+検索条件
-Structure paper
タイトル | Antibiotic export by MexB multidrug efflux transporter is allosterically controlled by a MexA-OprM chaperone-like complex. |
---|---|
ジャーナル・号・ページ | Nat Commun, Vol. 11, Issue 1, Page 4948, Year 2020 |
掲載日 | 2020年10月2日 |
著者 | Marie Glavier / Dhenesh Puvanendran / Dimitri Salvador / Marion Decossas / Gilles Phan / Cyril Garnier / Elisa Frezza / Quentin Cece / Guy Schoehn / Martin Picard / Jean-Christophe Taveau / Laetitia Daury / Isabelle Broutin / Olivier Lambert / |
PubMed 要旨 | The tripartite multidrug efflux system MexAB-OprM is a major actor in Pseudomonas aeruginosa antibiotic resistance by exporting a large variety of antimicrobial compounds. Crystal structures of MexB ...The tripartite multidrug efflux system MexAB-OprM is a major actor in Pseudomonas aeruginosa antibiotic resistance by exporting a large variety of antimicrobial compounds. Crystal structures of MexB and of its Escherichia coli homolog AcrB had revealed asymmetric trimers depicting a directional drug pathway by a conformational interconversion (from Loose and Tight binding pockets to Open gate (LTO) for drug exit). It remains unclear how MexB acquires its LTO form. Here by performing functional and cryo-EM structural investigations of MexB at various stages of the assembly process, we unveil that MexB inserted in lipid membrane is not set for active transport because it displays an inactive LTC form with a Closed exit gate. In the tripartite complex, OprM and MexA form a corset-like platform that converts MexB into the active form. Our findings shed new light on the resistance nodulation cell division (RND) cognate partners which act as allosteric factors eliciting the functional drug extrusion. |
リンク | Nat Commun / PubMed:33009415 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.2 - 4.5 Å |
構造データ | EMDB-10371: CryoEM structure of MexB in nanodisc EMDB-10372: CryoEM structure of MexAB-OprM in nanodisc EMDB-10395: MexA-MexB cryoEM map |
由来 |
|
キーワード | ANTIMICROBIAL PROTEIN / transporter / efflux / proton motive force / bacterial resistance |