Discrimination of single-nucleotide alterations by G-specific fluorescence quenching

被引:53
作者
Dohno, C
Saito, I [1 ]
机构
[1] Nihon Univ, Sch Engn, NEWCAT Inst, Koriyama, Fukushima 8638642, Japan
[2] Kyoto Univ, Fac Engn, Dept Synthet Chem & Biol Chem, Kyoto 6158510, Japan
[3] Japan Sci & Technol Corp, SORST, Kawaguchi, Saitama 3320012, Japan
关键词
base flipping; bioorganic chemistry; guanine; intercalation; mismatches; pyrene;
D O I
10.1002/cbic.200400325
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
A new strategy for the detection of single-base alterations through fluorescence quenching by guanine Q is described. We have devised a novel base-discriminating fluorescent (BDF) nucleoside, 4'PyT that contains a pyrenecorboxamide fluorophore at the thymidine sugar's C4'-position. 4'PyT-containing oligodeoxynucleotides only exhibited enhanced fluorescence in response to the presence of a complementary adenine base. In contrast, the fluorescence of mismatched duplexes containing 4'PyT/ N base pairs (N = C, G, or T) was considerably weaker. This highly A-selective fluorescence was a product of guanine-specific quenching efficiency; when the complementary base to 4'PyT was a mismatch, the pyrenecarboxamide fluorophore was able to interact intimately with neighboring G bases (the most likely interaction in the case of intercalation), so effective quenching by the G bases occurred in the mismatched duplexes. In contrast, duplexes containing 4'PyT/A base pairs exhibited strong emission, since in this case the fluorophores were positioned in the minor groove and able to escape fluorescence quenching by the G bases.
引用
收藏
页码:1075 / 1081
页数:7
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