z-logo
open-access-imgOpen Access
Fluorescence-based affinity labeling of nucleobase by hydrogenbond forming metal complex
Author(s) -
Keitaro Yoshimoto,
H. Atsumi,
Shingo Saito,
Moriya Okuma,
M. Maeda,
Yukio Nagasaki
Publication year - 2007
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/nrm152
Subject(s) - nucleobase , fluorescence , dota , chemistry , moiety , dna , linker , conjugated system , amide , ligand (biochemistry) , stereochemistry , oligonucleotide , lanthanide , chelation , combinatorial chemistry , biochemistry , organic chemistry , polymer , ion , physics , receptor , quantum mechanics , computer science , operating system
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom