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13C标记的寡脱氧核糖核苷酸:人腺病毒核因子I识别位点含CCAAT序列的溶液研究

13C-labeled oligodeoxyribonucleotides: a solution study of a CCAAT-containing sequence at the nuclear factor I recognition site of human adenovirus.

作者信息

Wu J, Serianni A S

机构信息

Department of Chemistry and Biochemistry, University of Notre Dame, Indiana 46556.

出版信息

Biopolymers. 1994 Sep;34(9):1175-86. doi: 10.1002/bip.360340907.

Abstract

The solution behavior of the single-stranded CCAAT-containing octamer 1, d(AGCCAATA), that comprises part of the nuclear factor I (NF-I) recognition site at the origin of replication of human adenovirus has been studied by nmr spectroscopy at 500 and 600 MHz. Proton resonance assignments for 1 were aided by selective 13C enrichment at C1' of A1 or A5. High-resolution 13C-1H heteronuclear multiple-bond coherence spectra of the 13C-labeled oligomers permitted the selective detection of furanosyl ring protons within each labeled residue due to short- and long-range 13C-1H couplings to the enriched C1'. The resulting assignments provided firm starting points in the interpretation of double quantum filtered correlated spectra, yielding information supplemented by total correlated spectroscopy (TOCSY) and rotating frame nuclear Overhauser effect spectroscopic data to completely assign the 1H-nmr spectrum of 1 and extract 3JHH values for furanose conformational analysis. Several 13C-1H spin-coupling constants within the 13C-enriched A1 or A5 residues were measured from cross-peak shifts in TOCSY spectra, and their signs determined by inspection of the relative orientations of these shifts. 1H-1H and 13C-1H spin-couplings both indicate a preference (> 75%) for south (C2'-endo) conformations by the furanosyl rings of 1.

摘要

已通过500兆赫和600兆赫的核磁共振光谱法研究了单链含CCAAT的八聚体1(d(AGCCAATA))的溶液行为,该八聚体构成了人类腺病毒复制起点处核因子I(NF-I)识别位点的一部分。通过在A1或A5的C1'处进行选择性13C富集辅助了对1的质子共振归属。13C标记的寡聚体的高分辨率13C-1H异核多键相干光谱,由于与富集的C1'存在短程和长程13C-1H耦合,使得能够选择性检测每个标记残基内的呋喃糖环质子。所得的归属为解释双量子滤波相关光谱提供了坚实的起点,所产生的信息通过全相关光谱法(TOCSY)和旋转框架核Overhauser效应光谱数据进行补充,以完全归属1的1H核磁共振光谱并提取用于呋喃糖构象分析的3JHH值。通过TOCSY光谱中的交叉峰位移测量了13C富集的A1或A5残基内的几个13C-1H自旋耦合常数,并通过检查这些位移的相对取向确定了它们的符号。1H-1H和13C-1H自旋耦合均表明1的呋喃糖环优先选择(>75%)南(C2'-内型)构象。

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