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Fluorescence detection of thymidine-related single-nucleotide polymorphisms by 3, 5-diaminopyrazine derivatives
Author(s) -
Chunxia Zhao,
Qing Dai,
Takehiro Seino,
Ying-Yu Cui,
Seiichi Nishizawa,
Norio Teramae
Publication year - 2005
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/49.1.221
Subject(s) - thymine , fluorescence , chemistry , nucleotide , dna , ligand (biochemistry) , base pair , ap site , hydrogen bond , binding site , stereochemistry , molecule , biochemistry , endonuclease , gene , receptor , organic chemistry , quantum mechanics , physics
We report on a highly selective fluorescence ligand for thymine (T) base opposite an abasic site (AP site) in DNA duplexes. From the examination of the binding behaviors in solutions buffered to pH 7.0, we find that 6-chloro-3,5-diamino-2-pyrazinecarbonitrile (CDPC) can selectively recognize T with high affinity (Ka = 2.9 x 10(5) M(-1)), and the fluorescence intensity at 424 nm is significantly quenched only when binding to T. It is highly likely that the selective interaction of CDPC with T is explained by a pseudo-base pairing, for which three point hydrogen bonds are formed along the Watson-Crick edge of the target T. These binding functions of CDPC at the AP site are presented to develop ligand-based fluorescence assay for SNPs (single-nucleotide polymorphisms) typing.

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