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Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
19/9, lab lecture (mandatory)
20/9, odd groups, lab work (mandatory)
21/9, even groups, lab work (mandatory)
22/9, 12:45-15:30, compilation (mandatory, teacher will sign your lab journal)
23/9, 9:00-11:30, compilation (not mandatory)
1/10, deadline for the lab report
20160919
Lab lecture
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Introduction on enzyme and kinetics Michaelis-Menten kinetics KM, Vmax and kcat Lineweaver-Burk plot Enzyme inhibition, competitive and non-competitive inhibition
Spectrophotometer and Beer-Lambert Law
Lab procedure Lab execution Lab report
Safety in the lab
20160919
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Introduction – Enzyme
ΔG‡ (with enzyme)
ΔG‡ (without enzyme)
Substrate
Product
Transition state, S‡
Free
ene
rgy
Reaction progress
ΔG for the reaction
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Enzymes are biological catalysts characterized by Catalytic efficiency Specificity Regulated activity
Enzyme-catalyzed reactions are affected by Enzyme concentration Substrate concentration Temperature pH Inhibitors Activators
SubstrateEnzyme
Product
Lab lecture - Enzyme Kinetics and Photometry (QC HT16) 20160919
Kinetics is the study of chemical reaction rate (v, stands for velocity)
Enzyme kinetics is the study of enzyme catalyzed reaction
Determination of kinetics parameter measurement of enzyme activity
Introduction – Kinetics
ΔG‡ (with enzyme)
ΔG‡ (without enzyme)
Substrate
Product
Transition state, S‡
Free
ene
rgy
Reaction progress
ΔG for the reaction
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Introduction – Order of reactoin
·
S k P
Reactio
n rate, v
Substrate concentration [S]
Zero order reaction
First order reaction
k
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First order reaction (v k · S ) Reaction rate is proportional to the substrate’s concentration. This is
true when the substrate concentration is low during the reaction, and the substrate is the determine factor for the reaction rate.
Zero order reaction (v k · S ) The reaction rate is independent of the substrate concentration. This is
true when the substrate concentration is much higher than the enzyme concentration during the reaction, and the enzyme is the determine factor for the reaction rate.
Michaelis-Menten kinetics
To understand how enzyme functions, we need a kinetic description of their activity.
The reaction rate rises linearly as substrate concentration increases (first order reaction) and then begins to level off and approach a maximum at higher substrate concentration (zero order reaction)
For many enzymes, the reaction rate V0 is defined as the number of moles of product formed per unit time when [P] is low, that is at times close to zero (hence, V0)
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Reactio
n rate, v
Substrate concentration [S]
First order reaction
Zero order reaction
Reactio
n rate, v
Time
[S1]
[S2]
[S3]
[S4]V0
V0
V0
V0
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Michaelis-Menten kinetics
At very low substrate concentration ( ≪ → ) : The reaction rate is directly proportional to the substrate concentration
At very high substrate concentration ( ≫ → ): The reaction rate is maximal, independent of substrate concentration.
When KM is equal to the substrate concentration ( → ): KM is equal to the substrate concentration at which the reaction rate is half
its maxim value
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Reaction rate
Substrate concentration [S]
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⇌ ⇀
Michaelis-Menten kinetics
Michaelis constant (Km) KM has the units of concentration KM is a physical constant characterizing a certain enzyme in term of specificity, affinity, etc.
KM is independent of either [E] or [S] KM is an inverse measure of the substrate's affinity for the enzyme
A bigger KM indicates lower affinity.
Lab lecture - Enzyme Kinetics and Photometry (QC HT16) 20160919
Velo
city
..........................
..........................
Lineweaver-Burk plot
Vmax is difficult to estimate because the initial reaction rate approaching Vmax asymptotically withincreasing substrate concentration. In addition, the high concentration of substrate often inhibitsreaction rate. To solve this problem, Lineweaver and Burk (1934) had inverted the Michaelis-Menten equation, which is referred as Lineweaver-Burk plot (or Double reciprocal plot):
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
·
In this equation, 1/V and 1/[S] arevariables, while KM/Vmax and 1/Vmax areconstants. This can be plotted as alinear equation (y = ax + b).Specifically, 1/v is y, 1/[S] is x, KM/Vmaxis a (slope) and 1/Vmax is b (y-intercept). We can accurately calculateKM and Vmax value from a Lineweaver-Burk plot.
y = ax + b
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Nonlinear regression
Indeed, KM and Vmax values can be calculateddirectly from the Michaelis-Menten equationthrough nonlinear regression.
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
y = ax/(b+x)
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http://www.colby.edu/chemistry/PChem/scripts/lsfitpl.html(in short: http://bit.ly/1re1XU4)
Input the data pairs (V and [S])
Choose fit function: ax/(b+x)
Leave Parameter guesses as it is.
Choose Convergence Mode: Damped or Strongly damped
Click Fit or Fit & Plot (Java needed for plotting)
Nonlinear regression
Indeed, KM and Vmax values can be calculateddirectly from the Michaelis-Menten equationthrough nonlinear regression.
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
y = ax/(b+x)
20160919
http://www.colby.edu/chemistry/PChem/scripts/lsfitpl.html(in short: http://bit.ly/1re1XU4)
Input the data pairs (V and [S])
Choose fit function: ax/(b+x)
Leave Parameter guesses as it is.
