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细菌释放因子的核糖体结构域。位于核糖体主体内的大肠杆菌核糖体蛋白L7/L12二聚体的羧基末端结构域对于释放因子相互作用很重要。

The ribosomal domain of the bacterial release factors. The carboxyl-terminal domain of the dimer of Escherichia coli ribosomal protein L7/L12 located in the body of the ribosome is important for release factor interaction.

作者信息

Tate W P, Kastner B, Edgar C D, McCaughan K K, Timms K M, Trotman C N, Stoffler-Meilicke M, Stoffler G, Nag B, Traut R R

机构信息

Department of Biochemistry, University of Otago, Dunedin, New Zealand.

出版信息

Eur J Biochem. 1990 Feb 14;187(3):543-8. doi: 10.1111/j.1432-1033.1990.tb15335.x.

Abstract
  1. Polyclonal antibodies (pAb 1-73 and pAb 26-120) have been raised against both an N-terminal fragment of Escherichia coli ribosomal protein L7/L12 (amino acids 1-73), and a fragment lacking part of the N-terminal domain (amino acids 26-120). 2. Only pAb 26-120 inhibited release-factor-dependent in vitro termination functions on the ribosome. This antibody binds over the length of the stalk of the large subunit of the ribosome as determined by immune electron microscopy, thereby not distinguishing between the C-terminal domains of the two L7/L12 dimers, those in the stalk or those in the body of the subunit. 3. A monoclonal antibody against an epitope of the C-terminal two thirds of the protein (mAb 74-120), which binds both to the distal tip of the stalk as well as to a region at its base, reflecting the positions of the two dimers is strongly inhibitory of release factor function. 4. A monoclonal antibody against an epitope of the N-terminal fragment of L7/L12 (mAb 1-73), previously shown to remove the dimer of L7/L12 in the 50S subunit stalk but still bind to the body of the particle, partially inhibited release-factor-mediated events. 5. The mAb 74-120 inhibited in vitro termination with a similar profile when the stalk dimer of L7/L12 was removed with mAb 1-73, indicating that the body L7/L12 dimer, and in particular its C-terminal domains, are important for release factor/ribosome interaction. 6. The two release factors have subtle differences in their binding domains with respect to L7/L12.
摘要
  1. 已制备出针对大肠杆菌核糖体蛋白L7/L12 N端片段(氨基酸1 - 73)和缺少部分N端结构域的片段(氨基酸26 - 120)的多克隆抗体(pAb 1 - 73和pAb 26 - 120)。2. 只有pAb 26 - 120能抑制核糖体上依赖释放因子的体外终止功能。免疫电子显微镜检测表明,该抗体结合在核糖体大亚基柄的全长上,因此无法区分两个L7/L12二聚体的C端结构域,无论是柄上的还是亚基主体中的。3. 一种针对该蛋白C端三分之二表位的单克隆抗体(mAb 74 - 120),它既结合柄的远端,也结合其基部区域,反映了两个二聚体的位置,对释放因子功能有强烈抑制作用。4. 一种针对L7/L12 N端片段表位的单克隆抗体(mAb 1 - 73),先前已证明它能去除50S亚基柄中的L7/L12二聚体,但仍能结合颗粒主体,它部分抑制了释放因子介导的事件。5. 当用mAb 1 - 73去除L7/L12的柄二聚体时,mAb 74 - 120以类似的方式抑制体外终止,这表明主体L7/L12二聚体,特别是其C端结构域,对释放因子/核糖体相互作用很重要。6. 两种释放因子在与L7/L12的结合结构域上存在细微差异。

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