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氟-19核磁共振化学位移与5-氟尿嘧啶取代的转运核糖核酸二级和三级结构之间的相关性

Correlations between fluorine-19 nuclear magnetic resonance chemical shift and the secondary and tertiary structure of 5-fluorouracil-substituted tRNA.

作者信息

Chu W C, Kintanar A, Horowitz J

机构信息

Department of Biochemistry and Biophysics, Iowa State University, Ames 50011.

出版信息

J Mol Biol. 1992 Oct 20;227(4):1173-81. doi: 10.1016/0022-2836(92)90529-s.

Abstract

To complete assignment of the 19F nuclear magnetic resonance (NMR) spectrum of 5-fluorouracil-substituted Escherichia coli tRNA(Val), resonances from 5-fluorouracil residues involved in tertiary interactions have been identified. Because these assignments could not be made directly by the base-replacement method used to assign 5-fluorouracil residues in loop and stem regions of the tRNA, alternative assignment strategies were employed. FU54 and FU55 were identified by 19F homonuclear Overhauser experiments and were then assigned by comparison of their 19F NMR spectra with those of 5-fluorouracil-labeled yeast tRNA(Phe) mutants having FU54 replaced by adenine and FU55 replaced by cytosine. FU8 and FU12, were assigned from the 19F NMR spectrum of the tRNA(Val) mutant in which the base triple G9-C23-G12 substituted for the wild-type A9-A23-FU12. Although replacement of the conserved U8 (FU8) with A or C disrupts the tertiary structure of tRNA(Val), it has only a small effect on the catalytic turnover number of valyl-tRNA synthetase, while reducing the affinity of the tRNA for enzyme. Analysis of the 19F chemical shift assignments of all 14 resonances in the spectrum of 5-fluorouracil-substituted tRNAVal indicated a strong correlation to tRNA secondary and tertiary structure. 5-Fluorouracil residues in loop regions gave rise to peaks in the central region of the spectrum, 4.4 to 4.9 parts per million (p.p.m.) downfield from free 5-fluorouracil. However, the signal from FU59, in the T-loop of tRNA(Val), was shifted more than 1 p.p.m. downfield, to 5.9 p.p.m., presumably because of the involvement of this fluorouracil in the tertiary interactions between the T and D-loops. The 19F chemical shift moved upfield, to the 2.0 to 2.8 p.p.m. range, when fluorouracil was base-paired with adenine in helical stems. This upfield shift was less pronounced for the fluorine of the FU7.A66 base-pair, located at the base of the acceptor stem, an indication that FU7 is only partially stacked on the adjacent G49 in the continuous acceptor stem/T-stem helix. An unanticipated finding was that the 19F resonances of 5-fluorouracil residues wobble base-paired with guanine were shifted 4 to 5 p.p.m. downfield of those from fluorouracil residues paired with A. In the 19F NMR spectra of all fluorinated tRNAs studied, the farthest downfield peak corresponded to FU55, which replaced the conserved pseudouridine normally found at this position.

摘要

为完成5-氟尿嘧啶取代的大肠杆菌tRNA(Val)的19F核磁共振(NMR)谱的归属,已鉴定出参与三级相互作用的5-氟尿嘧啶残基的共振信号。由于无法通过用于确定tRNA环和茎区域中5-氟尿嘧啶残基归属的碱基置换方法直接进行这些归属,因此采用了替代的归属策略。通过19F同核Overhauser实验鉴定出FU54和FU55,然后通过将它们的19F NMR谱与5-氟尿嘧啶标记的酵母tRNA(Phe)突变体的谱进行比较来进行归属,这些突变体中FU54被腺嘌呤取代,FU55被胞嘧啶取代。FU8和FU12是从tRNA(Val)突变体的19F NMR谱中归属的,该突变体中碱基三联体G9-C23-G12取代了野生型的A9-A23-FU12。尽管用A或C取代保守的U8(FU8)会破坏tRNA(Val)的三级结构,但它对缬氨酰-tRNA合成酶的催化周转数只有很小的影响,同时降低了tRNA对酶的亲和力。对5-氟尿嘧啶取代的tRNAVal谱中所有14个共振的19F化学位移归属分析表明,其与tRNA的二级和三级结构有很强的相关性。环区域中的5-氟尿嘧啶残基在谱的中心区域产生峰,相对于游离5-氟尿嘧啶,其场下位移为4.4至4.9百万分之一(ppm)。然而,tRNA(Val)的T环中的FU59的信号场下位移超过1 ppm,至5.9 ppm,推测是因为该氟尿嘧啶参与了T环和D环之间的三级相互作用。当氟尿嘧啶在螺旋茎中与腺嘌呤碱基配对时,19F化学位移向高场移动,至2.0至2.8 ppm范围。位于受体茎基部的FU7.A66碱基对的氟的这种高场位移不太明显,这表明FU7仅部分堆叠在连续的受体茎/T-茎螺旋中的相邻G49上。一个意外的发现是,与鸟嘌呤摆动碱基配对的5-氟尿嘧啶残基的19F共振相对于与A配对的氟尿嘧啶残基的共振向场下位移4至5 ppm。在所有研究的氟化tRNA的19F NMR谱中,最场下的峰对应于FU55,它取代了通常在该位置发现的保守假尿苷。

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