Analysis of FRAP Curves
For K_FRAPcalcV8.ipf (IgorPro)
- IgorPro (Wavemetrics) Procedure Language
- Import FRAP measurement tab-delimited text files of
Zeiss data format
Leica data format
tab-delimited FRAP measurements (with 6 controls).
- Three different ways of normalizing FRAP curve
- Curve fitting by single and double exponential formula and 2 diffusion formula.
- Correction for the acquisition bleaching.
- Output of half-max, diffusion coefficient, mobile/immobile fractions.
- Weighting for the fitting.
- Evaluation of goodness of fit by chi-square and gamma function.
- Graphing of the fitted curve and estimation curve without acquisition bleaching.
1.2.1. Chemical Interaction Models
188.8.131.52 Chemical Interactions with immobile entity (not finished)
1.2.2. Diffusion models (not finished)
1.2.3. Reaction-Diffusion Models
2.6. Fitting Procedure
2.6.5. Soumpasis Diffusion Fitting
2.6.6. Ellenberg Diffusion Fitting
3. Work Flow
3.2. Importing Frap Data
Interpretation of FRAP curves can be qualitative for a simple comparison of several different experiment results. Just by looking at the graph, the speed of recovery its plateau level can be examined. For example, Figure 1-1 shows several FRAP curves derived from cells under different experimental treatments.
The recovery of blue curves is much faster than the red curve. We can then say that the mobility of the observed molecule is faster in the blue curve conditions than the red curve condition. The plateau level seems to be also different in two conditions. Blue curve plateau is higher than that of the red curve. We then know that the mobile fraction (see below) of the molecule is larger in the blue conditions than in the red condition.
To add a bit more quantitative taste, we can measure these two features numerically from the FRAP curves. An example of actual FRAP curve after normalization is shown in Figure 1-2.
The FRAP recovery curve do not always reach the level of original fluorescence intensity. The plateau level (Fig. 1-2 a) is often lower than the pre-bleach fluorescence intensity because some of the FRAP-bleached molecule are immobile within the FRAP ROI that they do not contribute to the recovery and at the same time do not give away free binding sites for incoming un-bleached proteins. For these reasons, fraction of proteins that contribute to the recovery are called ‘mobile fraction’ and those do not are called ‘immobile fraction’ and each corresponds to a and b (=1-a) in figure 1-2, respectively. Conventionally used index for the speed of recovery is the time it takes for the curve to reach 50% of the plateau fluorescence intensity level (c) and is called ‘half maximum’ or ‘half life’ and often abbreviated as ‘τ1/2’(d). Shorter half max tells us that the recovery is faster.
A more objective way to extract half max and mobile / immobile fraction is to fit the normalized FRAP curve I(t) by an exponential equation
The fitted coefficients can be used for calculating following parameters of the FRAP curve:
Mobile fraction = A (1-2)
Immobile fraction = 1-A (1-3)
Half Max: (1-4)
For any kind of molecules within biological system, two major factors affect their mobility. First is diffusion. Diffusion of the molecule drives the change in the position of the molecule from time to time. Rate of diffusion is determined by the diffusion constant of the molecule, which is affected by the size of the molecule, viscosity and temperature of the surrounding medium. Physical structures that hinder their pure diffusion can also be considered as another factor and can be considered as a parameter for the apparent viscosity of the medium (cf. Luby-Phelps). Second is the chemical interaction. The environment of molecule is rarely a pure solvent in biological system. These surrounding molecular species interact with the observed molecule. Binding and dissociation, namely the binding constants of the molecule with others, affects the mobility of the molecule. Therefore FRAP recovery curve is determined by two major factors.
If the diffusion of the molecule is fast and the interaction of molecule is slow, then the rate limiting factor for the mobility is the interaction. In this case, we assume that the FRAP recovery curve is dominated by the chemical interaction. If the interaction of the molecule is faster than the diffusion, then the mobility of the molecule is dominated by the diffusion.
Choice of equation for fitting the recovery curve of FRAP (Fluorescence Recovery After Photobleaching) experiments depends on what you assume for the mobility of the protein that you are studying. There are three different models. (1) Chemical Interaction Model (2) Diffusion Model (3) Reaction-Diffusion model.
