mini-course: molecular systems biologyglue.jjj.sun.ac.za/jjj/minicourse/lecture2_2020.pdf ·...
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Mini-course: Molecular Systems Biology
Prof Jacky Snoep (lectures), Dr Dawie van Niekerk (tutorials),Johann Rohwer (practical and data analysis)
February – March 2020
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First Lecture: Chemical Kinetics
• order of reaction vs molecularity
• direction of reaction, ∆G
• mass action kinetics
• mass action ratio
• disequilibrium ratio, Γ/Keq
• ∆G0, relation to Keq
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Second Lecture: Enzyme Kinetics
• derivations of reversible Michaelis-Menten kinetic equation using equilibrium binding model
• Haldane relation
• characteristics of enzyme kinetics
• types of inhibition
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Michaelis-Menten kinetics
Michaelis Menten equation describes enzyme activity in absence of product:
This equation is often used for the description of initial rates of in vitro enzyme activities, but generally does not work for coupled reactions due to the presence of product in such systems.
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Deriving a kinetic rate equation: equilibrium binding approach
1. Write down mechanism2. Write down conservation equation for enzyme
species3. Assume equilibrium binding of substrates and
products4. Express bound enzyme species in terms of free
enzyme, [S] and [P], and their dissociation constants
5. Work out fractional saturation with S and P6. Solve v = kf[ES] – kr[EP]
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Derivation of irreversible Michaelis-Menten equation: equilibrium binding
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Deriving a kinetic rate equation: steady-state approximation
1. Write down mechanism2. Write down conservation equation for enzyme
species3. Assume steady state for bound enzyme species4. Express bound enzyme species in terms of free
enzyme, [S] and [P], and the rate constants of the mechanism
5. Work out fractional saturation with S and P6. Solve v = kf[ES] – kr[EP]
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steady state approximation
Derivation of irreversible Michaelis-Menten equation: steady-state approximation
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Reversible form of the Michaelis-Menten equation
Equilibrium binding assumption
Dissociation constants KS and KP Conservation relation
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Fraction of enzyme in ES form, YES:
Fraction of enzyme in EP form, YEP:
Reversible form of the Michaelis-Menten equation (2)
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Reversible form of the Michaelis-Menten equation (3)
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Reversible Michaelis-Menten: Steady-state approximation
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Reversible Michaelis-Menten: Steady-state approximation (2)
𝑉 +𝑀𝐴𝑋 =
𝑛𝑢𝑚1
𝑐𝑜𝑛𝑠𝑡
𝑉 −𝑀𝐴𝑋 =
𝑛𝑢𝑚2
𝑐𝑜𝑛𝑠𝑡
𝐾𝑀𝑆 =𝑐𝑜𝑛𝑠𝑡𝑐𝑜𝑒𝑓𝑠
𝐾𝑀𝑃 =𝑐𝑜𝑛𝑠𝑡𝑐𝑜𝑒𝑓𝑝
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Haldane relation
at equilibrium v = 0:
leading to the Haldane relation (not limited to eq. state)
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Reversible Michaelis-Menten: second form (in terms of Keq)
substituting Vmr with the Haldane relation:
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Try it yourself!Derive the rate equation for an enzyme acted on by an inhibitor I, with the following mechanism:
ESI
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Multiple subunits: Cooperativity
In enzymes consisting of more than one subunit, the binding of substrate to a subunit can influence the binding of substrate to the other subunit(s). This effect is called cooperativity and can be positive or negative.
Rate equations for enzymes showing cooperativity, typically have the (s/Ks) term taken to a power h (h>1, positive; h<1, negative cooperativity). The well known sigmoidal saturation curve is typical for positive cooperativity.
Hill-equation:
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Other binding site: allostery
Some enzymes have other binding sites in addition to the the active site. Binding to such sites can effect the activity of the enzyme. This effect is called allostery, the effect can be positive or negative.
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Reversible Hill equation
A relatively simple kinetic equation that can accommodate cooperativity and allosteric effectors is the reversible Hill equation:
with X as allosteric effector; if α<1 then X is an inhibitor, if α>1 an activator.
Reduce the above equation by substituting: α=1, h=1, p=0.
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Analysis of experimental data
For an enzyme catalyzed, chemical reaction, A B, the following initial rates were obtained
(a and b given at t = 0):
Calculate:• Vmf
• Vmr
• Ka
• Kb
• Keq
v a b(mM/s) (mM) (mM)
9.9 10 07.86 10 59.8 5 06.01 10 10-30.3 0 10-32.68 0 50
Assume a random order mechanism and rapid equilibrium binding of substrate and product.