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15N标记的转运RNA。通过1H-15N二维核磁共振光谱法鉴定大肠杆菌丝氨酸转运RNA1和酪氨酸转运RNA2中的4-硫尿苷。

15N-labeled tRNA. Identification of 4-thiouridine in Escherichia coli tRNASer1 and tRNATyr2 by 1H-15N two-dimensional NMR spectroscopy.

作者信息

Griffey R H, Davis D R, Yamaizumi Z, Nishimura S, Hawkins B L, Poulter C D

出版信息

J Biol Chem. 1986 Sep 15;261(26):12074-8.

PMID:3638307
Abstract

Uridine is uniquely conserved at position 8 in elongator tRNAs and binds to A14 to form a reversed Hoogsteen base pair which folds the dihydrouridine loop back into the core of the L-shaped molecule. On the basis of 1H NMR studies, Hurd and co-workers (Hurd, R. E., Robillard, G. T., and Reid, B. R. (1977) Biochemistry 16, 2095-2100) concluded that the interaction between positions 8 and 14 is absent in Escherichia coli tRNAs with only 3 base pairs in the dihydrouridine stem. We have taken advantage of the unique 15N chemical shift of N3 in thiouridine to identify 1H and 15N resonances for the imino units of S4U8 and s4U9 in E. coli tRNASer1 and tRNATyr2. Model studies with chloroform-soluble derivatives of uridine and 4-thiouridine show that the chemical shifts of the protons in the imino moieties move downfield from 7.9 to 14.4 ppm and from 9.1 to 15.7 ppm, respectively; whereas, the corresponding 15N chemical shifts move downfield from 157.5 to 162.5 ppm and from 175.5 to 180.1 ppm upon hydrogen bonding to 5'-O-acetyl-2',3'-isopropylidene adenosine. The large difference in 15N chemical shifts for U and s4U allows one to unambiguously identify s4U imino resonances by 15N NMR spectroscopy. E. coli tRNASer1 and tRNATyr2 were selectively enriched with 15N at N3 of all uridines and modified uridines. Two-dimensional 1H-15N chemical shift correlation NMR spectroscopy revealed that both tRNAs have resonances with 1H and 15N chemical shifts characteristic of s4UA pairs. The 1H shift is approximately 1 ppm upfield from the typical s4U8 resonance at 14.8 ppm, presumably as a result of local diamagnetic anisotropies. An additional s4U resonance with 1H and 15N shifts typical of interaction of a bound water or a sugar hydroxyl group with s4U9 was discovered in the spectrum of tRNATyr2. Our NMR results for tRNAs with 3-base pair dihydrouridine stems suggest that these molecules have an U8A14 tertiary interaction similar to that found in tRNAs with 4-base pair dihydrouridine stems.

摘要

尿苷在延伸因子tRNA的第8位是独特保守的,它与A14结合形成反向Hoogsteen碱基对,从而将二氢尿嘧啶环折叠回L形分子的核心。基于1H NMR研究,赫德及其同事(赫德,R. E.,罗比拉德,G. T.,和里德,B. R.(1977年)《生物化学》16,2095 - 2100)得出结论,在二氢尿嘧啶茎中只有3个碱基对的大肠杆菌tRNA中不存在第8位和第14位之间的相互作用。我们利用硫代尿苷中N3独特的15N化学位移来识别大肠杆菌tRNASer1和tRNATyr2中S4U8和s4U9亚氨基单元的1H和15N共振。用尿苷和4 - 硫代尿苷的氯仿可溶性衍生物进行的模型研究表明,亚氨基部分质子的化学位移分别从7.9 ppm和9.1 ppm向低场移动到14.4 ppm和15.7 ppm;而当与5'-O - 乙酰基 - 2',3'-异亚丙基腺苷形成氢键时,相应的15N化学位移从157.5 ppm和175.5 ppm向低场移动到162.5 ppm和180.1 ppm。U和s4U的15N化学位移差异很大,这使得人们能够通过15N NMR光谱明确识别s4U亚氨基共振。大肠杆菌tRNASer1和tRNATyr2在所有尿苷和修饰尿苷的N3处选择性富集15N。二维1H - 15N化学位移相关NMR光谱显示,两种tRNA都有具有s4UA对特征的1H和15N化学位移的共振。1H位移比典型的14.8 ppm的s4U8共振高约1 ppm,这可能是由于局部抗磁各向异性。在tRNATyr2的光谱中发现了另一个具有与结合水或糖羟基与s4U9相互作用典型的1H和15N位移的s4U共振。我们对具有3个碱基对二氢尿嘧啶茎的tRNA的NMR结果表明,这些分子具有与具有4个碱基对二氢尿嘧啶茎的tRNA中发现的类似的U8A14三级相互作用。

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