FRAP curves are fitted with exponential equation in chemical interaction models,. In the simplest case, the equation is with a single exponential term and called “single exponential equation” and was already introduced above as equation (1).
The exponential equation is an analytical solution of a two-compartment model (Jacquez, 1972). We consider molecule in one chamber A. The concentration of the molecule is [A] and the molecule is moving to the neighboring chamber B though a narrow channel that connects two chambers as shown in the illustration below (Figure 3.).
Figure 3. Compartmental Model of a Simple Chemical Interaction
If the rate constant of transition from A to B is ka and from B to A is kb, then the rate of the change of the molecule concentration in the chamber B is
Solving this equation using parameter variations and assuming that [B]=0 when t=0, yields exponential equation (1-1) with
The interaction of observed molecule is not necessarily limited to a single interaction. If the molecule we are observing possesses two independent binding sites, then there are two interactions.
Although the interactions are independent, we observe fluorescence recovery that is sum of these two interactions…(to becontinued)
Double exponential equation arises also in other cases. For example, the interaction could be in two steps such that the molecule interacts first weakly, and then upon this weak interaction will there be a strong interaction.
Ka, Kb, Kc and Kd are rate constants. Although the state of interaction is different, binding in weak and strong forms both contribute to the recovery of the fluorescence. Thus the recovery curve is
Since source of fluorescence outside the FRAP ROI is enormous, we assume that [A] is always constant.
[Bw] and [Bs] increases with time. The rates of increase of the molecule with each binding state are
Solving these coupled differential equations, we obtain a double exponential equation
184.108.40.206 Chemical Interactions with immobile entity.
(Recovery depends only on Koff)
1.2.2. Diffusion models
(Ellenberg et al., 1997)
Note that the shape of the FRAP-ROI affects the recover kinetics largely. Each fitting equation assumes certain shapes for the FRAP-ROI. The area of the FRAP-ROI also matters so you must do the experiment with a constant FRAP-ROI area.
Any molecular mobility has both Reaction and diffusion components. Above two models are simplifies this reality by assuming that one of these two components is negligible. Logically including both components would be the ultimate direction of the modeling-based fitting (Sprague and McNally, 2005; Sprague et al., 2004). This model is not implemented yet in the program.
Following four different regions are recommended to be measured for each experiment (see Figure 4).
(1) FRAP ROI (ROI=Region Of Interest). Region where you actually bleached the fluorophore by strong laser irradiation. Shape and size of the bleaching must be controlled. Shape of the FRAP ROI, circular, rectangular, affects the model equation to be fitted with. Size of the ROI matters with the diffusion-limited type of FRAP recovery (see below).
(2) Reference ROI Also called ‘Cell Part’. ROI within the same cell (or it could be other cell) to measure a decay in fluorescence due to the acquisition bleaching. The result could be erroneous (see xx for more explanation).
(3) Base ROI Also called ‘background’. Set ROI outside the cell, where there should be no fluorescence, to know the offset intensity.
(4) Whole Cell ROI or ‘All cell’. The average fluorescence intensity of the whole cell you are observing.
Figure 4 Fluorescence intensity kinetics at four different positions (courtesy of Mei Rosa Ng).
Red: FRAP, Blue: Part of cell, Purple: Whole Cell and Black: Base line
The minimal data set for measuring the proper kinetics is FRAP ROI (1) and BASE ROI(4). It is possible to estimate the recovery kinetics without (4), but if the baseline is high relative to the signal and different from one another experiments, the interpretation of data deviates largely from the reality. Complete set of data is all four different ROI.
For numerical treatments of FRAP recovery curves, several technical terms are used. See also Figure 5 and 6.
1. Intensity measurements from different ROIs
FRAP ROI: Ifrap(t)
Reference ROI: Iref(t)
Base ROI: Ibase(t)
Whole Cell ROI: Iwhole(t)
2. Intensity of FRAP ROI at bleaching time point tbleach is termed ’frap-bleach intensity’ or Ifrap-bleach.
3. Pre-bleach Intensities
Average fluorescence intensity before FRAP bleaching is obtained by first subtracting the off-set fluorescence intensity (base ROI intenisty) from other curves and averaging the value for pre-bleach period:
- FRAP pre-bleach intensity: Ifrap-pre
- Reference pre-bleach intensity: Iref-pre
- Whole Cell pre-bleach intensity: Iwhole-pre
- Whole Cell post-bleach intensity: Iwhole-post
Average intensity of the Whole cell ROI after the bleaching. Use 10 time points after the bleaching.
fprebleach is the frame (sampling) number during pre-bleach period.
