Assembly and inhibition of transferable TMexCD1-TOprJ1 efflux pump

Recent emergence and dissemination of plasmid-borne tmexCD1-toprJ1 tigecycline resistance threatens the efficacy of tigecycline as a "last-resort" defense against bacterial infections. Here, we report two cryo-EM structures of TMexCD1-TOprJ1 alone and in complex with its NMP inhibitor, and both are determined at the resolutions of 2.97 Å and 3.0 Å, respectively. The symmetry of overall architecture explains how the tripartite organization adopts a 3:6:3 protomer stoichiometry (TOprJ1: TMexC1: TMexD1) to assemble an elongated, rod-like pump spanning bacterial double membranes. The periplasmic TMexC1 adaptor bind the trimeric TOprJ1 funnel via a universal "tip-to-tip" contact, and bridges the bottom TMexD1 engine by extensive interactions. A unique form of resting (R) states is observed for TMexD1 trimer. Besides two binding-interfaces of TMexC1 with TOprJ1 and TMexD1, we characterize a substrate/inhibitor-loading cavity. Collectively, these findings constitute molecular bases for assembly and inhibition of transferable TMexCD1-TOprJ1 machinery, and benefit developing next-generation of antimicrobials targeting functional efflux pump.

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Publication Details

Journal
Nature Communications
Published
2025-11-14
DOI
https://doi.org/10.1038/s41467-025-65038-x
Citations
3
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
1.77
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article

Assembly and inhibition of transferable TMexCD1-TOprJ1 efflux pump

Yu Feng, Jianhua Gan, Mengyuan Li, Youjun Feng et al.
3 citations
Nature Communications
Antibiotic Resistance in Bacteria
1.77
article

Assembly and inhibition of transferable TMexCD1-TOprJ1 efflux pump

Yu Feng, Jianhua Gan, Mengyuan Li, Youjun Feng, Huimin Zhang, Xing Zhang, Yu Shi, Haomin Huang, Tao Cui, Su Zhi, Runshi Yang
article en
3 citations

Abstract

Recent emergence and dissemination of plasmid-borne tmexCD1-toprJ1 tigecycline resistance threatens the efficacy of tigecycline as a "last-resort" defense against bacterial infections. Here, we report two cryo-EM structures of TMexCD1-TOprJ1 alone and in complex with its NMP inhibitor, and both are determined at the resolutions of 2.97 Å and 3.0 Å, respectively. The symmetry of overall architecture explains how the tripartite organization adopts a 3:6:3 protomer stoichiometry (TOprJ1: TMexC1: TMexD1) to assemble an elongated, rod-like pump spanning bacterial double membranes. The periplasmic TMexC1 adaptor bind the trimeric TOprJ1 funnel via a universal "tip-to-tip" contact, and bridges the bottom TMexD1 engine by extensive interactions. A unique form of resting (R) states is observed for TMexD1 trimer. Besides two binding-interfaces of TMexC1 with TOprJ1 and TMexD1, we characterize a substrate/inhibitor-loading cavity. Collectively, these findings constitute molecular bases for assembly and inhibition of transferable TMexCD1-TOprJ1 machinery, and benefit developing next-generation of antimicrobials targeting functional efflux pump.

Nature CommunicationsVol. 16(1)
South China Agricultural University (CN), Ministry of Education (NZ), University of Illinois Urbana-Champaign (US), Northwestern Polytechnical University (CN), Fudan University (CN), Second Affiliated Hospital of Zhejiang University (CN), Zhejiang University (CN)
Openalex Percentile: Top 14%
Antibiotic Resistance in Bacteria
1.77
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