Michaelis–Menten saturation curve for an enzyme reaction showing the relation between the substrate concentration and reaction rate.
In biochemistry, Michaelis–Menten kinetics is one of the best-known models of enzyme kinetics. It is named after German biochemist Leonor Michaelis and Canadian physician Maud Menten. The model takes the form of an equation describing the rate of enzymatic reactions, by relating reaction rate to , the concentration of a substrate S. Its formula is given by
This equation is called Michaelis–Menten equation. Here, represents the maximum rate achieved by the system, at maximum saturation of the substrate concentration. The Michaelis constant is the substrate concentration at which the reaction rate is half of .[1] Biochemical reactions involving a single substrate are often assumed to follow Michaelis–Menten kinetics, without regard to the model's underlying assumptions.
Contents
- 1 Model
- 2 Applications
- 3 Derivation
- 3.1 Equilibrium approximation
- 3.2 Quasi-steady-state approximation
- 3.3 Assumptions and limitations
- 4 Determination of constants
- 5 Role of substrate unbinding
- 6 See also
- 7 References
- 8 Further reading
Model
Change in concentrations over time for enzyme E, substrate S, complex ES and product P
In 1903, French physical chemist Victor Henri found that enzyme reactions were initiated by a bond (more generally, a binding interaction) between the enzyme and the substrate.[2] His work was taken up by German biochemist Leonor Michaelis and Canadian physician Maud Menten, who investigated the kinetics of an enzymatic reaction mechanism, invertase, that catalyzes the hydrolysis of sucrose into glucose and fructose.[3] In 1913, they proposed a mathematical model of the reaction.[4] It involves an enzyme E binding to a substrate S to form a ES complex, which in turn is converted into a product P and the enzyme. This may be represented schematically as
-
where , , and denote the rate constants,[5] and the double arrows between S and ES represent the fact that enzyme-substrate binding is a reversible process.
Under certain assumptions – such as the enzyme concentration being much less than the substrate concentration – the rate of product formation is given by
-
The reaction rate increases with increasing substrate concentration
, asymptotically approaching its maximum rate , attained when all enzyme is bound to substrate. It also follows that
, where
is the initial enzyme concentration. , the turnover number, is the maximum number of substrate molecules converted to product per enzyme molecule per second.
The Michaelis constant is the
at which the reaction rate is at half-maximum,[1] and is an inverse measure of the substrate's affinity for the enzyme—as a small indicates high affinity, meaning that the rate will approach with lower
than those reactions with a larger .[6] The value of is dependent on both the enzyme and the substrate, as well as conditions such as temperature and pH.
The model is used in a variety of biochemical situations other than enzyme-substrate interaction, including antigen-antibody binding, DNA-DNA hybridization, and protein-protein interaction.[6][7] It can be used to characterise a generic biochemical reaction, in the same way that the Langmuir equation can be used to model generic adsorption of biomolecular species.[7] When an empirical equation of this form is applied to microbial growth, it is sometimes called a Monod equation.
Applications
Parameter values vary wildly between enzymes:[8]
| Enzyme |
(M) |
(1/s) |
(1/M*s) |
| Chymotrypsin |
1.5 × 10−2 |
0.14 |
9.3 |
| Pepsin |
3.0 × 10−4 |
0.50 |
1.7 × 103 |
| Tyrosyl-tRNA synthetase |
9.0 × 10−4 |
7.6 |
8.4 × 103 |
| Ribonuclease |
7.9 × 10−3 |
7.9 × 102 |
1.0 × 105 |
| Carbonic anhydrase |
2.6 × 10−2 |
4.0 × 105 |
1.5 × 107 |
| Fumarase |
5.0 × 10−6 |
8.0 × 102 |
1.6 × 108 |
The constant (catalytic efficiency) is a measure of how an enzyme efficiently converts a substrate into product. Diffusion limited enzymes, such as fumarase, work at the theoretical upper limit of 108 – 1010 /M*s, limited by diffusion of substrate into the active site.[9]
Michaelis–Menten kinetics have also been applied to a variety of spheres outside of biochemical reactions,[5] including alveolar clearance of dusts,[10] the richness of species pools,[11] clearance of blood alcohol,[12] the photosynthesis-irradiance relationship, and bacterial phage infection.[13]
Derivation
Applying the law of mass action, which states that the rate of a reaction is proportional to the product of the concentrations of the reactants (i.e.[E][S]), gives a system of four non-linear ordinary differential equations that define the rate of change of reactants with time [14]
![\begin{align}
\frac{d[E]}{dt} &= - k_f [E][S] + k_r [ES] + k_{cat} [ES] \\
\frac{d[S]}{dt} &= - k_f [E][S] + k_r [ES] \\
\frac{d[ES]}{dt} &= k_f [E][S] - k_r [ES] - k_{cat} [ES] \\
\frac{d[P]}{dt} &= k_{cat} [ES].
