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PMID: 11175727 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

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

Nature biotechnology ·Vol. 19 ·No. 2 ·2001-02-00 ·Pages 137-41

Nakai J, Ohkura M, Imoto K

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.

MeSH Terms
Adenosine Triphosphate/pharmacology Amino Acid Sequence Animals Calcium/analysis,metabolism Carbachol/pharmacology Cell Line Chickens Edetic Acid/pharmacology Green Fluorescent Proteins Humans Indicators and Reagents Ionomycin/pharmacology Kidney Kinetics Luminescent Proteins/analysis,genetics,metabolism Molecular Sequence Data Mutagenesis, Site-Directed Myosin-Light-Chain Kinase/genetics,metabolism Myosins/chemistry,genetics Peptide Fragments/chemistry,metabolism Recombinant Proteins/analysis,metabolism Transfection
Chemicals
Indicators and Reagents Luminescent Proteins Peptide Fragments Recombinant Proteins Green Fluorescent Proteins Ionomycin Adenosine Triphosphate Carbachol Edetic Acid Myosin-Light-Chain Kinase Myosins Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nakai J
Department of Information Physiology, National Institute for Physiological Sciences, Myodaiji, Okazaki, 444-8585, Japan. [email protected]
Ohkura M
Imoto K
Article Info
Journal
Nature biotechnology
Abbr.
Nat Biotechnol
ISSN
1087-0156
Published
2001-02-00
Pages
137-41
Language
English
Region
United States
NLM ID
9604648
Subset
IM
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