Choose Convergence Mode: Damped or Strongly damped
Click Fit or Fit & Plot (Java needed for plotting)
Inhibition of enzyme activity
Competitive inhibition
Noncompetitive inhibition
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Enzyme Enzyme
Competitive inhibitor
Enzyme
Noncompetitive inhibitor
Substrate
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Inhibition of enzyme activity Competitive inhibition
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Enzyme
Competitive inhibitor
No inhibitor
Competitive inhibitorNo inhibitor
+ Competitive inhibitor
Vmax is not affected KM is increased
+I
EI
E + S ES E + P
ki S
I
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Inhibition of enzyme activity Noncompetitive inhibition
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
No inhibitor
Noncompetitive inhibitor
S IE + I ES E + P
kiS
EI EIS ×
No inhibitor
+ Noncompetitive inhibitor
Enzyme
Noncompetitive inhibitor
Vmax is decreasedKM is not affected
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Inhibition of enzyme activity
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
No inhibitor
Mix inhibition
Vmax is decreasedKM is not affected
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No inhibitor
Competitive inhibitor
No inhibitor
Noncompetitive inhibitor
Vmax is not affected KM is increased
Vmax is decreasedKM is increased
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Photometry - Spectrophotometer
How to measure the chemical reactions rate Different molecules have different
absorption Some molecules (e.g. proteins) have
several absorbance peaks during the wave scan
Spectrophotometer
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Light source Filter Sample Detector Readout
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Photometry - Beer-Lambert law
Beer-Lambert law is a mathematical means of expressing how light is absorbed bymatter. The law states that the amount of light emerging from a sample isdiminished by three physical phenomena:
The concentration of absorbing sample in its pathway (C, in unit of molarity, M)
The distance the light travels through the sample (ℓ, in units of centimeters, cm)
The probability that the light of that particular wavelength will be absorbed bythe material, also known as molar absorption (or extinction) coefficient (ε), inunits that are reciprocals of molarity and distance in centimeters, M-1cm-1)
T: 0 - 1A: ∞ - 0
Due to technical limitation, the best readingrange of spectrophotometer is normallyfrom 0.1 – 1, thus:
o If A is too high, dilute the sampleo If A is too low, concentrate the sample
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Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab training
Enzyme: Alkaline Phosphatase (ALP) Remove phosphate groups from many types of molecules. Function as a dimer, and take effect under alkaline conditions Made in liver, bone, and other tissues. It can be measured in a routine blood test. Abnormally high serum
levels of ALP may indicate bone, liver disease, etc.
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Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab training – Outline
Determine the following parameters of alkaline phosphataseusing p-nitro-phenyl-phosphate (NPP) as substrate Optimal pH KM
Vmax
Inhibition
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p-Nitro-Phenyl-Phosphate (NPP)
p-Nitrophenol
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Determine the maximal absorbance (λmax) for p-nitrophenol
Set wavelength scan in the range of 350 – 500 nm
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Calculating molar absorption coefficient (ε) using Beer-Lambert law
· · ·
Lab training – Maximal absorbance
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab training – Incubation time
The effect of incubation time on the amount of product formed
Incubation at 40⁰C water bath Incubation time (9 different time from 0.5-20 min) Measure absorbance within 15 min at the end of the reaction Plot: amount of product formed (y-axis) against time (x-axis)
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dH2ONFF
Buffer with pH 9.5
Testing tubes (× 9)Add enzyme
Blank tubes (× 9)Add dH2O
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab training – Optimal pH
The effect of pH on the reaction rate (v)
Incubation at 40⁰C water bath Incubation time: 10 min Measure absorbance within 15 min at the end of the reaction Plot: amount of product formed (y-axis) against time (x-axis)
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dH2ONFF
Buffer with differnt pH
Testing tubes (× 9)Add enzyme
Blank tubes (× 9)Add dH2O
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab training – KM, Vmax, Inhibition
Determine the KM and Vmax value for alkaline phosphatase, and the inhibition type of the inhibitor provided
Incubation at 40⁰C water bath Incubation time: 10 min Measure absorbance within 15 min at the end of the reaction Michaelis-Menten plot: Reaction rate (y-axis) against [S] (a-axis) Lineweaver-Burk plot: 1/V (y-axis) against 1/[S] (a-axis) Determine KM, Vmax, and inhibition type
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Each series contains 6 tubes with different substrate concentration [S]
a. With enzyme onlyb. With enzyme and 1st inhibitor (0.5 mM phosphate solution)c. With enzyme and 2nd inhibitor (1 mM phosphate solution)d. Blank (with neither enzyme nor the inhibitor)
a b c d
Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab training – Case study (ADH)
KM determination for alcohol dehydrogenase
Determine KM, Vmax, of alcohol dehydrogenase using eithermethanol or ethanol as substrate from the values in the labcompendium.
Determine inhibition type of ethanol on ADH when usingmethanol as substrate.
Calculate the blood alcohol content (BAC) in the patientundergone ethanol treatment.
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Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab journal and reports
Write journal carefully, which should be approved and countersigned by your teaching assistant.
A written lab report per group is needed Brief introduction and aim Brief description of the execution of the lab work Results including all the raw data, calculations including the
equation, and all the plots. Don’t forget to specify units in calculations and plots Brief conclusions and discussion Answer all the questions in the compendium.
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Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Lab safty
Lab coat, goggles, gloves No eating or drinking in the lab Prevent accidents
Be well prepared Work calmly
When you leave the lab Wash hands Remove lab coat
Use your judgment Ask teaching assistant
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Lab lecture - Enzyme Kinetics and Photometry (QC HT16)
Question?
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