\end{align}](//upload.wikimedia.org/math/d/9/3/d935b9e73a0e63e6ba1efb5a80baebe1.png)
In this mechanism, the enzyme E is a catalyst, which only facilitates the reaction, so that its total concentration, free plus combined, is a constant. This conservation law can also be observed by adding the first and third equations above.[14][15]
Equilibrium approximation
In their original analysis, Michaelis and Menten assumed that the substrate is in instantaneous chemical equilibrium with the complex, which implies[4][15]
From the enzyme conservation law, we obtain[15]
Combining the two expressions above, gives us
Upon simplification, we get
where is the dissociation constant for the enzyme-substrate complex. Hence the velocity of the reaction – the rate at which P is formed – is[15]
where is the maximum reaction velocity.
Quasi-steady-state approximation
An alternative analysis of the system was undertaken by British botanist G. E. Briggs and British geneticist J. B. S. Haldane in 1925.[16] They assumed that the concentration of the intermediate complex does not change on the time-scale of product formation – known as the quasi-steady-state assumption or pseudo-steady-state-hypothesis. Mathematically, this assumption means . Combining this relationship with the enzyme conservation law, the concentration of complex is[15]
where
is known as the Michaelis constant, where , , and are, respectively, the constants for substrate unbinding, conversion to product, and binding to the enzyme. Hence the velocity of the reaction is[15]
Assumptions and limitations
The first step in the derivation applies the law of mass action, which is reliant on free diffusion. However, in the environment of a living cell where there is a high concentration of proteins, the cytoplasm often behaves more like a gel than a liquid, limiting molecular movements and altering reaction rates.[17] Whilst the law of mass action can be valid in heterogeneous environments,[18] it is more appropriate to model the cytoplasm as a fractal, in order to capture its limited-mobility kinetics.[19]
The resulting reaction rates predicted by the two approaches are similar, with the only difference being that the equilibrium approximation defines the constant as , whilst the quasi-steady-state approximation uses . However, each approach is founded upon a different assumption. The Michaelis–Menten equilibrium analysis is valid if the substrate reaches equilibrium on a much faster time-scale than the product is formed or, more precisely, that [15]
- .
By contrast, the Briggs–Haldane quasi-steady-state analysis is valid if [14][20]
-
.
Thus it holds if the enzyme concentration is much less than the substrate concentration. Even if this is not satisfied, the approximation is valid if is large.
In both the Michaelis–Menten and Briggs–Haldane analyses, the quality of the approximation improves as decreases. However, in model building, Michaelis–Menten kinetics are often invoked without regard to the underlying assumptions.[15]
It is also important to remember that, while irreversibility is a necessary simplification in order to yield a tractable analytic solution, in the general case product formation is not in fact irreversible. The enzyme reaction is more correctly described as
-
.
In general, the assumption of irreversibility is a good one in situations where one of the below is true:
- 1. The concentration of substrate(s) is very much larger than the concentration of products:
-
-
.
This is true under standard in vitro assay conditions, and is true for many in vivo biological reactions, particularly where the product is continually removed by a subsequent reaction.
- 2. The energy released in the reaction is very large, that is
-
In situations where neither of these two conditions hold (that is, the reaction is low energy and a substantial pool of product(s) exists), the Michaelis–Menten equation breaks down, and more complex modelling approaches explicitly taking the forward and reverse reactions into account must be taken to understand the enzyme biology.
