Density-Profile Processes Describing Biological Signaling Networks: Almost Sure Convergence to Deterministic Trajectories

被引:6
|
作者
Fernandez, Roberto [2 ]
Fontes, Luiz R. [1 ]
Neves, E. Jordao [1 ]
机构
[1] Univ Sao Paulo, BR-05508090 Sao Paulo, Brazil
[2] Univ Rouen, CNRS, UMR 6085, Lab Math Raphael Salem, F-76801 St Etienne, France
基金
巴西圣保罗研究基金会;
关键词
Density-profile processes; Biological signaling networks; Spin-flip dynamics; Non-reversible stochastic dynamics; Thermodynamic limit; Dynamical system; Mean field; DYNAMICS; MODULES; MECHANISMS; PATHWAYS;
D O I
10.1007/s10955-009-9819-9
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We introduce jump processes in R-k, called density-profile processes, to model biological signaling networks. Our modeling setup describes the macroscopic evolution of a finite-size spin-flip model with k types of spins with arbitrary number of internal states interacting through a non-reversible stochastic dynamics. We are mostly interested on the multi-dimensional empirical-magnetization vector in the thermodynamic limit, and prove that, within arbitrary finite time-intervals, its path converges almost surely to a deterministic trajectory determined by a first-order (non-linear) differential equation with explicit bounds on the distance between the stochastic and deterministic trajectories. As parameters of the spin-flip dynamics change, the associated dynamical system may go through bifurcations, associated to phase transitions in the statistical mechanical setting. We present a simple example of spin-flip stochastic model, associated to a synthetic biology model known as repressilator, which leads to a dynamical system with Hopf and pitchfork bifurcations. Depending on the parameter values, the magnetization random path can either converge to a unique stable fixed point, converge to one of a pair of stable fixed points, or asymptotically evolve close to a deterministic orbit in Rk. We also discuss a simple signaling pathway related to cancer research, called p53 module.
引用
收藏
页码:875 / 901
页数:27
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