期刊
BIOCHIMIE
卷 92, 期 4, 页码 370-377出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biochi.2010.01.003
关键词
G-quadruplex; I-motif; Telomeres; Selectivity; Ruthenium
资金
- National China [20901060, 20871094]
- Natural Science Foundation
Inspired by the enormous importance attributed to the structure and function of human telomeric DNA, we focus our attention on the interaction of [Ru(bpy)(2)(dPPz)(2+) with the guanine-rich single-strand oligomer 5'-AGGGTTAGGGTTAGGGTTAGGG-3' (22AG) and the complementary cytosine-rich strand (22CT). In Na+ buffer, 22AG may adopt an antiparallel basket quadruplex, whereas, it favours a mixed parallel/antiparallel structure in K+ buffer. 22CT may self-associate at acidic pH into an i-motif. In this paper, the interaction between [Ru(bpy)(2)(dPPz)(2+) and each unusual DNA was evaluated. It was interesting that [Ru(bpY)(2)(dPPz)(2+) could promote the human telomeric repeat 22AG to fold into intramolecular antiparallel G-quadruplex without any other cations. What's more, [Ru(bpy)(2)(dppz)(2+)] was found to have a strong preference for binding to G-quadruplexes that were induced through either Na+ or K+, while weak binding to i-motif was observed. The results also indicated that [Ru(bpY)(2)(dPPz)(2+) could serve as a prominent molecular light switch for both G-quadruplexes, revealing a potential application of the title complex in luminescent signaling of G-quadruplex DNA. (C) 2010 Elsevier Masson SAS. All rights reserved.
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