Literature DB >> 11175727

A high signal-to-noise Ca(2+) probe composed of a single green fluorescent protein.

J Nakai1, M Ohkura, K Imoto.   

Abstract

Recently, several groups have developed green fluorescent protein (GFP)-based Ca(2+) probes. When applied in cells, however, these probes are difficult to use because of a low signal-to-noise ratio. Here we report the development of a high-affinity Ca(2+) probe composed of a single GFP (named G-CaMP). G-CaMP showed an apparent K(d) for Ca(2+) of 235 nM. Association kinetics of Ca(2+) binding were faster at higher Ca(2+) concentrations, with time constants decreasing from 230 ms at 0.2 microM Ca(2+) to 2.5 ms at 1 microM Ca(2+). Dissociation kinetics (tau approximately 200 ms) are independent of Ca(2+) concentrations. In HEK-293 cells and mouse myotubes expressing G-CaMP, large fluorescent changes were observed in response to application of drugs or electrical stimulations. G-CaMP will be a useful tool for visualizing intracellular Ca2+ in living cells. Mutational analysis, together with previous structural information, suggests the residues that may alter the fluorescence of GFP.

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Year:  2001        PMID: 11175727     DOI: 10.1038/84397

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  536 in total

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Review 5.  Imaging calcium signals in vivo: a powerful tool in physiology and pharmacology.

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Review 10.  Mitochondrial Ca2+ concentrations in live cells: quantification methods and discrepancies.

Authors:  Celia Fernandez-Sanz; Sergio De la Fuente; Shey-Shing Sheu
Journal:  FEBS Lett       Date:  2019-05-18       Impact factor: 4.124

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