Overview of Ligand Binding Module
Features in Ligand Binding Module
Report Generation in Ligand Binding Module
Graphs in Ligand Binding Module
Ligand Binding Module Equations
Ligard Binding Module Requirement
The Enzyme Kinetics Module is a SigmaPlot add-on that guides you through data entry, analysis and graphing of your enzyme kinetics data. Select the study type in the customized Data Entry Wizard, choose from 56 built-in equations, then discover the best fit to characterize the reaction mechanism. Automatically display a series of graphs to quickly determine the type of inhibition. The module continues SigmaPlot's tradition of award-winning interface, ease-of-use and intelligent wizards to guide you through your analysis.
The Electrophysiology Module is an add-on to SigmaPlot that allows you to directly import your acquired data into SigmaPlot without the need for an additional data acquisition program. The module saves you the time and effort of manually entering data into SigmaPlot so you can start your analysis and graphing right away. Use the easy point-and-click interface to import your data from commonly used file formats including Axon Instruments ABF files, Bruxton Corporation's Acquire format and HEKA electronik's Pulse format. The file formats appear as a convenient drop down list in SigmaPlot.
Automatically fit your radioligand and dose response studies for multiple compounds with replicate data. Choose from over 10 built-in equations, create a new equation or modify and existing equation to gain insight on the number of binding sites, and their affinity and accessibility for various drugs. Automatically generate a plot of mean response versus concentration and include the best-fit lines for each compound.
EQUATIONS of SIGMAPLOT LIGAND BINDING MODULES


  • One Site Saturation



This equation is used to fit specific binding data (y) as a function of ligand concentration (x).



  • Variable Range Definition Units
    x >= 0 concentration of free ligand* concentration, M
    y >= 0 specific binding (=total - nonspecific) cpm, sites/cell, fmol of receptor/mg of tissue
    Bmax >0 maximum number of binding sites same as y
    Kd >0 concentration of ligand to reach half maximal binding concentration


  • Two Site Saturation



This equation accounts for two receptor binding sites with two different affinities.



Variable Range Definition Units
x >= 0 concentration of free ligand concentration, M
y >= 0 specific binding (=total - nonspecific) cpm, sites/cell, fmol of receptor/mg of tissue
Bmax1 >0 maximum number of binding sites for receptor 1 same as y
Bmax2 >0 maximum number of binding sites for receptor 2 same as y
Kd1 >0 equilibrium dissociation constant for receptor 1 concentration
Kd2 >0 equilibrium dissociation constant for receptor 2 concentration



  • One Site Saturation + Nonspecific



This equation is used to fit total binding concentration (y) as a function of ligand concentration (x). The extra parameter (from the one site saturation equation) N accounts for the nonspecific binding. You will need additional data points to get good estimates of the three parameters.




Variable Range Definition Units
x >= 0 concentration of free ligand concentration, M
y >= 0 total binding cpm, sites/cell, fmol of receptor/mg of tissue
Bmax1 >0 maximum number of binding sites for receptor 1 same as y
Bmax2 >0 maximum number of binding sites for receptor 2 same as y
Kd1 >0 equilibrium dissociation constant for receptor 1 concentration
Kd2 >0 equilibrium dissociation constant for receptor 2 concentration



  • Two Site Saturation + Nonspecific



This equation is used to fit total binding concentration (y) as a function of the ligand concentration (x) when the data supports the existence of two receptor binding sites. This equation has five parameters and will require a considerable number of data points to accurately estimate these parameters.




Variable Range Definition Units
x >= 0 concentration of free ligand concentration, M
y >= 0 total binding cpm, sites/cell, fmol of receptor/mg of tissue
Bmax1 >0 maximum number of binding sites for receptor 1 same as y
Bmax2 >0 maximum number of binding sites for receptor 2 same as y
Kd1 >0 equilibrium dissociation constant for receptor 1 concentration
Kd2 >0 equilibrium dissociation constant for receptor 2 concentration
N >0 slope of nonspecific binding line y units / x units


  • Sigmoidal Dose Response



This equation describes a typical dose-response relationship. The drug data x is entered in logarithmic form. The y variable is the response. EC50 is the drug concentration for y halfway between min and max.



Variable Range Definition Units
x >0 log concentration of drug log concentration, log(M)
y >= 0 response response units
min >0 minimum response plateau same as y
max >0 minimum response plateau same as y
LogEC50 >0 log of EC50 or IC50 log concentration

 

  • Sigmoidal Dose Response (Variable Slope)



This equation describes a typical dose-response relationship but includes an additional parameter, Hillslope, which characterizes the slope of the curve at its midpoint. The drug data x is entered in logarithmic form. This equation is identical to the sigmoidal dose response curve when Hillslope = 1.0. It is also identical to the four-parameter logistic function except the slope parameters have opposite sign.



Variable Range Definition Units
x >= 0 response response units
y >0 minimum response plateau same as y
min >0 minimum response plateau same as y
max >0 log of EC50 or IC50 log concentration
Hillslope all related to slope of curve. When > 0 curve increases with x. unitless

 

  • One Site Competition



In a competition study a ligand is added which competes for another ligand (both ligands may be the same) already attached to a receptor. As ligand is added the amount of existing ligand bound decreases. The one site competition equation characterizes this decrease with added ligand. The drug data x is entered in logarithmic form. This equation is identical to the sigmoidal dose-response equation except for the sign change in the exponent (the sigmoidal dose-response equation increases with x whereas the one site competition decreases).



Variable Range Definition Units
x >0 log concentration of cold liganda log concentration, log(M)
y >= 0 total or specific bindingb,c cpm, % specific binding, sites/cell, fmol of receptor/mg of tissue
min >0 nonspecific binding same as y
max >0 maximum binding in absence of cold ligand same as y
LogEC50 >0 log of EC50 or IC50 log concentration

a .enter x values in log units so that confidence limits for EC50 are > 0.

b .if use total then min is the nonspecific binding

c .if use % specific then the user might want to constrain min to 0 and max to 100

  • Two Site Competition



This equation is used for competition studies where the ligand binds to two receptors. The drug data x is entered in logarithmic form.



Variable Range Definition Units
x >0 log concentration of cold ligand log concentration, log(M)
y >= 0 total or specific binding cpm, % specific binding, sites/cell, mol of receptor/mg of tissue
min >0 nonspecific binding same as y
max >0 maximum binding in absence of cold ligand same as y
F1 >0 Fraction of receptors with affinity logEC501 unitless
LogEC501 >0 log of EC501 or IC501 log concentration
LogEC5 >0   log concentration


  • Four-Parameter Logistic Function



This function is most frequently used for standard curves, radioimmunoassays and dose-response curves. It is included here only for the standard A, B, C, D parameter terminology that is commonly used in these fields. The drug data x is entered in logarithmic form. Except for a sign difference in the slope parameters it is exactly the same as the sigmoidal dose-response (variable slope) equation.



Variable Range Definition Units
x >0 log concentration of drug, dose log concentration, log(M)
y      
D >0 maximum response plateau same as y
A >0 maximum response plateau same as y
logC >0 log of EC50 or IC50 log concentration
B all related to slope of curve. When > 0 curve increases with x. unitless


  • Four-Parameter Logistic Function (Linear)



This is identical to the four-parameter logistic equation except that the linear form of dose concentration (x data) is entered into the worksheet. This equation and the four-parameter logistic equation will yield exactly the same numerical curve fit results. The only reason to use this equation is if you want a graph with a linear X-axis scale. Fitting the four-parameter logistic equation using log(x) data and then changing the X-axis scale to linear will result in a fit line with poor resolution. Using this equation solves this problem.



Variable Range Definition Units
x >0 concentration of drug, dose log concentration, log(M)
y >= 0 response response units
D >0 minimum response plateau  
A >0 minimum response plateau  
logC >0 log of EC50 or IC50 log concentration
B all related to slope of curve. When > 0 curve increases with x. unitless
  • One Site Competion, max=100

  • Fit built-in equations, modify or enter your own

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