Best method to determine DNA G-quadruplex folding: The 1H-13C HSQC NMR experiment

被引:4
作者
Dickerhoff, Jonathan [1 ]
Jang, Jinho [1 ]
Yang, Danzhou [1 ,2 ,3 ]
机构
[1] Purdue Univ, Coll Pharm, Borch Dept Med Chem & Mol Pharmacol, 575 Stadium Ave, W Lafayette, IN 47907 USA
[2] Purdue Inst Canc Res, 201 S Univ St, W Lafayette, IN 47906 USA
[3] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
基金
美国国家卫生研究院;
关键词
NMR; G-quadruplex; HSQC; Folding; Glycosidic conformation; SPECTROSCOPY; INSIGHTS; SHIFTS; K+;
D O I
10.1016/j.ymeth.2023.11.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
NMR spectroscopy is the major method for G-quadruplex structure determination under physiologically relevant solution conditions. Unlike duplex B-DNA, in which all nucleotides adopt an anti glycosidic conformation, the core tetrad-guanines in a G-quadruplex can adopt anti or syn glycosidic conformation depending on the folding structure. An experimental method that can clearly and unambiguously determine syn and anti tetrad-Gs in a G-quadruplex is highly desirable and necessary. In the present study, we exploit the advantages of the 1H-13C HSQC experiment to determine tetrad-G's glycosidic conformation and thus folding topology of G-quadruplexes. We use several examples to demonstrate the clear and straightforward determination of the guanine glycosidic conformations and G-quadruplex folding structures. Moreover, 1H-13C HSQC data can readily identify adenine H2 resonances as well as determine unusual syn conformation in loop and flanking sequences, a challenging task by standard 2D NOESY.
引用
收藏
页码:35 / 41
页数:7
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