Article

Fluorescence-based affinity labeling of nucleobase by hydrogen-bond forming metal complex.

Department of Materials Science, Graduate School of Pure and Applied Sciences, Center for Tsukuba Advanced Research Alliance (TARA), University of Tsukuba, 1-1-1 Ten-noudai, Tsukuba, Ibaraki 3058573, Japan.
Nucleic Acids Symposium Series 02/2007; DOI:10.1093/nass/nrm152 pp.303-4
Source: PubMed

ABSTRACT A new class of nucleobase-binding fluorescent ligand, ND-DOTA in which 2-amino-5,7-dimethyl-1.8-naphthyridine (ND) is conjugated with 1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid (DOTA) by an amide linker, was synthesized. On the basis of the experimental results obtained from the DNA melting analysis and fluorescent measurement, ND-DOTA-Tb (III) complex was found to strongly recognize cytosine (C) base opposite an abasic site in DNA duplexes. The binding of ND-DOTA-Tb (III) with C was accompanied by significant quenching of the fluorescence from the naphthyridine moiety (lambdamax, 435 nm), while the emission from the Tb based on lanthanoids energy-transfer luminescence (lambdamax, 550 nm) was relatively unaffected. Such a fluorescence response of ND-DOTA-Tb (III) is to be expected to develop the fluorescence-based affinity labelling of a nucleobase at the single-nucleotide segments in DNA duplexes.

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Keywords

amide linker
 
cytosine
 
experimental results
 
fluorescence
 
fluorescence response
 
fluorescence-based affinity labelling
 
fluorescent measurement
 
lambdamax
 
lanthanoids energy-transfer luminescence
 
ND-DOTA
 
ND-DOTA-Tb
 
new class
 
nucleobase-binding fluorescent ligand
 
significant quenching
 
single-nucleotide segments
 
synthesized
 

Keitaro Yoshimoto