Figure 5 Terms used in FRAP recovery curve analysis
5. The ratio Iwhole-post / Iwhole-pre is called ‘gap ratio’ (see Figure 6). This ratio is an indicator of the amount of fluorescence that is lost form the cell by FRAP-bleaching. See section 2.6 ‘Gap Ratio: Effects of FRAP bleaching on un-FRAPped region’ for details.
Any FRAP curve contains two components of fluorescence intensity changes. The major component is the recovery of fluorescence due to the flux of labeled proteins into the FRAP ROI. The second component is the bleaching of fluorescence everywhere within the microscope field where illumination light is irradiated to excite the fluorophore for measuring their intensity –although very slow, acquisition bleaching causes less and less molecules with fluorescence with time. This acquisition bleaching attenuates the fluorescence recovery, because bleached molecules by this reason also move into the FRAP ROI and attenuate the recovery of fluorescence. Thus, how to correct for acquisition bleaching is one of the key point for the analysis of FRAP curve. In some cases, this correction is included in the normalization procedure but in other cases correction is independent from the normalization procedure. In this latter case, correction will be done by including acquisition bleaching parameters to the FRAP equation for fitting to the measured recovery curve. In the following, I will describe different methods for doing normalizations.
2.3.1. Normalization that involves acquisition bleaching correction This method is known as ‘the double normalization’ (Phair et al., 2004). In double normalization, we take the measurement from whole cell ROI for correcting the acquisition bleaching effects. Average Pre-bleach whole cell intensity divided by the whole cell intensity at each time points in the post-bleach period will be multiplied to the FRAP curve at that time point. Before this operation, both Whole Cell ROI and FRAP ROI data are subtracted by Base ROI intensity.
In the ‘single normalization’ method proposed by Phair et al., FRAP curve is simply subtracted by the offset intensity outside of the cell (Base ROI), and then the base intensity is taken as 0 and pre-bleach intensity Ifrap-pre of the FRAP curve is taken as 1. If whole cell ROI or reference ROI data is not available, then the single normalization method is employed but one should keep in mind that this does not correction for the acquisition bleaching.
In these methods, FRAO curves are normalized to Ifrap-pre that Ifrap-bleach >0. For fitting equations that assumes Ifrap-bleach=Ifrap(tbleach)=0, such as for diffusion-dominant models ‘Ellenbergand ‘Soumpasis’, (2-2) will be further normalized to the full scale.
In this method, Base ROI measurement is not required. Acquisition bleaching will be corrected directly when the curve is fitted, by using parameters for the acquisition bleaching independently acquired through fitting the background decay curve. For more detail, see ‘2.4 Determination of acquisition bleaching parameters’. Following two methods uses this normalization method.
In ‘Rainer’s method’, the background decay curve (either Whole Cell ROI or Reference ROI) will be normalized in the same way as the FRAP ROI.
This calculation may result negative values for the normalized background decay curve but this does not affect the decay parameter. In case of ‘Back Multiply’ method, normalization procedure takes two steps. First, normalize the background curve by
then normalize to the full range by
For obtaining parameters of acquisition bleaching, we assume that the decay of fluorescence intensity follows standard exponential decay.
We fit the measured fluorescence decay to the equation (2-9). As the t approaches infinity, fluorescence level approaches to the base line level y0-decay since all fluorescence will be bleached by time. In case when Whole Cell ROI data is available, then Iwhole(t) will be fitted. If not, then Reference ROI data Iref(t) will be used.
