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[通过核磁共振谱镧系位移法研究水溶液中的核苷酸构象]

[Nucleotide conformation in aqueous solutions by the NMR spectrum lanthanide shift method].

作者信息

Babushkina T A, Buikliskiĭ V D, Zolin V F, Koreneva L G, Sheveleva I S

出版信息

Biofizika. 1981 Mar-Apr;26(2):187-92.

PMID:7260123
Abstract

Nucleoside triphosphates, ATP in particular, are investigated by 1H and 31P NMR with lanthanide perchlorate as LSR. The nucleotide base is shown to be near the phosphate groups. Dinucleotides and nucleoside monophosphates are investigated by means of a new LSR--lanthanide complex of pirydoxalidenaspartic acid. NAD+ and its derivatives are shown to exist in folded conformation at high pH values. AMP is shown to undergo conformational change in the pH range between 7 and 8.5. The structure of adduct of new LSR with amino acid is calculated in assumption of unaxial symmetry of the magnetic dipolar interaction. Parameters of the interaction were determined from optical spectra.

摘要

以高氯酸镧作为纵向弛豫试剂(LSR),通过1H和31P核磁共振对三磷酸核苷,特别是三磷酸腺苷进行了研究。结果表明核苷酸碱基靠近磷酸基团。利用一种新的纵向弛豫试剂——吡哆醛天冬氨酸镧配合物对二核苷酸和单磷酸核苷进行了研究。结果表明,在高pH值下,NAD+及其衍生物以折叠构象存在。结果表明,AMP在pH值为7至8.5的范围内会发生构象变化。在磁偶极相互作用单轴对称的假设下,计算了新型纵向弛豫试剂与氨基酸加合物的结构。相互作用参数由光谱确定。

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