Determination of constants
The typical method for determining the constants and involves running a series of enzyme assays at varying substrate concentrations , and measuring the initial reaction rate . 'Initial' here is taken to mean that the reaction rate is measured after a relatively short time period, during which it is assumed that the enzyme-substrate complex has formed, but that the substrate concentration held approximately constant, and so the equilibrium or quasi-steady-state approximation remain valid.[20] By plotting reaction rate against concentration, and using nonlinear regression of the Michaelis–Menten equation, the parameters may be obtained.[21]
Before computing facilities to perform nonlinear regression became available, graphical methods involving linearisation of the equation were used. A number of these were proposed, including the Eadie–Hofstee diagram, Hanes–Woolf plot and Lineweaver–Burk plot; of these, the Hanes–Woolf plot is the most accurate.[21] However, while useful for visualization, all three methods distort the error structure of the data and are inferior to nonlinear regression.[22] Nonetheless, their use can still be found in modern literature.[23]
In 1997 Santiago Schnell and Claudio Mendoza suggested a closed form solution for the time course kinetics analysis of the Michaelis–Menten kinetics based on the solution of the Lambert W function.[24] Namely:
where W is the Lambert W function and
The above equation has been used to estimate and from time course data.[25][26]
Role of substrate unbinding
The Michaelis-Menten equation has been used to predict the rate of product formation in enzymatic reactions for more than a century. Specifically, it states that the rate of an enzymatic reaction will increase as substrate concentration increases, and that increased unbinding of enzyme-substrate complexes will decrease the reaction rate. While the first prediction is well established, the second has never been tested experimentally. To determine whether an increased rate of unbinding does in fact decrease the reaction rate, Shlomi Reuveni et al. mathematically analyzed the effect of enzyme-substrate unbinding on enzymatic reactions at the single-molecule level. According to the study, unbinding of an enzyme from a substrate can reduce the rate of product formation under some conditions, but may also have the opposite effect. As substrate concentrations increase, a tipping point can be reached where an increase in the unbinding rate results in an increase, rather than a decrease, of the reaction rate. The results indicate that enzymatic reactions can behave in ways that violate the classical Michaelis-Menten equation, and that the role of unbinding in enzymatic catalysis still remains to be determined experimentally.[27]
See also
- Enzyme kinetics
- Lineweaver–Burk plot
- Reaction progress kinetic analysis
- Steady state (chemistry)
References
- ^ a b http://www.worthington-biochem.com/introbiochem/substrateconc.html
- ^ Henri, Victor (1903). Lois Générales de l’Action des Diastases. Paris: Hermann. Google books (US only)
- ^ "Victor Henri". Whonamedit?. Retrieved 24 May 2011.
- ^ a b Michaelis, L.; Menten, M.L. (1913). "Die Kinetik der Invertinwirkung". Biochem Z 49: 333–369 (recent translation, and an older partial translation)
- ^ a b Chen, W.W.; Neipel, M.; Sorger, P.K. (2010). "Classic and contemporary approaches to modeling biochemical reactions". Genes Dev 24 (17): 1861–1875. doi:10.1101/gad.1945410. PMC 2932968. PMID 20810646.
- ^ a b Lehninger, A.L.; Nelson, D.L.; Cox, M.M. (2005). Lehninger principles of biochemistry. New York: W.H. Freeman. ISBN 978-0-7167-4339-2.
- ^ a b Chakraborty, S. (23 Dec 2009). Microfluidics and Microfabrication (1 ed.). Springer. ISBN 978-1-4419-1542-9.
- ^ Mathews, C.K.; van Holde, K.E.; Ahern, K.G. (10 Dec 1999). Biochemistry (3 ed.). Prentice Hall. ISBN 978-0-8053-3066-3.
- ^ Stroppolo, M.E.; Falconi, M.; Caccuri, A.M.; Desideri, A. (Sep 2001). "Superefficient enzymes". Cell Mol Life Sci 58 (10): 1451–60. doi:10.1007/PL00000788. PMID 11693526.
- ^ Yu, R.C.; Rappaport, S.M. (1997). "A lung retention model based on Michaelis–Menten-like kinetics". Environ Health Perspect 105 (5): 496–503. doi:10.1289/ehp.97105496. PMC 1469867. PMID 9222134.
- ^ Keating, K.A.; Quinn, J.F. (1998). "Estimating species richness: the Michaelis–Menten model revisited". Oikos 81 (2): 411–416. doi:10.2307/3547060. JSTOR 3547060.
- ^ Jones, A.W. (2010). "Evidence-based survey of the elimination rates of ethanol from blood with applications in forensic casework". Forensic Sci Int 200 (1–3): 1–20. doi:10.1016/j.forsciint.2010.02.021. PMID 20304569.
- ^ Abedon, S.T. (2009). "Kinetics of phage-mediated biocontrol of bacteria". Foodborne Pathog Dis 6 (7): 807–15. doi:10.1089/fpd.2008.0242. PMID 19459758.
- ^ a b c Murray, J.D. (2002). Mathematical Biology: I. An Introduction (3 ed.). Springer. ISBN 978-0-387-95223-9.
- ^ a b c d e f g h Keener, J.; Sneyd, J. (2008). Mathematical Physiology: I: Cellular Physiology (2 ed.). Springer. ISBN 978-0-387-75846-6.
- ^ Briggs, G.E.; Haldane, J.B.S. (1925). "A note on the kinematics of enzyme action". Biochem J 19 (2): 338–339. doi:10.1042/bj0190338. PMC 1259181. PMID 16743508.