Different Patterns of exponential curves
Figure 7 Different Patterns of exponential curves
Among these combinations, the fitting is successful only when both parameters are positive (a). (b) and (c) parameter combinations results if the decay curve is an increase in the fluorescence intensity by time, indicating that the quality of the measurement is bad. Double negative parameters (d) results only when the curve has downward curvature, which does not happen for the fluorescence decay by acquisition bleaching. For these reasons, when the parameter combination is not double positive (a), the program automatically sets the background flat and will be indicated in the ‘History’ window. One cause for such problems in the fitted curve could come from the data close to the FRAP bleaching time point since they tend to be unstable. You could avoid fitting those time points. Such an option is implemented in the program (adjust “Back Start”).
2.5. Gap Ratio: Loss of fluorescence due to the FRAP bleaching 
When relatively large part of the sample is irradiated for FRAP bleaching, total fluorescence level within the cell will decrease significantly (see Figure 6) by FRAP bleaching. If you are also monitoring other part of the cell by Reference ROI, although the decrease is more gradual, you may detect it as well, because FRAP-bleached molecules moved to the Reference ROI and lowered its fluorescence level (figure 6). The acquisition bleaching which you are observing then contains two components. (a) Bleaching due to illumination light and (b) FRAP bleached molecules moving into the ROI. Effect (b) is a complicated issue. The distance between FRAP ROI and Reference ROI matters with kinetics e.g. closer the distance between two regions, faster that you will detect the decrease. Percentage of the fluorescence that you bleached for FRAP also matters. If the FRAP-bleaching affects the decay of the reference ROI within the cell too much, you need to obtain the acquisition bleaching kinetics from the whole cell. If the effect of FRAP-bleaching on the reference point intensity dynamics is minimal e.g. FRAP-bleached fluorescence is negligible against the total fluorescence of the cell, then you can use the reference ROI for acquisition bleaching correction.
We estimate the amount of fluorescence loss due to the FRAP bleaching by obtaining the ‘Gap Ratio’. This value enables us to calculate more precise mobile / immobile fraction of the molecule.
(1) When you have ‘Whole Cell ROI’ data
If you have average fluorescence intensity changes of the whole cell ROI, then the decrease fluorescence by FRAP bleaching will be calculated by taking the ratio of Iwhole-pre and Iwhole-post.
(2) When ‘AllCell’ data is NOT available
First, we estimate the decay kinetics by fitting the equation (2-9) to post- FRAP bleaching period of Iref(t). Then we estimate the average fluorescence level before the FRAP bleaching by extrapolating the fitted decay curve. This is an estimation from the intensity changes after the loss of fluorescence by FRAP bleaching, so we call this fluorescence level Iref-pre-est. From the experiment, we know the measured fluorescence level before the FRAP bleaching. We average these values and we call it Iref-pre-measured. Iback-pre-est is smaller than Iback-pre-measured because there is a loss in fluorescence due to the FRAP bleaching. Taking the ratio between these two values, we obtain the Gap Ratio.
We use this Gap Ratio for calculating mobile and immobile fraction. The FRAP curve reaches plateau and we detect this plateau level to know the mobile fraction. However, the plateau level never becomes 1 because we bleached certain fraction of molecules by FRAP bleaching, the fraction which is equal to the Gap Ratio. Hence, we calculate the actual mobile fraction by
MobileFractionest = MobileFractionmeasured / Gap Ratio (2-12)
After normalizing and correcting for the acquisition bleaching, FRAP curve is fitted with standard exponential equation as explained in the “chemical interaction dominant” model.
At bleaching time point, I(tbleach) = y0+A and the plateau of the curve is y0. Mobile fraction will be calculated by
and Half-Max calculation is same as the equation (1-4).
The rate of fluorescence recovery is proportional to the available binding sites within the bleached region. Simultaneously the recovery rate is attenuated by fluorescence decay due to acquisition bleaching. This attenuation is proportional to the fluorescence level at each time point. Taken together, the rate of fluorescence recovery is
Imax is a fluorescence intensity corresponding to the maximum available binding site. Imax = Ifrap-pre if all molecules are mobile. is a time constant characteristic to fluorescence recovery, and is a time constant that characterizes acquisition photobleaching. Solving the differential equation (2-15) and taking that Ifrap(tbleach) = 0,
We obtain before these fittings by fitting post-bleach period of Whole Cell ROI or Reference ROI data as explained in details already (see 2.3) and use it as a constant value during fitting. The estimation curve corrected for the acquisition bleaching will then be
For knowing the mobile – immobile fraction, we consider the Gap Ratio as it was already explained (see 2.5 for more detail).
