| Literature DB >> 33046497 |
Christoph H R Senges1, Jennifer J Stepanek1, Michaela Wenzel1, Nadja Raatschen1, Ümran Ay1, Yvonne Märtens1, Pascal Prochnow1, Melissa Vázquez Hernández1, Abdulkadir Yayci1, Britta Schubert1, Niklas B M Janzing1, Helen L Warmuth1, Martin Kozik1, Jens Bongard1, John N Alumasa2, Bauke Albada3, Maya Penkova3, Tadeja Lukežič4, Nohemy A Sorto5, Nicole Lorenz3, Reece G Miller3, Bingyao Zhu6, Martin Benda6, Jörg Stülke6, Sina Schäkermann1, Lars I Leichert7, Kathi Scheinpflug8, Heike Brötz-Oesterhelt9, Christian Hertweck10, Jared T Shaw5, Hrvoje Petković11, Jean M Brunel12, Kenneth C Keiler2, Nils Metzler-Nolte3, Julia E Bandow13.
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 Bacillus subtilis 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 trans-translation, a promising target not yet exploited clinically, proteomic profiling supports chemical biology approaches to investigating bacterial physiology.Entities:
Keywords: antibiotic; chemical biology; mechanism of action; physiology; proteomics
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Year: 2020 PMID: 33046497 PMCID: PMC7927858 DOI: 10.1128/AAC.01373-20
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191