- ^ Zhou, H.X.; Rivas, G.; Minton, A.P. (2008). "Macromolecular crowding and confinement: biochemical, biophysical, and potential physiological consequences". Annu Rev Biophys 37 (1): 375–97. doi:10.1146/annurev.biophys.37.032807.125817. PMC 2826134. PMID 18573087.
- ^ Grima, R.; Schnell, S. (Oct 2006). "A systematic investigation of the rate laws valid in intracellular environments". Biophys Chem 124 (1): 1–10. doi:10.1016/j.bpc.2006.04.019. PMID 16781049.
- ^ Schnell, S.; Turner, T.E. (2004). "Reaction kinetics in intracellular environments with macromolecular crowding: simulations and rate laws". Prog Biophys Mol Biol 85 (2–3): 235–60. doi:10.1016/j.pbiomolbio.2004.01.012. PMID 15142746.
- ^ a b Segel, L.A.; Slemrod, M. (1989). "The quasi-steady-state assumption: A case study in perturbation". Thermochim Acta 31 (3): 446–477. doi:10.1137/1031091.
- ^ a b Leskovac, V. (2003). Comprehensive enzyme kinetics. New York: Kluwer Academic/Plenum Pub. ISBN 978-0-306-46712-7.
- ^ Greco, W.R.; Hakala, M.T. (1979). "Evaluation of methods for estimating the dissociation constant of tight binding enzyme inhibitors,". J Biol Chem 254 (23): 12104–12109. PMID 500698.
- ^ Hayakawa, K.; Guo, L.; Terentyeva, E.A.; Li, X.K.; Kimura, H.; Hirano, M.; Yoshikawa, K.; Nagamine, T.; et al. (2006). "Determination of specific activities and kinetic constants of biotinidase and lipoamidase in LEW rat and Lactobacillus casei (Shirota)". J Chromatogr B Analyt Technol Biomed Life Sci 844 (2): 240–50. doi:10.1016/j.jchromb.2006.07.006. PMID 16876490.
- ^ Schnell, S.; Mendoza, C. (1997). "A closed form solution for time-dependent enzyme kinetics". Journal of Theoretical Biology 187 (2): 207–212. doi:10.1006/jtbi.1997.0425.
- ^ Goudar, C. T.; Sonnad, J. R.; Duggleby, R. G. (1999). "Parameter estimation using a direct solution of the integrated Michaelis–Menten equation". Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1429 (2): 377–383. doi:10.1016/s0167-4838(98)00247-7. PMID 9989222.
- ^ Goudar, C. T.; Harris, S. K.; McInerney, M. J.; Suflita, J. M. (2004). "Progress curve analysis for enzyme and microbial kinetic reactions using explicit solutions based on the Lambert W function". Journal of Microbiological Methods 59 (3): 317–326. doi:10.1016/j.mimet.2004.06.013. PMID 15488275.
- ^ Reuveni, Shlomi; Urbakh, Michael; Klafter, Joseph (2014). "Role of Substrate Unbinding in Michaelis-Menten Enzymatic Reactions". Proceedings of the National Academy of Sciences 111 (12): 4391–4396. Bibcode:2014PNAS..111.4391R. doi:10.1073/pnas.1318122111.
Further reading
- Biochemistry/Catalysis at Wikibooks
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Enzymes
|
|
| Activity |
- Active site
- Binding site
- Catalytic triad
- Oxyanion hole
- Enzyme promiscuity
- Catalytically perfect enzyme
- Coenzyme
- Cofactor
- Enzyme catalysis
- Enzyme kinetics
- Lineweaver–Burk plot
- Michaelis–Menten kinetics
|
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| Regulation |
- Allosteric regulation
- Cooperativity
- Enzyme inhibitor
|
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| Classification |
- EC number
- Enzyme superfamily
- Enzyme family
- List of enzymes
|
|
| Types |
- EC1 Oxidoreductases(list)
- EC2 Transferases(list)
- EC3 Hydrolases(list)
- EC4 Lyases(list)
- EC5 Isomerases(list)
- EC6 Ligases(list)
|
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![\begin{align}
\frac{d[E]}{dt} &= - k_f [E][S] + k_r [ES] + k_{cat} [ES] \\
\frac{d[S]}{dt} &= - k_f [E][S] + k_r [ES] \\
\frac{d[ES]}{dt} &= k_f [E][S] - k_r [ES] - k_{cat} [ES] \\
\frac{d[P]}{dt} &= k_{cat} [ES].
\end{align}](http://upload.wikimedia.org/math/d/9/3/d935b9e73a0e63e6ba1efb5a80baebe1.png)