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在一个对称的14碱基对乳糖假操纵基因DNA片段中磷-31和非交换质子共振的归属

Assignment of phosphorus-31 and nonexchangeable proton resonances in a symmetrical 14 base pair lac pseudooperator DNA fragment.

作者信息

Schroeder S A, Fu J M, Jones C R, Gorenstein D G

机构信息

Department of Chemistry, Purdue University, West Lafayette, Indiana 47907.

出版信息

Biochemistry. 1987 Jun 30;26(13):3812-21. doi: 10.1021/bi00387a012.

Abstract

The 31P chemical shifts of all 13 phosphates and the chemical shifts of nearly all of the non-exchangeable protons of a symmetrical 14 base pair lac pseudooperator DNA fragment have been assigned by regiospecific labeling with oxygen-17 and two-dimensional NMR techniques. At 22 degrees C, 8 of the 13 phosphorus resonances can distinctly be resolved while the remaining 5 resonances occur in two separate overlapping regions. The 31P chemical shifts of this particular 14 base pair oligonucleotide do not follow the general observation that the more internal the phosphate is located within the oligonucleotide sequence the more upfield the 31P resonance occurs, as shown from other 31P assignment studies. Failure of this general rule is believed to be a result of helical distortions that occur along the oligonucleotide double helix, on the basis of the analysis of Callidine [Callidine, C.R. (1982) J. Mol. Biol. 161, 343-352]. Notable exceptions to the phosphate position relationship are 5'-Py-Pu-3' dinucleotide sequences, which resonate at a lower field strength than expected in agreement with similar results as reported by Ott and Eckstein [Ott, J., & Eckstein, F. (1985) Biochemistry 24, 253]. A reasonable correlation exists between 31P chemical shifts values of the 14-mer and the helical twist sum function of Calladine. The most unusual 31P resonance occurs most upfield in the 31P spectrum, which has been assigned to the second phosphate position (5'-GpT-3') from the 5' end. This unusual chemical shift may be the result of the predicted large helical twist angle that occurs at this position in the 14-mer sequence. Further, it is believed that the large helical twist represents a unique structural feature responsible for optimum binding contact between lac repressor protein and this 14-mer lac pseudooperator segment. Assignments of proton resonances were made from two-dimensional 1H-1H nuclear Overhauser effect (NOESY) connectivities in a sequential manner applicable to right-handed B-DNA, in conjunction with two-dimensional homonuclear and heteronuclear J-correlated spectroscopies (1H-1H COSY and 31P-1H HETCOR). Most nonexchangeable base proton and deoxyribose proton (except for some unresolved H4', H5', and H5" protons) resonances were assigned.

摘要

通过用氧 - 17进行区域特异性标记和二维核磁共振技术,已对一个对称的14碱基对乳糖假操纵基因DNA片段中所有13个磷酸基团的³¹P化学位移以及几乎所有非交换质子的化学位移进行了归属。在22摄氏度时,13个磷共振峰中有8个能够清晰分辨,而其余5个共振峰出现在两个单独的重叠区域。与其他³¹P归属研究结果不同,这个特定的14碱基对寡核苷酸的³¹P化学位移并不遵循一般规律,即磷酸基团在寡核苷酸序列中位置越靠内,³¹P共振峰越靠上场。根据卡利丁的分析[卡利丁,C.R.(1982年)《分子生物学杂志》161卷,343 - 352页],认为这一普遍规律的失效是沿着寡核苷酸双螺旋发生螺旋扭曲的结果。磷酸基团位置关系的显著例外是5'-Py - Pu - 3'二核苷酸序列,其共振场强低于预期,这与奥特和埃克斯坦报道的类似结果一致[奥特,J.,& 埃克斯坦,F.(1985年)《生物化学》24卷,253页]。14聚体的³¹P化学位移值与卡利丁的螺旋扭曲总和函数之间存在合理的相关性。³¹P谱中最不寻常的³¹P共振峰出现在最上场位置,已将其归属为从5'端起的第二个磷酸基团位置(5'-GpT - 3')。这种不寻常的化学位移可能是由于在14聚体序列中该位置预测会出现较大的螺旋扭曲角。此外,据信这种大的螺旋扭曲代表了一种独特的结构特征,它是乳糖阻遏蛋白与这个14聚体乳糖假操纵基因片段之间实现最佳结合接触的原因。质子共振峰的归属是通过适用于右手B - DNA的二维¹H - ¹H核Overhauser效应(NOESY)连接性,结合二维同核和异核J相关光谱(¹H - ¹H COSY和³¹P - ¹H HETCOR)按顺序进行的。大多数非交换碱基质子和脱氧核糖质子(除了一些未分辨的H4'、H5'和H5"质子)的共振峰已被归属。

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