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Royal Society of Chemistry, RSC Advances, 9(5), p. 6993-7000, 2015

DOI: 10.1039/c4ra12858c

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Functionalizable red emitting calcium sensor bearing a 1,4-triazole chelating moiety

Journal article published in 2015 by Mayeul Collot, Christian D. Wilms, Jean-Maurice Mallet ORCID
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

Herein we developed a functionalizable OFF-ON red emitting fluorescent calcium probe based on a new chelating system formed by CuAAC click chemistry (Huisgen cycloaddition). The pro-sensor 7 which is not sensitive to Ca, contains an alkyne moiety that, upon the click reaction, forms a chelating group involving the 1,4-triazole. Probe 10 exhibited good sensitivity towards calcium (K = 5.8 μM) and zinc (5.6 μM) with a high dynamic range (65 fold fluorescence increase), high quantum yield (0.59) and showed very low fluorescence enhancement in the presence of a high concentration of Mg. We extended this method and generated two dextran conjugates in order to compare their sensing properties with those of the molecular form of 10.