Suppr超能文献

MinE的二聚化和拓扑特异性功能存在于一个结构自主的C末端结构域中。

The dimerization and topological specificity functions of MinE reside in a structurally autonomous C-terminal domain.

作者信息

King G F, Rowland S L, Pan B, Mackay J P, Mullen G P, Rothfield L I

机构信息

Department of Biochemistry, University of Sydney, NSW, Australia.

出版信息

Mol Microbiol. 1999 Feb;31(4):1161-9. doi: 10.1046/j.1365-2958.1999.01256.x.

Abstract

Correct placement of the division septum in Escherichia coli requires the co-ordinated action of three proteins, MinC, MinD and MinE. MinC and MinD interact to form a non-specific division inhibitor that blocks septation at all potential division sites. MinE is able to antagonize MinCD in a topologically sensitive manner, as it restricts MinCD activity to the unwanted division sites at the cell poles. Here, we show that the topological specificity function of MinE residues in a structurally autonomous, trypsin-resistant domain comprising residues 31-88. Nuclear magnetic resonance (NMR) and circular dichroic spectroscopy indicate that this domain includes both alpha and beta secondary structure, while analytical ultracentrifugation reveals that it also contains a region responsible for MinE homodimerization. While trypsin digestion indicates that the anti-MinCD domain of MinE (residues 1-22) does not form a tightly folded structural domain, NMR analysis of a peptide corresponding to MinE1-22 indicates that this region forms a nascent helix in which the peptide rapidly interconverts between disordered (random coil) and alpha-helical conformations. This suggests that the N-terminal region of MinE may be poised to adopt an alpha-helical conformation when it interacts with the target of its anti-MinCD activity, presumably MinD.

摘要

大肠杆菌中隔膜的正确定位需要三种蛋白质MinC、MinD和MinE的协同作用。MinC和MinD相互作用形成一种非特异性的分裂抑制剂,它会阻断所有潜在分裂位点的隔膜形成。MinE能够以拓扑敏感的方式拮抗MinCD,因为它将MinCD的活性限制在细胞两极不需要的分裂位点。在这里,我们表明MinE残基的拓扑特异性功能存在于一个结构自主、抗胰蛋白酶的结构域中,该结构域包含31-88位的残基。核磁共振(NMR)和圆二色光谱表明该结构域同时包含α和β二级结构,而分析超速离心显示它还包含一个负责MinE同二聚化的区域。虽然胰蛋白酶消化表明MinE的抗MinCD结构域(1-22位残基)不形成紧密折叠的结构域,但对对应于MinE1-22的肽段进行NMR分析表明,该区域形成一个新生螺旋,其中肽段在无序(随机卷曲)和α-螺旋构象之间快速相互转换。这表明MinE的N端区域在与它的抗MinCD活性的靶点(可能是MinD)相互作用时可能准备采取α-螺旋构象。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验