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Design and Development of a Two-Color Emissive FRET Pair Based on a Photostable Fluorescent Deoxyuridine Donor Presenting a Mega-Stokes Shift.

Authors :
Barthes NP
Gavvala K
Bonhomme D
Dabert-Gay AS
Debayle D
Mély Y
Michel BY
Burger A
Source :
The Journal of organic chemistry [J Org Chem] 2016 Nov 18; Vol. 81 (22), pp. 10733-10741. Date of Electronic Publication: 2016 Oct 31.
Publication Year :
2016

Abstract

We report the synthesis and site-specific incorporation in oligodeoxynucleotides (ODNs) of an emissive deoxyuridine analog electronically conjugated on its C5-position with a 3-methoxychromone moiety acting as a fluorophore. When incorporated in ODNs, this fluorescent deoxyuridine analog exhibits remarkable photostability and good quantum yields. This deoxyuridine analog also displays a mega-Stokes shift, which allows for its use as an efficient donor for FRET-based studies when paired with the yellow emissive indocarbocyanine Cy3 acceptor.

Details

Language :
English
ISSN :
1520-6904
Volume :
81
Issue :
22
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
27723328
Full Text :
https://doi.org/10.1021/acs.joc.6b01807