Half-Max calculation is the same as the equation (1-4) using.
The principle of correction for acquisition bleaching is the same as Phair’s method, but instead of scaling each time point of Ifrap(t) by corresponding time point Iwhole(t) or Iref(t), we use three parameters of decay curve for directly fitting the un-corrected FRAP curve. The advantage of this method over Phair’s method is that the amplification of error due to multiplication of two data from each time point does not occur. Amplified error will cause lowering of the Gamma-Q value for the evaluation of the fitting (see 2.7). We fit the normalized, uncorrected FRAP curve by following equation.
, y0, B are obtained by fitting the decay curve, either Whole cell ROI or Reference ROI, that is normalized by the procedure explained already (see 2.3). These three values are taken as constant values during fitting. The estimation curve corrected for the acquisition bleaching will then be
Since decay curve parameters used in (2-20) is the ones from already normalized decay curve, we do not need to consider the Gap Ratio for knowing the mobile fraction.
Mobile = A (2-22)
Half-Max calculation is the same as the equation (1-4) using.
Similar to the single exponential fitting, we fit the FRAP curve by
At bleaching time point, I(tbleach) = y0+A1+A2 and the plateau of the curve is y0. Mobile fraction will be calculated by
We fit double-normalized FRAP curve as explained already (see 2.3) to the theoretical formula for diffusion FRAP curve
where I0() is the modified Bessel function of the first kind of order 0 and I1() is the modified Bessel function of the first kind of first order to find only parameters A and τ. A will be the mobile fraction and the diffusion coefficient is calculated by
where w is the diameter of the circular FRAP ROI and user must know the value. Half maximum of the recovery is estimated from the estimation curve generated by the equation (2-25).
We fit double-normalized FRAP curve as explained already (see 2.3) to the empirical formula
as proposed by Ellenberg et. al. (1998). w is the width of the strip-bleaching and need a user input. The fitting will look for a likely two parameters Ifinal and D, the diffusion coefficient. Ifinal will be considered as the mobile fraction. Half max can be calculated as
If data points are (xi,yi) i=0,….N-1 and the model equation to fit is y(x)=y(x;a0….aM-1), then the maximum likelihood estimate of the equation parameters is obtained by minimizing the chi-square.
Measurement error σ can be obtained from the standard deviation of pre-bleach FRAP intensities. Using chi-square obtained by equation (2-29), chi-square distribution for N-M degree of freedom can be calculated using incomplete gamma function. Then this distribution gives the probability Q that the chi-squared should exceed a particular chi-square by chance.
where υ =N-M is the number of degree of freedom; N is the number of fitted points and M is the number of parameters within equation to fit.
Following is an intuitive explanation: Any measurement results deviate from ‘real values’ due to the measurement error. Probability Q tells you if the chi-square calculated from the fitting results are reasonably within the range of possible measurement errors. Q > 0.1 can be considered a good fit, Q > 0.01 is a moderately good fit, and Q < 0.01 recommends you either to think about different model equation or to narrow down the range for the fitting or ultimately suggesting that something is wrong with the experiment. Q will be printed in the history window as “gammaQ” value.
“…It is for this reason that reasonable experimenters are often rather tolerant of low probabilities Q. It is not uncommon to deem acceptable on equal terms any models with, say, Q > 0.001. This is not as sloppy as it sounds: truly wrong models will often be rejected with vastly smaller values of Q, 10-18, say. However, if day-in and day-out you find yourself accepting model with Q ~ 10-3, you really should track down the cause.”(numerical recipes in C)
File à Open File à Procedure… à (select the file “K_FRAPcalcV8.ipf”) then click “Compile” at the left-bottom corner of the opened window “K_FRAPcalcV8.ipf”. You will see a new menu ‘Frap Calc’ after compiling the program (fig. 3-1).
Fig. 3-1 ‘FrapCalc’ menu
Zeiss and Leica each have their own data output format. The program can import both formats, but the arrangement of data is various. Four different types of fluorescence intensity sampling are possible from FRAP experiments (see 2.1 and 2.2 for more detail) and how they are ordered depends on the user.
