针对铜绿假单胞菌的 AEROPATH 项目:用于评估早期药物发现潜在目标的晶体学研究。

IF 0.9 4区 生物学
Lucille Moynie, Robert Schnell, Stephen A McMahon, Tatyana Sandalova, Wassila Abdelli Boulkerou, Jason W Schmidberger, Magnus Alphey, Cyprian Cukier, Fraser Duthie, Jolanta Kopec, Huanting Liu, Agata Jacewicz, William N Hunter, James H Naismith, Gunter Schneider
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引用次数: 0

摘要

由于抗生素耐药性的蔓延,细菌感染越来越难以治疗。革兰氏阴性细菌是一个主要问题,而新抗菌药物的发现尤其稀少。为了加快药物发现的早期步骤,欧盟资助的 AEROPATH 项目旨在通过多学科方法,包括靶点验证、结构表征、检测开发和从小分子库中识别新靶点,来确定机会性病原体铜绿假单胞菌的新靶点。本文介绍了选择靶点的策略,并报告了蛋白质生产和结构分析方面的进展。在 102 个选定的靶标中,84 个可以生产出可溶性形式,39 个蛋白质的全新结构已经确定。本文报告了其中 8 个靶标的晶体结构,这些靶标包括从假定未知蛋白到不同功能类别的代谢酶(PA1645、PA1648、PA2169、PA3770、PA4098、PA4485、PA4992 和 PA5259)。这些结构信息有望为改进从基于片段的高通量筛选活动中发现的命中化合物提供坚实的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The AEROPATH project targeting Pseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery.

The AEROPATH project targeting Pseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery.

The AEROPATH project targeting Pseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery.

The AEROPATH project targeting Pseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery.

Bacterial infections are increasingly difficult to treat owing to the spread of antibiotic resistance. A major concern is Gram-negative bacteria, for which the discovery of new antimicrobial drugs has been particularly scarce. In an effort to accelerate early steps in drug discovery, the EU-funded AEROPATH project aims to identify novel targets in the opportunistic pathogen Pseudomonas aeruginosa by applying a multidisciplinary approach encompassing target validation, structural characterization, assay development and hit identification from small-molecule libraries. Here, the strategies used for target selection are described and progress in protein production and structure analysis is reported. Of the 102 selected targets, 84 could be produced in soluble form and the de novo structures of 39 proteins have been determined. The crystal structures of eight of these targets, ranging from hypothetical unknown proteins to metabolic enzymes from different functional classes (PA1645, PA1648, PA2169, PA3770, PA4098, PA4485, PA4992 and PA5259), are reported here. The structural information is expected to provide a firm basis for the improvement of hit compounds identified from fragment-based and high-throughput screening campaigns.

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来源期刊
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审稿时长
2-4 weeks
期刊介绍: Acta Crystallographica Section F is a rapid structural biology communications journal. Articles on any aspect of structural biology, including structures determined using high-throughput methods or from iterative studies such as those used in the pharmaceutical industry, are welcomed by the journal. The journal offers the option of open access, and all communications benefit from unlimited free use of colour illustrations and no page charges. Authors are encouraged to submit multimedia content for publication with their articles. Acta Cryst. F has a dedicated online tool called publBio that is designed to make the preparation and submission of articles easier for authors.
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