| Literature DB >> 24616292 |
Pablo Rivera-Fuentes1, Stephen J Lippard.
Abstract
A reversible, reaction-based sensor for biological mobile zinc was designed, prepared, and characterized. The sensing mechanism of this probe is based on the zinc-induced, ring-opening reaction of spirobenzopyran to give a cyanine fluorophore that emits in the deep-red region of the electromagnetic spectrum. This probe is not activated by protons and operates efficiently in aqueous solution at pH 7 and high ionic strength. The mechanism of this reaction was studied by using a combination of kinetics experiments and DFT calculations. The biocompatibility of the probe was demonstrated in live HeLa cells.Entities:
Keywords: bioinorganic chemistry; biosensors; coordination chemistry; spirobenzopyran
Mesh:
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Year: 2014 PMID: 24616292 PMCID: PMC4037373 DOI: 10.1002/cmdc.201400014
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466