Characterization of the hydrogen bond network in guanosine quartets by internucleotide 3hJNC′ and 2hJNN scalar couplings

被引:66
作者
Dingley, AJ
Masse, JE
Feigon, J [1 ]
Grzesiek, S
机构
[1] Univ Basel, Biozentrum, Dept Biol Struct, CH-4056 Basel, Switzerland
[2] Univ Dusseldorf, Inst Phys Biol, D-40225 Dusseldorf, Germany
[3] Forschungszentrum Julich, Inst Biol Struct, D-52425 Julich, Germany
[4] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
base pairs; DNA; hydrogen bond; nucleic acid; quadruplex; scalar coupling;
D O I
10.1023/A:1008307115641
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Scalar coupling correlations across hydrogen bonds with carbonyl groups as acceptors have been observed in a variety of proteins, but not in nucleic acids. Here we present a pulse scheme that allows such an observation and quantification of trans-hydrogen bond (3h)J(NC') correlations in nucleic acid base pairs, between the imino nitrogen (15)N1 and the carbonyl (13)C6 nuclei within the guanine quartets of the Oxy-1.5 DNA-quadruplex. Intra- and internucleotide N-H ... O=C connectivities can be traced around each guanine quartet, allowing the hydrogen bonding partners to be unambiguously assigned. Absolute values of the (3h)J(NC') couplings are approximately 0.2 Hz as quantified by a selective long-range H(N)CO experiment and are thus on average smaller than the analogous (3h)J(NC') couplings observed in proteins. In addition, an improved version of the pseudo-heteronuclear H(N)N-COSY [Majumdar et al. (1999) J. Biomol. NMR, 14, 67-70] is presented which allows simultaneous detection of the N-15-donor and N-15-acceptor resonances connected by (2h)J(NN) couplings in hydrogen bonds involving amino groups. Using this experiment, values ranging between 6 and 8 Hz are determined for the (2h)J(NN) couplings between (15)N2 and (15)N7 nuclei in the guanine quartet. These values are not strongly influenced by the presence of a significant amount of chemical exchange broadening due to amino group rotations.
引用
收藏
页码:279 / 289
页数:11
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