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转运RNA在大肠杆菌核糖体中的转运。转运RNA 3'末端与23S核糖体RNA在A、P和E位点的特定核苷酸之间的交联。

Transit of tRNA through the Escherichia coli ribosome. Cross-linking of the 3' end of tRNA to specific nucleotides of the 23 S ribosomal RNA at the A, P, and E sites.

作者信息

Wower J, Kirillov S V, Wower I K, Guven S, Hixson S S, Zimmermann R A

机构信息

Department of Animal and Dairy Sciences, Program in Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849-5415, USA.

出版信息

J Biol Chem. 2000 Dec 1;275(48):37887-94. doi: 10.1074/jbc.M005031200.

Abstract

When bound to Escherichia coli ribosomes and irradiated with near-UV light, various derivatives of yeast tRNA(Phe) containing 2-azidoadenosine at the 3' terminus form cross-links to 23 S rRNA and 50 S subunit proteins in a site-dependent manner. A and P site-bound tRNAs, whose 3' termini reside in the peptidyl transferase center, label primarily nucleotides U2506 and U2585 and protein L27. In contrast, E site-bound tRNA labels nucleotide C2422 and protein L33. The cross-linking patterns confirm the topographical separation of the peptidyl transferase center from the E site domain. The relative amounts of label incorporated into the universally conserved residues U2506 and U2585 depend on the occupancy of the A and P sites by different tRNA ligands and indicates that these nucleotides play a pivotal role in peptide transfer. In particular, the 3'-adenosine of the peptidyl-tRNA analogue, AcPhe-tRNA(Phe), remains in close contact with U2506 regardless of whether its anticodon is located in the A site or P site. Our findings, therefore, modify and extend the hybrid state model of tRNA-ribosome interaction. We show that the 3'-end of the deacylated tRNA that is formed after transpeptidation does not immediately progress to the E site but remains temporarily in the peptidyl transferase center. In addition, we demonstrate that the E site, defined by the labeling of nucleotide C2422 and protein L33, represents an intermediate state of binding that precedes the entry of deacylated tRNA into the F (final) site from which it dissociates into the cytoplasm.

摘要

当与大肠杆菌核糖体结合并受到近紫外光照射时,3' 末端含有 2-叠氮腺苷的酵母苯丙氨酸转运核糖核酸(tRNA(Phe))的各种衍生物会以位点依赖的方式与 23 S 核糖体核糖核酸(rRNA)和 50 S 亚基蛋白形成交联。A 位点和 P 位点结合的 tRNA,其 3' 末端位于肽基转移酶中心,主要标记核苷酸 U2506 和 U2585 以及蛋白 L27。相比之下,E 位点结合的 tRNA 标记核苷酸 C2422 和蛋白 L33。交联模式证实了肽基转移酶中心与 E 位点结构域在拓扑学上是分离的。掺入普遍保守残基 U2506 和 U2585 的标记相对量取决于不同 tRNA 配体对 A 位点和 P 位点的占据情况,这表明这些核苷酸在肽转移中起关键作用。特别是,肽基 - tRNA 类似物 AcPhe - tRNA(Phe) 的 3'-腺苷无论其反密码子位于 A 位点还是 P 位点,都与 U2506 保持紧密接触。因此,我们的发现修正并扩展了 tRNA - 核糖体相互作用的杂交态模型。我们表明,转肽后形成的脱酰基 tRNA 的 3' 末端不会立即进入 E 位点,而是暂时留在肽基转移酶中心。此外,我们证明,由核苷酸 C2422 和蛋白 L33 的标记所定义的 E 位点代表了一种结合的中间状态,在脱酰基 tRNA 进入 F(最终)位点并从该位点解离进入细胞质之前。

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