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A New Tool to Reveal Bacterial Signaling Mechanisms in Antibiotic Treatment and Resistance.


ABSTRACT: The rapid emergence of antimicrobial resistance is a major threat to human health. Antibiotics modulate a wide range of biological processes in bacteria and as such, the study of bacterial cellular signaling could aid the development of urgently needed new antibiotic agents. Due to the advances in bacterial phosphoproteomics, such a systemwide analysis of bacterial signaling in response to antibiotics has recently become feasible. Here we present a dynamic view of differential protein phosphorylation upon antibiotic treatment and antibiotic resistance. Most strikingly, differential phosphorylation was observed on highly conserved residues of resistance regulating transcription factors, implying a previously unanticipated role of phosphorylation mediated regulation. Using the comprehensive phosphoproteomics data presented here as a resource, future research can now focus on deciphering the precise signaling mechanisms contributing to resistance, eventually leading to alternative strategies to combat antimicrobial resistance.

SUBMITTER: Lin MH 

PROVIDER: S-EPMC6283303 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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A New Tool to Reveal Bacterial Signaling Mechanisms in Antibiotic Treatment and Resistance.

Lin Miao-Hsia MH   Potel Clement M CM   Tehrani Kamaleddin H M E KHME   Heck Albert J R AJR   Martin Nathaniel I NI   Lemeer Simone S  

Molecular & cellular proteomics : MCP 20180919 12


The rapid emergence of antimicrobial resistance is a major threat to human health. Antibiotics modulate a wide range of biological processes in bacteria and as such, the study of bacterial cellular signaling could aid the development of urgently needed new antibiotic agents. Due to the advances in bacterial phosphoproteomics, such a systemwide analysis of bacterial signaling in response to antibiotics has recently become feasible. Here we present a dynamic view of differential protein phosphoryl  ...[more]

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