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首页> 外文期刊>Biochemistry >Identification of 50S components neighboring 23S rRNA nucleotides A2448 and U2604 within the peptidyl transferase center of Escherichia coli ribosomes.
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Identification of 50S components neighboring 23S rRNA nucleotides A2448 and U2604 within the peptidyl transferase center of Escherichia coli ribosomes.

机译:鉴定大肠杆菌核糖体肽基转移酶中心内23S rRNA核苷酸A2448和U2604附近的50S成分。

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摘要

The 23S rRNA nucleotides 2604-12 and 2448-58 fall within the central loop of domain V, which forms a major part of the peptidyl transferase center of the ribosome. We report the synthesis of radioactive, photolabile 2'-O-methyloligoRNAs, PHONTs 1 and 2, complementary to these nucleotides and their exploitation in identifying 50S ribosomal subunit components neighboring their target sites. Photolysis of the 50S complex with PHONT 1, complementary to nts 2604-12, leads to target site-specific photoincorporation into protein L2 and 23S rRNA nucleotides A886, Alpha1918, A1919, G1922-C1924, U2563, U2586, and C2601. Photolysis of the 50S complex with PHONT 2, complementary to nts 2448-58, leads to target site-specific probe photoincorporation into proteins L2, L3, one or more of proteins L17, L18, L21, and of proteins L9, L15, L16, and 23S rRNA nucleotides C2456 and psi2457. Chemical footprinting studies show that 2'-O-methyloligoRNA binding causes little distortion of the peptidyl transferase center but do provide suggestive evidence for the location of flexible regions within 23S rRNA. The significance of these results for the structure of the peptidyl transferase center is considered.
机译:23S rRNA核苷酸2604-12和2448-58属于结构域V的中央环,该环形成核糖体肽基转移酶中心的主要部分。我们报告了放射性,光不稳定的2'-O-methyloligoRNAs,PHONT 1和2,与这些核苷酸互补,并在确定与其靶点相邻的50S核糖体亚基组分中的利用,进行了合成。 50S复合物与PHONT 1的光解,与nts 2604-12互补,导致靶位点特异性光掺入蛋白L2和23S rRNA核苷酸A886,Alpha1918,A1919,G1922-C1924,U2563,U2586和C2601。 50S配合物与PHONT 2的光解与nts 2448-58互补,导致目标位点特异性探针光掺入蛋白质L2,L3,蛋白质L17,L18,L21和蛋白质L9,L15,L16中的一种或多种,和23S rRNA核苷酸C2456和psi2457。化学足迹研究表明2'-O-methyloligoRNA结合几乎不会引起肽基转移酶中心的扭曲,但确实为23S rRNA内的柔性区域定位提供了提示性证据。考虑了这些结果对于肽基转移酶中心的结构的重要性。

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