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在DNA复制起始阶段,噬菌体λ复制起点处核蛋白结构的有序组装。

Ordered assembly of nucleoprotein structures at the bacteriophage lambda replication origin during the initiation of DNA replication.

作者信息

Alfano C, McMacken R

机构信息

Department of Biochemistry, School of Hygiene and Public Health, Johns Hopkins University, Baltimore, Maryland 21205.

出版信息

J Biol Chem. 1989 Jun 25;264(18):10699-708.

PMID:2525129
Abstract

Replication of the chromosome of bacteriophage lambda depends on the cooperative action of two phage-coded proteins and seven replication and heat shock proteins from its Escherichia coli host. As previously described, the first stage in this process is the binding of multiple copies of the lambda O initiator to the lambda replication origin (ori lambda) to form the nucleosomelike O-some. The O-some serves to localize subsequent protein-protein and protein-DNA interactions involved in the initiation of lambda DNA replication to ori lambda. To study these interactions, we have developed a sensitive immunoblotting protocol that permits the protein constituents of complex nucleoprotein structures to be identified. Using this approach, we have defined a series of sequential protein assembly and protein disassembly events that occur at ori lambda during the initiation of lambda DNA replication. A second-stage ori lambda.O (lambda O protein).P (lambda P protein).DnaB nucleoprotein structure is formed when O, P, and E. coli DnaB helicase are incubated with ori lambda DNA. In a third-stage reaction the E. coli DnaJ heat shock protein specifically binds to the second-stage structure to form an ori lambda.O.P.DnaB.DnaJ complex. Each of the nucleoprotein structures formed in the first three stages was isolated and shown to be a physiological intermediate in the initiation of lambda DNA replication. The E. coli DnaK heat shock protein can bind to any of these early stage nucleoprotein structures, and in a fourth-stage reaction a complete ori lambda.O.P.DnaB.DnaJ.DnaK initiation complex is assembled. Addition of ATP to the reaction enables the DnaK and DnaJ heat shock proteins to mediate a partial disassembly of the fourth-stage complex. These protein disassembly reactions activate the intrinsic helicase activity of DnaB and result in localized unwinding of the ori lambda template. The protein disassembly reactions are described in the accompanying articles.

摘要

噬菌体λ染色体的复制依赖于两种噬菌体编码蛋白以及来自其大肠杆菌宿主的七种复制和热休克蛋白的协同作用。如前所述,该过程的第一阶段是多个λO起始蛋白拷贝与λ复制起点(oriλ)结合,形成核小体样的O体。O体用于将参与λDNA复制起始的后续蛋白质 - 蛋白质和蛋白质 - DNA相互作用定位到oriλ。为了研究这些相互作用,我们开发了一种灵敏的免疫印迹方法,该方法能够鉴定复杂核蛋白结构的蛋白质成分。使用这种方法,我们确定了一系列在λDNA复制起始过程中发生在oriλ处的连续蛋白质组装和蛋白质拆卸事件。当O、P和大肠杆菌DnaB解旋酶与oriλDNA一起孵育时,形成第二阶段的oriλ.O(λO蛋白).P(λP蛋白).DnaB核蛋白结构。在第三阶段反应中,大肠杆菌DnaJ热休克蛋白特异性结合到第二阶段结构上,形成oriλ.O.P.DnaB.DnaJ复合物。在前三个阶段形成的每个核蛋白结构都被分离出来,并被证明是λDNA复制起始过程中的生理中间体。大肠杆菌DnaK热休克蛋白可以结合这些早期核蛋白结构中的任何一种,并且在第四阶段反应中组装成完整的oriλ.O.P.DnaB.DnaJ.DnaK起始复合物。向反应中添加ATP可使DnaK和DnaJ热休克蛋白介导第四阶段复合物的部分拆卸。这些蛋白质拆卸反应激活了DnaB的内在解旋酶活性,并导致oriλ模板的局部解旋。蛋白质拆卸反应在随附的文章中进行了描述。

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