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有证据表明,一种细菌三联多药泵以 3:6:3 的化学计量比组装。

Evidence for the assembly of a bacterial tripartite multidrug pump with a stoichiometry of 3:6:3.

机构信息

School of Biological and Biomedical Sciences, Durham University, South Road, Durham DH1 3LE, United Kingdom.

出版信息

J Biol Chem. 2011 Jul 29;286(30):26900-12. doi: 10.1074/jbc.M111.246595. Epub 2011 May 24.

Abstract

The multiple transferable resistance (mTR) pump from Neisseria gonorrhoeae MtrCDE multidrug pump is assembled from the inner and outer membrane proteins MtrD and MtrE and the periplasmic membrane fusion protein MtrC. Previously we established that while there is a weak interaction of MtrD and MtrE, MtrC binds with relatively high affinity to both MtrD and MtrE. MtrD conferred antibiotic resistance only when it was expressed with MtrE and MtrC, suggesting that these proteins form a functional tripartite complex in which MtrC bridges MtrD and MtrE. Furthermore, we demonstrated that MtrC interacts with an intraprotomer groove on the surface of MtrE, inducing channel opening. However, a second groove is apparent at the interface of the MtrE subunits, which might also be capable of engaging MtrC. We have now established that MtrC can be cross-linked to cysteines placed in this interprotomer groove and that mutation of residues in the groove impair the ability of the pump to confer antibiotic resistance by locking MtrE in the closed channel conformation. Moreover, MtrE K390C forms an intermolecular disulfide bond with MtrC E149C locking MtrE in the open channel conformation, suggesting that a functional salt bridge forms between these residues during the transition from closed to open channel conformations. MtrC forms dimers that assemble into hexamers, and electron microscopy studies of single particles revealed that these hexamers are arranged into ring-like structures with an internal aperture sufficiently large to accommodate the MtrE trimer. Cross-linking of single cysteine mutants of MtrC to stabilize the dimer interface in the presence of MtrE, trapped an MtrC-MtrE complex with a molecular mass consistent with a stoichiometry of 3:6 (MtrE(3)MtrC(6)), suggesting that dimers of MtrC interact with MtrE, presumably by binding to the two grooves. As both MtrE and MtrD are trimeric, our studies suggest that the functional pump is assembled with a stoichiometry of 3:6:3.

摘要

淋病奈瑟菌 MtrCDE 多药泵的多重转移耐药 (mTR) 泵由内膜蛋白 MtrD 和 MtrE 以及周质膜融合蛋白 MtrC 组成。以前我们已经确定,虽然 MtrD 和 MtrE 之间存在弱相互作用,但 MtrC 与 MtrD 和 MtrE 结合具有相对较高的亲和力。只有当 MtrD 与 MtrE 和 MtrC 表达时,MtrD 才赋予抗生素耐药性,这表明这些蛋白形成了一个功能性的三联复合物,其中 MtrC 桥接 MtrD 和 MtrE。此外,我们证明 MtrC 与 MtrE 表面的一个单体内部沟槽相互作用,诱导通道打开。然而,在 MtrE 亚基的界面上显然存在第二个沟槽,它也可能与 MtrC 结合。我们现在已经确定,MtrC 可以与放置在这个单体内部沟槽中的半胱氨酸交联,并且沟槽中的残基突变会通过将 MtrE 锁定在关闭的通道构象中来损害泵赋予抗生素耐药性的能力。此外,MtrE K390C 与 MtrC E149C 形成分子间二硫键,将 MtrE 锁定在开放通道构象中,这表明在从关闭到开放通道构象的转变过程中,这些残基之间形成了一个功能性盐桥。MtrC 形成二聚体,然后组装成六聚体,单颗粒电子显微镜研究表明,这些六聚体排列成具有足够大的内部孔径的环形结构,以容纳 MtrE 三聚体。在存在 MtrE 的情况下,交联 MtrC 的单个半胱氨酸突变体以稳定二聚体界面,捕获了一种分子量与 3:6 (MtrE(3)MtrC(6)) 摩尔比一致的 MtrC-MtrE 复合物,这表明 MtrC 的二聚体与 MtrE 相互作用,可能通过与两个沟槽结合。由于 MtrE 和 MtrD 都是三聚体,我们的研究表明,功能性泵的组装摩尔比为 3:6:3。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6f5/3143649/7dc9713ee9b3/zbc0341171110001.jpg

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