A simple generalized equation for the analysis of multiple inhibitions of Michaelis-Menten kinetic systems
- PMID: 893418
A simple generalized equation for the analysis of multiple inhibitions of Michaelis-Menten kinetic systems
Abstract
The summation of the effects of two or more reversible inhibitors of various types on the initial velocity of enzyme systems obeying Michaelis-Menten kinetics is described by the the general relation: (formula: see text) wherein v1,2,3...n is the velocity of reaction in the simultaneous presence of n inhibitors, vi is the velocity observed in the presence of each individual inhibitor, and v0 is the velocity in the absence of inhibition. The derivation is based on the assumption that each enzyme species can combine with no more than one of the inhibitors (i.e. the inhibitors are mutually exclusive). The above relationship holds irrespective of the number of inhibitors, the type of inhibition (competitive, noncompetitive, or uncompetitive), or the kinetic mechanism (sequential or ping-pong) of the enzyme reaction under consideration. Deviations from this equality define synergism or antagonism of inhibitors depending on whether the value of the left side of the above equation is greater or smaller than the right, respectively. Knowledge of the kinetic constants for substrates and inhibitors is not required. If two or more inhibitors act independently (i.e. are not mutually exclusive), their combined effects are necessarily synergistic. Under certain circumstances, described in the text, mutually nonexclusive inhibitors obey the fractional velocity product relationship: v1,2,3...n/v0 = (v1/v0) x (v2/v0) x (v3/v0)...(vn/v0).
Similar articles
-
The interaction between full and partial inhibitors acting on a single enzyme. A theoretical analysis.Mol Pharmacol. 1983 Jul;24(1):30-41. Mol Pharmacol. 1983. PMID: 6865924
-
A new plot for multiple enzyme inhibition.Biochem Int. 1983 Aug;7(2):247-53. Biochem Int. 1983. PMID: 6383391
-
Kinetic study of an enzyme-catalysed reaction in the presence of novel irreversible-type inhibitors that react with the product of enzymatic catalysis.Bull Math Biol. 1995 Jan;57(1):157-68. doi: 10.1007/BF02458321. Bull Math Biol. 1995. PMID: 7833851
-
Mechanistic and kinetic studies of inhibition of enzymes.Cell Biochem Biophys. 2000;33(3):217-25. doi: 10.1385/cbb:33:3:217. Cell Biochem Biophys. 2000. PMID: 11325042 Review.
-
A guide to the Michaelis-Menten equation: steady state and beyond.FEBS J. 2022 Oct;289(20):6086-6098. doi: 10.1111/febs.16124. Epub 2021 Jul 31. FEBS J. 2022. PMID: 34270860 Review.
Cited by
-
Characterization and mitigation of gene expression burden in mammalian cells.Nat Commun. 2020 Sep 15;11(1):4641. doi: 10.1038/s41467-020-18392-x. Nat Commun. 2020. PMID: 32934213 Free PMC article.
-
Linker for activation of T-cell family member2 (LAT2) a lipid raft adaptor protein for AKT signaling, is an early mediator of alkylphospholipid anti-leukemic activity.Mol Cell Proteomics. 2012 Dec;11(12):1898-912. doi: 10.1074/mcp.M112.019661. Epub 2012 Sep 22. Mol Cell Proteomics. 2012. PMID: 23001822 Free PMC article.
-
Pre-clinical evaluation of antiproteases as potential candidates for HIV-1 pre-exposure prophylaxis.Front Reprod Health. 2022 Nov 21;4:998913. doi: 10.3389/frph.2022.998913. eCollection 2022. Front Reprod Health. 2022. PMID: 36478892 Free PMC article.
-
Chidamide epigenetically represses autophagy and exerts cooperative antimyeloma activity with bortezomib.Cell Death Dis. 2020 Apr 27;11(4):297. doi: 10.1038/s41419-020-2414-3. Cell Death Dis. 2020. PMID: 32341332 Free PMC article.
-
Effect of Supplementation of Tanshinone IIA and Sodium Tanshinone IIA Sulfonate on the Anticancer Effect of Epirubicin: An In Vitro Study.Evid Based Complement Alternat Med. 2011;2011:841564. doi: 10.1155/2011/841564. Epub 2011 May 24. Evid Based Complement Alternat Med. 2011. PMID: 21716682 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources