A Simple Method for Getting Standard Error on the Ratiometric Calcium Estimator
Abstract
1.The ratiometric fluorescent calcium indicator Fura-2 plays a fundamental role in the investigation of cellular calcium dynamics. Despite of its widespread use in the last 30 years, only one publication [2] proposed a way of obtaining confidence intervals on fitted calcium dynamic model parameters from single calcium transients. Shortcomings of this approach are its requirement for a 3 wavelengths protocol (excitation at 340 and 380 nm as usual plus at 360 nm, the isosbectic point) as well as the need for an autofluorence / background fluorescence model at each wavelength. We propose here a simpler method that eliminates both shortcommings: O_LIa precise estimation of the standard errors of the raw data is obtained first, C_LIO_LIthe standard error of the ratiometric calcium estimator (a function of the raw data values) is derived using both the propagation of uncertainty and a Monte-Carlo method. C_LI Once meaningful standard errors for calcium estimates are available, standard errors on fitted model parameters follow directly from the use of nonlinear least-squares optimization algorithms. 2. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=158 SRC="FIGDIR/small/424015v1_fig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@c830a6org.highwire.dtl.DTLVardef@f20cbforg.highwire.dtl.DTLVardef@122fb2aorg.highwire.dtl.DTLVardef@197b331_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure 1:C_FLOATNO How to get error bars on the ratiometric calcium estimator? The figure is to be read clockwise from the bottom right corner. The two measurements areas (region of interest, ROI, on the cell body and background measurement region, BMR, outside of the cell) are displayed on the frame corresponding to one actual experiment. Two measurements, one following an excitation at 340 nm and the other following an excitation at 380 nm are performed (at each time point) from each region. The result is a set of four measures: adu340 (from the ROI), adu340B (from the BMR), adu380 and adu380B. These measurements are modeled as realizations of Gaussian random variables. The fact that the measurements as well as the subsequent quantities derived from them are random variable realization is conveyed throughout the figure by the use of Gaussian probability densities. The densities from the MRB are tighter because there are much more pixels in the MRB than in the ROI (the standard deviations of the densities shown on this figure have been enlarged for clarity, but their relative size has been preserved, the horizontal axis in black always starts at 0). The key result of the paper is that the standard deviation of the four Gaussian densities corresponding to the raw data (bottom of the figure) can be reliably estimated from the data alone, [Figure 1], where V is the product of the CCD chip gain squared by the number of pixels in the ROI by the CCD chip readout variance. The algebric operations leading to the estimator (top right) are explicitely displayed. The paper explains how to compute the standard deviation of the derived distributions obtained at each step of the calcium concentration estimation. C_FIG Method nameStandard error for the ratiometric calcium estimator
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- FWCI
- 0.11
- Field percentile
- 39th percentile
- Assay
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A 340/380 nm Light Emitting Diode Illuminator For Fura-2 AM Ratiometric Ca2+ Imaging Of Live Cells With Better Than 5 nM Precision
Peter W. Tinning, Aimée J P M Franssen, … Gail McConnell·Journal of MicroscopyPeer-reviewed·Aug 24, 2017
- Nonlinear super-resolution signal processing allows intracellular tracking of calcium dynamics
Niccolò Calcini, Angélica da Silva Lantyer, … Tansu Celikel·Journal of Neural EngineeringPeer-reviewed·Apr 22, 2024
- A ratiometric ER calcium sensor for quantitative comparisons across cell types and subcellular regions
Ryan J. Farrell, S. Thomas Hennigan, … Timothy A. Ryan·The Journal of General PhysiologyPeer-reviewed·Jul 25, 2026
- A turquoise fluorescence lifetime-based biosensor for quantitative imaging of intracellular calcium
F. H. van der Linden, E. K. Mahlandt, … J. Goedhart·bioRxiv·Jun 21, 2021
- jYCaMP: An optimized calcium indicator for two-photon imaging at fiber laser wavelengths
Manuel Alexander Mohr, Daniel Bushey, … Kaspar Podgorski·Nature MethodsPeer-reviewed·May 25, 2020
- Precise calcium-to-spike inference using biophysical generative models
Gerard Joey Broussard, Giovanni Diana, … Samuel S.‐H. Wang·bioRxiv·Dec 31, 2024