Chemical Proteomics Reveals Human Off‐Targets of Fluoroquinolone Induced Mitochondrial Toxicity

Fluoroquinolones (FQs) are an important class of potent broad-spectrum antibiotics. However, their general use is more and more limited by adverse side effects. While general mechanisms for the fluoroquinolone-associated disability (FQAD) have been identified, the underlying molecular targets of toxicity remain elusive. In this study, focusing on the most commonly prescribed FQs Ciprofloxacin and Levofloxacin, whole proteome analyses revealed prominent mitochondrial dysfunction in human cells, specifically of the complexes I and IV of the electron transport chain (ETC). Furthermore, global untargeted chemo-proteomic methodologies such as photo-affinity profiling with FQ-derived probes, as well as derivatization-free thermal proteome profiling, were applied to elucidate human protein off-targets of FQs in living cells. Accordingly, the interactions of FQs with mitochondrial AIFM1 and IDH2 have been identified and biochemically validated for their contribution to mitochondrial dysfunction. Of note, the FQ induced ETC dysfunction via AIFM1 activates the reverse carboxylation pathway of IDH2 for rescue, however, its simultaneous inhibition further enhances mitochondrial toxicity. This off-target discovery study provides unique insights into FQ toxicity enabling the utilization of identified molecular principles for the design of a safer FQ generation.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-02-18
DOI
https://doi.org/10.1002/anie.202421424
Citations
10
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
8.06

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article

Chemical Proteomics Reveals Human Off‐Targets of Fluoroquinolone Induced Mitochondrial Toxicity

Jan Riemer, Robin Alexander Rothemann, Denitsa Docheva, Nina C. Bach et al.
10 citations
Angewandte Chemie International Edition
Advanced biosensing and bioanalysis techniques
8.06
article

Chemical Proteomics Reveals Human Off‐Targets of Fluoroquinolone Induced Mitochondrial Toxicity

Jan Riemer, Robin Alexander Rothemann, Denitsa Docheva, Nina C. Bach, Lianne H.C. Jacobs, Franziska R. Traube, Stephan A. Sieber, Yassmine El Harraoui, Martin F. Köllen, Sigrid Müller‐Deubert, Rolf Müller, Timo Risch, Till Reinhardt, A. Jauch, Stefan Zahler
article en
10 citations

Abstract

Fluoroquinolones (FQs) are an important class of potent broad-spectrum antibiotics. However, their general use is more and more limited by adverse side effects. While general mechanisms for the fluoroquinolone-associated disability (FQAD) have been identified, the underlying molecular targets of toxicity remain elusive. In this study, focusing on the most commonly prescribed FQs Ciprofloxacin and Levofloxacin, whole proteome analyses revealed prominent mitochondrial dysfunction in human cells, specifically of the complexes I and IV of the electron transport chain (ETC). Furthermore, global untargeted chemo-proteomic methodologies such as photo-affinity profiling with FQ-derived probes, as well as derivatization-free thermal proteome profiling, were applied to elucidate human protein off-targets of FQs in living cells. Accordingly, the interactions of FQs with mitochondrial AIFM1 and IDH2 have been identified and biochemically validated for their contribution to mitochondrial dysfunction. Of note, the FQ induced ETC dysfunction via AIFM1 activates the reverse carboxylation pathway of IDH2 for rescue, however, its simultaneous inhibition further enhances mitochondrial toxicity. This off-target discovery study provides unique insights into FQ toxicity enabling the utilization of identified molecular principles for the design of a safer FQ generation.

Angewandte Chemie International EditionVol. 64(18)
University of Stuttgart (DE), TH Köln - University of Applied Sciences (DE), University of Cologne (DE), University of Würzburg (DE), Klinik König-Ludwig Haus (DE), Helmholtz Centre for Infection Research (DE), Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (DE), Helmholtz Institute for Pharmaceutical Research Saarland (DE), Technical University of Munich (DE), Ludwig-Maximilians-Universität München (DE), Saarland University (DE)
European Commission, Bundesministerium für Bildung und Forschung
Openalex Percentile: Top 2%
Advanced biosensing and bioanalysis techniques
8.06
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