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接合性质粒RP4的TraK蛋白与转移起始点形成一种特殊的核蛋白复合物。

TraK protein of conjugative plasmid RP4 forms a specialized nucleoprotein complex with the transfer origin.

作者信息

Ziegelin G, Pansegrau W, Lurz R, Lanka E

机构信息

Max-Planck-Institut für Molekulare Genetik, Abteilung Schuster, Berlin, Federal Republic of Germany.

出版信息

J Biol Chem. 1992 Aug 25;267(24):17279-86.

PMID:1324929
Abstract

Conjugative transfer of the self-transmissible IncP plasmid RP4 requires the product of the RP4 traK gene. By using the phage T7 expression system, the traK gene product was efficiently overproduced and purified to near homogeneity. traK encodes a basic protein (pI = 10.7) of 14.6 kDa that, as shown by DNA fragment retention assay, interacts exclusively with its cognate transfer origin. The apparent equilibrium constant K(app) for the complex of TraK and oriT-DNA was estimated to be 4 nM. Footprinting experiments using DNase I or hydroxyl radicals indicate that several TraK molecules interact specifically with an intrinsically bent region of oriT, covering a range of almost 200 base pairs. The TraK target sequence maps in the leading region adjacent to the relaxation nick site and recognition sequences involved in relaxosome formation but does not overlap them. Specific interactions between TraK and the DNA occur only on one side of the double helix. Electron microscopy of TraK-oriT complexes demonstrates that binding of TraK to its recognition region apparently shrinks the length of the target DNA, suggesting that the nucleic acid becomes wrapped around a core of TraK molecules. Formation of this structure could be favored by the presence of the sequence-directed bend in the TraK recognition region.

摘要

自我传递性IncP质粒RP4的接合转移需要RP4 traK基因的产物。通过使用噬菌体T7表达系统,traK基因产物得以高效过量表达并纯化至近乎均一的状态。traK编码一种14.6 kDa的碱性蛋白(pI = 10.7),如DNA片段保留试验所示,该蛋白仅与其同源转移起始位点相互作用。TraK与oriT - DNA复合物的表观平衡常数K(app)估计为4 nM。使用DNase I或羟基自由基进行的足迹实验表明,几个TraK分子与oriT的一个固有弯曲区域特异性相互作用,覆盖范围近200个碱基对。TraK靶序列定位于与松弛切口位点相邻的前导区域以及参与松弛体形成的识别序列,但不与之重叠。TraK与DNA之间的特异性相互作用仅发生在双螺旋的一侧。TraK - oriT复合物的电子显微镜观察表明,TraK与其识别区域的结合明显缩短了靶DNA的长度,这表明核酸围绕TraK分子核心缠绕。TraK识别区域中序列导向弯曲的存在可能有利于这种结构的形成。

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