Quantum mechanics

Context (archaeology)

Biology

Applied mathematics

Expression (computer science)

Steady state (chemistry)

Computer science

Classical mechanics

Statistical physics

Computational biology

Physical chemistry

Paleontology

Physics

Mathematics

Rate equation

Political science

Kinetics

Chemistry

Programming language

Bistability

PLoS Computational Biology

For over a century, the Michaelis–Menten (MM) rate law has been used to describe the rates of enzyme-catalyzed reactions and gene expression. Despite the ubiquity of the MM rate law, it accurately captures the dynamics of underlying biochemical reactions only so long as it is applied under the right condition, namely, that the substrate is in large excess over the enzyme-substrate complex. Unfortunately, in circumstances where its validity condition is not satisfied, especially so in protein interaction networks, the MM rate law has frequently been misused. In this review, we illustrate how inappropriate use of the MM rate law distorts the dynamics of the system, provides mistaken estimates of parameter values, and makes false predictions of dynamical features such as ultrasensitivity, bistability, and oscillations. We describe how these problems can be resolved with a slightly modified form of the MM rate law, based on the total quasi-steady state approximation (tQSSA). Furthermore, we show that the tQSSA can be used for accurate stochastic simulations at a lower computational cost than using the full set of mass-action rate laws. This review describes how to use quasi-steady state approximations in the right context, to prevent drawing erroneous conclusions from in silico simulations.

Misuse of the Michaelis–Menten rate law for protein interaction networks and its remedy