(a) FRAP ROI time series
(b) Reference or Cell Part ROI time series
(c) Whole cell or All Cell ROI time series
(d) Base ROI time series
+ Data file also contains time point data. We call this “Time”.
The program has a list of typical arrangements for each company’s data format.
Fig. 3-2 Zeiss data importing
6 different types of data alignments are possible now.
-. 2 columns: Time – Frap
-. 3 columns: Time – FRAP – Cell Part
-. 3 columns: Time – Cell Part – FRAP
-. 8 columns: Time – FRAP – 6 x Cell Part
-. 4 columns: Time – FRAP – All Cell – Base
-. 4 columns: Time – FRAP – Base – All Cell
Fig.3-3 Leica Data Importing
In Leica data format, data for each ROI is separately written in different places within the file. Data first starts with ROI1, with several columns containing frame number, time, channel1 and then channel 2 if there is. Then below ROI1, next ROI2 starts. Four types of arrangements are importable from the program.
-. single channel with three ROIs: FRAP – AllCell – Base
-. double channel with three ROIs: FRAP – AllCell – Base
-. single channel with four ROIs: FRAP – AllCell – Base – Cell Part
-. double channel with four ROIs: FRAP – AllCell – Base – Cell Part
In all cases, when you select one of the importing command, pop up window will appear (Fig. 3-4).
Input any name you like for the experiment (but do not start the name with a number & no space within the name!!). Click “Continue”. Another window pops up to select the data file. Select, and then press OK. Almost immediately, a table and a graph like figure 3-5 will appear. This is the original data. If you selected a data format that does not matches with what you have selected in the menu, then importing is aborted and a warning window appears, telling you how many columns the file contains.
Figure 3-5 shows a snapshot of screen when you import Leica data file with full set of ROI.
3.3.1. Open Fit Panel Frap calc à Fit Panel… This will create a panel shown in the figure 3-6.
3.3.2. Most important procedure before start fitting is user-input of the FRAP bleach point. Check through the table that was automatically opened when you import the file and find out the point number (not time) of the bleaching. Then input the number at the variable setting “Bleach Pnt”. You can toggle the number by clicking the up-down arrow at the right side of the input window.
3.3.3. Using drop-down menu titled ‘experiment’ at the top of the panel, select one of the experiment you imported and named.
3.3.4. Using drop-down menu for ‘Fit Model’ at the second row, select one of the model that you are going to fit. Four different models are possible.
3.3.5. From three different normalization methods, choose one by checking one of the check boxes beside the “Fit model” drop-down menu. Three different normalization methods are possible:
- Phair’s method (Double or Single normalization)
Note: Check buttons will be enabled or disabled automatically depending on the fit model you selected. For example, single exponential model enables all three normalization methods but diffusion models are only possible through Phair’s double normalization.
3.3.6. If you selected Diffusion models, you must enter the “Frap Width”, the size of the FRAP bleached area in µm.
3.3.7. Press ‘Fit!’ button at the left-bottom corner of the panel. This will create a new graph (if there is already a graph window for the corresponding experiment, pressing the button will bring that window forward) and do the fitting. The result is as shown in the figure 3-7 (Rainer’s – Single Exponential), figure 3-8 (Back Multiply – Single Exponential), figure 3-9 (Phair – Single Exponential).
Fig. 3-7 Rainer’s – Single Exponential Blue dots are the decay curve (both Whole Cell and Reference data), Red dots are the FRAP data. Light blue curve is the fitted FRAP curve. Yellow dotted curve shows the estimation curve (see 2.x for details). At the top of the graph, residuals of the fitting are plotted. Inadequate model will result a systematic deviations, as you can see in this figure.
Fig. 3-8 Back Multiply – Single Exponential Blue dots are the decay curve (both Whole Cell and Reference data), Red dots are the FRAP data. Red curve shows the fitting of whole cell data. Light blue curve is the fitted FRAP curve. Yellow dotted curve shows the estimation curve (see 2.x for details). At the top of the graph, fit-residuals
Fig. 3-9 Phair – Single Exponential Red dots are the FRAP data. Light blue curve is the fitted FRAP curve. Decay data are not shown. Yellow dotted curve shows the estimation curve (see 2.x for details). At the top of the graph, fitting residuals are plotted.
