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这些 TonB 二聚体晶体结构并不存在于体内。

The TonB dimeric crystal structures do not exist in vivo.

机构信息

Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania, USA.

出版信息

mBio. 2010 Dec 21;1(5):e00307-10. doi: 10.1128/mBio.00307-10.

Abstract

The TonB system energizes transport of nutrients across the outer membrane of Escherichia coli using cytoplasmic membrane proton motive force (PMF) for energy. Integral cytoplasmic membrane proteins ExbB and ExbD appear to harvest PMF and transduce it to TonB. The carboxy terminus of TonB then physically interacts with outer membrane transporters to allow translocation of ligands into the periplasmic space. The structure of the TonB carboxy terminus (residues ~150 to 239) has been solved several times with similar results. Our previous results hinted that in vitro structures might not mimic the dimeric conformations that characterize TonB in vivo. To test structural predictions and to identify irreplaceable residues, the entire carboxy terminus of TonB was scanned with Cys substitutions. TonB I232C and N233C, predicted to efficiently form disulfide-linked dimers in the crystal structures, did not do so. In contrast, Cys substitutions positioned at large distances from one another in the crystal structures efficiently formed dimers. Cys scanning identified seven functionally important residues. However, no single residue was irreplaceable. The phenotypes conferred by changes of the seven residues depended on both the specific assay used and the residue substituted. All seven residues were synergistic with one another. The buried nature of the residues in the structures was also inconsistent with these properties. Taken together, these results indicate that the solved dimeric crystal structures of TonB do not exist. The most likely explanation for the aberrant structures is that they were obtained in the absence of the TonB transmembrane domain, ExbB, ExbD, and/or the PMF.

摘要

TonB 系统利用细胞质膜质子动力势 (PMF) 为能量,为大肠杆菌的外膜运输营养物质提供能量。整合细胞质膜蛋白 ExbB 和 ExbD 似乎可以收获 PMF 并将其转导到 TonB。然后,TonB 的羧基末端与外膜转运蛋白物理相互作用,允许配体进入周质空间。TonB 羧基末端(残基~150 至 239)的结构已多次被解决,结果相似。我们之前的结果暗示,体外结构可能无法模拟 TonB 在体内的二聚体构象。为了测试结构预测并确定不可替代的残基,整个 TonB 羧基末端都进行了 Cys 取代扫描。TonB I232C 和 N233C,预计在晶体结构中能够有效地形成二硫键连接的二聚体,但实际上并未形成。相比之下,在晶体结构中彼此之间距离较大的 Cys 取代位置能够有效地形成二聚体。Cys 扫描确定了七个功能重要的残基。然而,没有一个单独的残基是不可替代的。七个残基的变化赋予的表型取决于所使用的特定测定方法和取代的残基。所有七个残基都具有协同作用。结构中残基的埋藏性质也与这些特性不一致。综上所述,这些结果表明,TonB 已解决的二聚体晶体结构并不存在。这些异常结构最可能的解释是,它们是在缺乏 TonB 跨膜结构域、ExbB、ExbD 和/或 PMF 的情况下获得的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a895/3005593/16039701b4b5/mbo0051010700001.jpg

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