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Red-shifted fluorescent aminated derivatives of a conformationally locked GFP chromophore.

Authors :
Baranov MS
Solntsev KM
Baleeva NS
Mishin AS
Lukyanov SA
Lukyanov KA
Yampolsky IV
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2014 Oct 06; Vol. 20 (41), pp. 13234-41. Date of Electronic Publication: 2014 Aug 29.
Publication Year :
2014

Abstract

A novel class of fluorescent dyes based on conformationally locked GFP chromophore is reported. These dyes are characterized by red-shifted spectra, high fluorescence quantum yields and pH-independence in physiological pH range. The intra- and intermolecular mechanisms of radiationless deactivation of ABDI-BF2 fluorophore by selective structural locking of various conformational degrees of freedom were studied. A unique combination of solvatochromic and lipophilic properties together with "infinite" photostability (due to a dynamic exchange between free and bound dye) makes some of the novel dyes promising bioinspired tools for labeling cellular membranes, lipid drops and other organelles.<br /> (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-3765
Volume :
20
Issue :
41
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
25171432
Full Text :
https://doi.org/10.1002/chem.201403678