3.3.8 Fitted parameters will be indicated in three different places. (1) Within the graph as legends (2) In the history window (3) In the fit Panel. The results printed in the history window looks like figure 3-10.
GammaQ must be first checked to evaluate the fitting (see 2.7). If gammaQ value is less than 0.01, than you must redo fitting either by
(1) Limit the data range for fitting by checking ‘Limit’ check box with Fit Panel and input time points for a desired range. After setting start and end time points, press ‘Fit!’ button again. Alternatively, you can also weight a certain range if you check ‘Weighting’.
(2) Use other fit models and compare gammaQ value. Larger value is better.
If you have a sufficiently large gammaQ, then results can be used as your data. The last
line in the history window is tab delimited in the order of Experiment name – half max –
3.4.1. To print out graph and fitted parameters, do Frap calc à Prepare Layout. This will create a window called “layout” containing both the graph and the results for printing out.
3.4.2. To export fitted parameters as formatted text file, do Frap calc à Export Results as a text file.
3.4.3. To export frap data as formatted text file, do Frap calc à Export Data as a text file.
3.4.4. To do both 3.4.2. and 3.4.3, do Frap calc à Export Results and Data as a text file.
A. Data Format Codes
+ 1111 () 0 FRAP + Whole Cell + Reference + Base
+ 1101 () 1 FRAP + Whole Cell + Base
- 1011 () 2 FRAP + Reference + Base
- 1100 () 3 FRAP + Whole Cell
+ 1010 () 4 FRAP + Reference
- 1001 () 5 FRAP + Base
+ 1000 () 6 FRAP
B. Fit Method Codes
0: Rainer - single exponential
1: BackGroundMultiply-single exponential
2: BackGroundMultiply-double exponential
4: (back multiply Ellenberg diffusion)
5: (back multiply Soumpasis)
6: Double Normalization, single exponential
7: Double Normalization, double exponential
8: Double Normalization Ellenberg
9: Double Normalization Soumpasis
C. Point Number and its content in FittingParameterWave
0: fit method
3: background exists
Ellenberg, J., Siggia, E. D., Moreira, J. E., Smith, C. L., Presley, J. F., Worman, H. J. and Lippincott-Schwartz, J. (1997). Nuclear membrane dynamics and reassembly in living cells: targeting of an inner nuclear membrane protein in interphase and mitosis. J Cell Biol 138, 1193-206.
Jacquez, J. A. (1972). Compartmental analysis in biology and medicine: Elsevier.
Phair, R. D., Gorski, S. A. and Misteli, T. (2004). Measurement of dynamic protein binding to chromatin in vivo, using photobleaching microscopy. Methods Enzymol 375, 393-414.
Soumpasis, D. M. (1983). Theoretical analysis of fluorescence photobleaching recovery experiments. Biophys J 41, 95-7.
Sprague, B. L. and McNally, J. G. (2005). FRAP analysis of binding: proper and fitting. Trends Cell Biol 15, 84-91.
Sprague, B. L., Pego, R. L., Stavreva, D. A. and McNally, J. G. (2004). Analysis of binding reactions by fluorescence recovery after photobleaching. Biophys J 86, 3473-95.
 When base-ROI measurement is not available, the program omits the subtraction of off-set value.
 This section matters only for the “Rainer’s fitting”
 If you are FRAP-bleaching large portion of the total fluorescence, this becomes evident with the acquisition decay curve. There will be a sharp decrease in the fluorescence after you FRAP-bleach. This decrease is not due to the acquisition bleaching but for the reason (b) I mentioned above.
 Function name: K_estGapRFromOrigAllcell(flatback)
 Function Name: K_estGapRFromOrigRef(flatback)
 For the calculation of gap ratio, non-normalized, original decay reference curve is used. This is because with normalized curve, the value could be negative. Since we do not know the intensity offset (baseline), we use 0 in the original curve as the offset value.
 in IgorPro, this is gammaq function
 In the program, one can control the range of FRAP curve to fit using ‘Fit Panel’. See ‘Work Flow’.
 For extending the program to enable importing different data
 The time point can also be set from the menu Frap calc à Set Bleach Point