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
{"title":"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。","authors":"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","doi":"10.1107/S1744309112044739","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":7310,"journal":{"name":"Acta Crystallographica Section F-structural Biology and Crystallization Communications","volume":"69 Pt 1","pages":"25-34"},"PeriodicalIF":0.9000,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539698/pdf/","citationCount":"0","resultStr":"{\"title\":\"The AEROPATH project targeting Pseudomonas aeruginosa: crystallographic studies for assessment of potential targets in early-stage drug discovery.\",\"authors\":\"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\",\"doi\":\"10.1107/S1744309112044739\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bacterial infections are increasingly difficult to treat owing to the spread of antibiotic resistance. 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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.
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.