Biol. 2018 Jun;44:9-15. doi: 10.1016/j.cbpa.2018.05.005. Epub 2018 May 24.

Abstract

The identification of potent in vitro inhibitors of essential bacterial targets is relatively straightforward, however vanishingly few of these molecules have Gram-negative antibacterial potency and spectrum because of a failure to accumulate inside the bacteria. The Gram-negative bacterial cell envelope provides a formidable barrier to entry and couples with efflux pumps to prevent compound accumulation. Assays to measure the cellular permeation, efflux and accumulation of compounds in bacteria continue to be innovated and refined to guide drug discovery. Important advances in the label-free detection of compounds associated with or passing through bacteria rely on mass spectrometry This technique holds the promise of bacterial subcellular resolution and the throughput needed to test libraries of compounds to evaluate structure-accumulation relationships.

摘要

鉴定关键细菌靶标的有效体外抑制剂相对较为直接,然而,由于这些分子无法在细菌内部积累,因此极少数具有革兰氏阴性抗菌活性和广谱性。革兰氏阴性细菌的细胞包膜提供了一个强大的进入障碍,并与外排泵结合,以防止化合物的积累。用于测量化合物在细菌中的细胞渗透、外排和积累的测定方法在不断创新和完善,以指导药物发现。与细菌结合或通过细菌的化合物的无标记检测的重要进展依赖于质谱技术。该技术有望实现细菌亚细胞分辨率和高通量,从而可以测试化合物文库以评估结构-积累关系。

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