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FtsK 样马达 TraB 是一种依赖 DNA 的 ATP 酶,可形成更高阶的组装体。

The FtsK-like motor TraB is a DNA-dependent ATPase that forms higher-order assemblies.

机构信息

From the Departamento de Biología Molecular and Instituto de Biomedicina y Biotecnología de Cantabria (IBBTEC), Universidad de Cantabria-Consejo Superior de Investigaciones Científicas, Santander, Spain and.

Interfakultaeres Institut für Mikrobiologie und Infektionsmedizin Tuebingen IMIT, Mikrobiologie/Biotechnologie, Eberhard Karls Universitaet Tuebingen, 72074 Tuebingen, Germany.

出版信息

J Biol Chem. 2019 Mar 29;294(13):5050-5059. doi: 10.1074/jbc.RA119.007459. Epub 2019 Feb 5.

Abstract

TraB is an FtsK-like DNA translocase responsible for conjugative plasmid transfer in mycelial Unlike other conjugative systems, which depend on a type IV secretion system, requires only TraB protein to transfer the plasmid as dsDNA. The γ-domain of this protein specifically binds to repeated 8-bp motifs on the plasmid sequence, following a mechanism that is reminiscent of the FtsK/SpoIIIE chromosome segregation system. In this work, we purified and characterized the enzymatic activity of TraB, revealing that it is a DNA-dependent ATPase that is highly stimulated by dsDNA substrates. Interestingly, we found that unlike the SpoIIIE protein, the γ-domain of TraB does not confer sequence-specific ATPase stimulation. We also found that TraB binds G-quadruplex DNA structures with higher affinity than TraB-recognition sequences (TRSs). An EM-based structural analysis revealed that TraB tends to assemble as large complexes comprising four TraB hexamers, which might be a prerequisite for DNA translocation across cell membranes. In summary, our findings shed light on the molecular mechanism used by the DNA-translocating motor TraB, which may be shared by other membrane-associated machineries involved in DNA binding and translocation.

摘要

TraB 是一种类似于 FtsK 的 DNA 转位酶,负责菌丝体中可移动质粒的转移。与其他依赖 IV 型分泌系统的转导系统不同,该系统仅需要 TraB 蛋白即可将质粒作为 dsDNA 进行转移。该蛋白的γ结构域特异性结合质粒序列上的重复 8bp 基序,其机制类似于 FtsK/SpoIIIE 染色体分离系统。在这项工作中,我们纯化并表征了 TraB 的酶活性,揭示其是一种依赖 DNA 的 ATP 酶,dsDNA 底物对其具有高度的刺激作用。有趣的是,我们发现与 SpoIIIE 蛋白不同,TraB 的 γ结构域不能赋予序列特异性的 ATP 酶刺激。我们还发现 TraB 与 G-四链体 DNA 结构的结合亲和力高于 TraB 识别序列 (TRS)。基于 EM 的结构分析表明,TraB 倾向于组装成包含四个 TraB 六聚体的大复合物,这可能是跨细胞膜进行 DNA 转位的前提。总之,我们的研究结果阐明了 DNA 转位马达 TraB 所使用的分子机制,该机制可能被其他涉及 DNA 结合和转位的膜相关机制所共享。

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