Recent Progress in Abasic Site-binding Small Molecules for Detecting Single-base Mutations in DNA

被引:10
作者
Nishizawa, Seiichi [1 ]
Sato, Yusuke [1 ]
Teramae, Norio [1 ]
机构
[1] Tohoku Univ, Grad Sch Sci, Dept Chem, Aoba Ku, Sendai, Miyagi 9808578, Japan
关键词
DNA recognition; ligand design; biosensors; surface plasmon resonance; fluorescent probes; noncovalent interactions; nucleobases; SURFACE-PLASMON RESONANCE; OPPOSITE AP SITES; SELECTIVE BINDING; IMAGING MEASUREMENTS; NUCLEOBASE RECOGNITION; FLUORESCENCE DETECTION; CYTOSINE OPPOSITE; ADENINE OPPOSITE; DUPLEXES; LIGAND;
D O I
10.2116/analsci.30.137
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This review addresses our recent efforts to design AP site-binding small ligands for SNP (single-nucleotide polymorphisms) typing. First, we present a surface plasmon resonance (SPR) biosensor carrying a derivative of 3,5-diaminopyrazines. Comparison with a bulk assay based on 3,5-diaminopyrazines-DNA binding shows that the immobilization of 3,5-diaminopyrazines on the SPR sensor allows a more sensitive detection of the target DNA, and binding selectivity can be tuned by controlling salt concentrations of the sample solutions. We also present a ratiometric fluorescent probe, in which an environmentally sensitive fluorescent dye, a benzofurazan derivative, is linked through an alkyl spacer to a 2-amino-1,8-naphthyridine derivative. The binding and sensing properties of these systems are discussed as a basis for the advanced design of DNA-binding small molecules for gene detection.
引用
收藏
页码:137 / 142
页数:6
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