| Literature DB >> 30615881 |
Justin Eilertsen1, Wylie Stroberg1, Santiago Schnell2.
Abstract
Scaling analysis exploiting timescale separation has been one of the most important techniques in the quantitative analysis of nonlinear dynamical systems in mathematical and theoretical biology. In the case of enzyme catalyzed reactions, it is often overlooked that the characteristic timescales used for the scaling the rate equations are not ideal for determining when concentrations and reaction rates reach their maximum values. In this work, we first illustrate this point by considering the classic example of the single-enzyme, single-substrate Michaelis-Menten reaction mechanism. We then extend this analysis to a more complicated reaction mechanism, the auxiliary enzyme reaction, in which a substrate is converted to product in two sequential enzyme-catalyzed reactions. In this case, depending on the ordering of the relevant timescales, several dynamic regimes can emerge. In addition to the characteristic timescales for these regimes, we derive matching timescales that determine (approximately) when the transitions from transient to quasi-steady-state kinetics occurs. The approach presented here is applicable to a wide range of singular perturbation problems in nonlinear dynamical systems.Entities:
Keywords: Chemical kinetics; Enzyme kinetics; Nonlinear dynamical systems; Perturbation methods; Slow and fast dynamics; Timescales
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Year: 2019 PMID: 30615881 PMCID: PMC6612542 DOI: 10.1016/j.jtbi.2019.01.005
Source DB: PubMed Journal: J Theor Biol ISSN: 0022-5193 Impact factor: 2.691