1 Exercise 15 Drug binding and investigation of the Michaelis Menten equation; pitfall of methods of...
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![Page 1: 1 Exercise 15 Drug binding and investigation of the Michaelis Menten equation; pitfall of methods of linearisation.](https://reader035.fdocuments.us/reader035/viewer/2022070411/56649f535503460f94c78383/html5/thumbnails/1.jpg)
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Exercise 15Drug binding and investigation
of the Michaelis Menten equation; pitfall of methods of
linearisation
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The Michaelis Menten equation
SKm
SVVelocity
]max[
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Equation relating bound vs Free drug concentration
• where Bound is the bound drug concentration,• Bmax the maximal binding capacity of the transport
protein(s) • Kd the steady state dissociation constant.
– Kd is the free concentration of the drug for which the bound concentration is equal to Bmax/2.
– The inverse of Kd is Ka, the steady-state constant of affinity.• The unit of ka is the inverse of concentration. For example a Ka equal
to 5X109 M means that to obtain half the saturation of Bmax, one mole of ligand should be diluted in a volume of 5X109 L.
FreeKd
FreeBBound
max
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Free fraction vs free concentration
• In blood, a drug (ligand) coexists under two forms: bound [B] and unbound.
• The unbound drug is also called free [Free].• The proportion (fraction) of drug that is free depends on
the specific drug affinity for plasma proteins.– This proportion is noted fu (from 0 to 1 or 0 to 100%) with u
meaning unbound
][
][
Total
Freefu
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Free vs total concentrations
• In PK, the most commonly used analytical methods measure the total (plasma) drug concentrations i.e. [Total=B+Free].
• As generally only the unbound part of a drug is available at the target site of action including pathogens, the assessment of blood and plasma protein binding is critical to evaluate the in vivo free concentrations of drug i.e. [Free].
![Page 6: 1 Exercise 15 Drug binding and investigation of the Michaelis Menten equation; pitfall of methods of linearisation.](https://reader035.fdocuments.us/reader035/viewer/2022070411/56649f535503460f94c78383/html5/thumbnails/6.jpg)
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Computation of the Free concentration from total concentration
ionconcentratplasmaTotalfuionconcentratplasmaFree
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Determination of fu
KdB
Kdfu
max
FreeKd
FreeBBound
max
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Determination of Bmax & Kd
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Determination of fu
1
2
Chamber
Chamberfu
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Determination of fu
• A more advanced protocol consists in repeating this kind of experiment but with very different values of drug concentrations in order to exhibit a possible saturation of the tested proteins.
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Data to analyse
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Plot of data
Linear portion
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Equation to fit
• Where NS is the proportionality costant for the Non Saturable binding
FreeNSFreeKd
FreeBFreeTotal
max
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Estimation of Bmax, Kd and NS using Non-Linear regression
• MODEL• remark ******************************************************• remark Developer: PL Toutain• remark Model Date: 03-29-2011• remark Model Version: 1.0• remark ******************************************************• remark• remark - define model-specific commands • COMMANDS • NSECO 3• NFUNCTIONS 1• NPARAMETERS 3• PNAMES 'Bmax', 'Kd', 'NS'• SNAMES 'fu5', 'fu100','fu1000'• END• remark - define temporary variables• TEMPORARY • Free=x• END • remark - define algebraic functions• FUNCTION 1• F= Free+(Bmax*Free)/(Kd+Free)+NS*Free• END• SECO• remark: free fraction for free=5 or 100 ng/ml• fu5=5/(5+(5*Bmax)/(kd+5)+NS*5)*100• fu100=100/(100+(100*Bmax)/(kd+100)+NS*100)*100• fu1000=1000/(1000+(100*Bmax)/(kd+1000)+NS*1000)*100• END• • remark - define any secondary parameters• remark - end of model• EOM
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The command block
• COMMANDS
• NSECO 3
• NFUNCTIONS 1
• NPARAMETERS 3
• PNAMES 'Bmax', 'Kd', 'NS'
• SNAMES 'fu5', 'fu100','fu1000'
• END
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The temporary block
• TEMPORARY
• Free=x
• END
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The function block
• FUNCTION 1• F= Free+(Bmax*Free)/(Kd+Free)+NS*Free• END
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The SECONDARY block
• SECO• remark: free fraction for free=5 or 100 ng/ml• fu5=5/(5+(5*Bmax)/(kd+5)+NS*5)*100• fu100=100/(100+(100*Bmax)/
(kd+100)+NS*100)*100•
fu1000=1000/(1000+(100*Bmax)/(kd+1000)+NS*1000)*100
• END
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Results
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Linearization of the MM equation
• Before nonlinear regression programs were available, scientists transformed data into a linear form, and then analyzed the data by linear regression. There are numerous methods to linearize binding data; the two most popular are the methods of Lineweaver-Burke and the Scatchard/Rosenthal plot.
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Linearization of the MM equation
• The Lineweaver Burke transformation
max
11
maxmax][
1
BFreeB
Kd
FreeB
FreeKd
B
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The Lineweaver Burke transformation
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Linear regression analysis of binding data
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Estimate parameters after transformation
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Pitfall of the linear regression analysis
• Now repeat your estimation of these two parameters (Bmax, Ka) by linear and non-linear regression but after altering a single value (replace the first value B=61.7 by B=50).