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http://hdl.handle.net/10872/8525
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Título : | Modelling antibiotic and cytotoxic isoquinoline effects inStaphylococcus aureus, Staphylococcus epidermidis and mammaliancells |
Autor : | Cecil, Alexander Ohlsen, Knut Menzel, Thomas Francois, Patrice Schrenzel, Jacques Fischer, Adrien Dörries, Kirsten Selle, Martina Lalk, Michael Hantzschmann, Julia Dittrich, Marcus Liang, Chunguang Bernhardt, Jörg Ölschläger, Tobias Bringmann, Gerhard Bruhn, Heike Unger, Matthias Ponte-Sucre, Alicia Lehmann, Leane Dandekar, Thomas |
Palabras clave : | metabolism infection pathway analysis gene expression |
Fecha de publicación : | 5-Mar-2015 |
Citación : | International Journal of Medical Microbiology;305:96-109, 2015 |
Resumen : | Isoquinolines (IQs) are natural substances with an antibiotic potential we aim to optimize. Specifically, IQ-238 is a synthetic analog of the novel-type N,C-coupled naphthylisoquinoline (NIQ) alkaloid ancisheynine.Recently, we developed and tested other IQs such as IQ-143. By utilizing genome-wide gene expressiondata, metabolic network modelling and Voronoi tessalation based data analysis – as well as cytotoxicitymeasurements, chemical properties calculations and principal component analysis of the NIQs – weshow that IQ-238 has strong antibiotic potential for staphylococci and low cytotoxicity against murine orhuman cells. Compared to IQ-143, systemic effects are less pronounced. Most enzyme activity changesdue to IQ-238 are located in the carbohydrate metabolism. Validation includes metabolite measurementson biological replicates. IQ-238 delineates key properties and a chemical space for a good therapeuticwindow. The combination of analysis methods allows suggestions for further lead development andyields an in-depth look at staphylococcal adaptation and network changes after antibiosis. Results arecompared to eukaryotic host cells. |
URI : | http://hdl.handle.net/10872/8525 |
ISSN : | 1438-4221 |
Aparece en las colecciones: | Artículos Publicados
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