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肽基转移酶抗生素会干扰核糖体中P/P'位点结合的tRNA的3'末端腺苷与23S rRNA的相对位置。

Peptidyl transferase antibiotics perturb the relative positioning of the 3'-terminal adenosine of P/P'-site-bound tRNA and 23S rRNA in the ribosome.

作者信息

Kirillov S V, Porse B T, Garrett R A

机构信息

RNA Regulation Centre, Institute of Molecular Biology, University of Copenhagen, Denmark.

出版信息

RNA. 1999 Aug;5(8):1003-13. doi: 10.1017/s1355838299990568.

Abstract

A range of antibiotic inhibitors that act within the peptidyl transferase center of the ribosome were examined for their capacity to perturb the relative positioning of the 3' end of P/P'-site-bound tRNA and the Escherichia coli ribosome. The 3'-terminal adenosines of deacylated tRNA and N-Ac-Phe-tRNA were derivatized at the 2 position with an azido group and the tRNAs were cross-linked to the ribosome on irradiation with ultraviolet light at 365 nm. The cross-links were localized on the rRNA within extended versions of three previously characterized 23S rRNA fragments F1', F2', and F4' at nucleotides C2601/A2602, U2584/U2585 (F1'), U2506 (F2'), and A2062/C2063 (F4'). Each of these nucleotides lies within the peptidyl transferase loop region of the 23S rRNA. Cross-links were also formed with ribosomal proteins L27 (strong) and L33 (weak), as shown earlier. The antibiotics sparsomycin, chloramphenicol, the streptogramins pristinamycin IA and IIA, gougerotin, lincomycin, and spiramycin were tested for their capacity to alter the identities or yields of each of the cross-links. Although no new cross-links were detected, each of the drugs produced major changes in cross-linking yields, mainly decreases, at one or more rRNA sites but, with the exception of chloramphenicol, did not affect cross-linking to the ribosomal proteins. Moreover, the effects were closely similar for both deacylated and N-Ac-Phe-tRNAs, indicating that the drugs selectively perturb the 3' terminus of the tRNA. The strongest decreases in the rRNA cross-links were observed with pristinamycin IIA and chloramphenicol, which correlates with their both producing complex chemical footprints on 23S rRNA within E. coli ribosomes. Furthermore, gougerotin and pristinamycin IA strongly increased the yields of fragments F2' (U2506) and F4' (U2062/C2063), respectively. The results obtained with an RNAse H approach correlate well with primer extension data implying that cross-linking occurs primarily to the bases. Both sets of data are also consistent with the results of earlier rRNA footprinting experiments on antibiotic-ribosome complexes. It is concluded that the antibiotics perturb the relative positioning of the 3' end of the P/P'-site-bound tRNA and the peptidyl transferase loop region of 23S rRNA.

摘要

研究了一系列作用于核糖体肽基转移酶中心的抗生素抑制剂,以考察它们扰乱P/P'-位点结合的tRNA 3'端与大肠杆菌核糖体相对位置的能力。将去酰化tRNA和N-乙酰苯丙氨酰-tRNA的3'-末端腺苷在2位用叠氮基进行衍生化,然后在365nm紫外光照射下将tRNA与核糖体交联。交联位点定位在三个先前鉴定的23S rRNA片段F1'、F2'和F4'的延伸版本的rRNA上,分别位于核苷酸C2601/A2602、U2584/U2585(F1')、U2506(F2')和A2062/C2063(F4')处。这些核苷酸均位于23S rRNA的肽基转移酶环区域内。如先前所示,还与核糖体蛋白L27(强)和L33(弱)形成了交联。测试了抗生素稀疏霉素、氯霉素、链阳菌素IA和IIA、谷氏菌素、林可霉素和螺旋霉素改变每种交联的特性或产量的能力。虽然未检测到新的交联,但每种药物在一个或多个rRNA位点上均使交联产量发生了重大变化,主要是降低,但氯霉素除外,它不影响与核糖体蛋白的交联。此外,去酰化tRNA和N-乙酰苯丙氨酰-tRNA的效应非常相似,表明这些药物选择性地扰乱了tRNA的3'末端。在链阳菌素IIA和氯霉素作用下,观察到rRNA交联的下降最为明显,这与它们在大肠杆菌核糖体的23S rRNA上均产生复杂的化学足迹相关。此外,谷氏菌素和链阳菌素IA分别强烈增加了片段F2'(U2506)和F4'(U2062/C2063)的产量。用RNA酶H方法获得的结果与引物延伸数据高度相关,这意味着交联主要发生在碱基上。这两组数据也与早期关于抗生素-核糖体复合物的rRNA足迹实验结果一致。得出的结论是,这些抗生素扰乱了P/P'-位点结合的tRNA 3'端与23S rRNA肽基转移酶环区域的相对位置。

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