In this thesis we study stochastic modeling and simulation methods for biochemical systems. The thesis is focused on systems with multi-state and multi-scale features and divided into two parts. In the first part, we propose new algorithms that improve existing multi-state simulation methods. We first compare the well known Gillespie\\\'s stochastic simulation algorithm (SSA) with the StochSim, an agent-based simulation method. Based on the analysis, we propose a hybrid method that possesses the advantages of both methods. Then we propose two new methods that extend the Network-Free Algorithm (NFA) for rule-based models. Numerical results are provided to show the performance improvement by our new methods. In the second part, we investigate two simulation schemes for the multi-scale feature: Haseltine and Rawlings\\\' hybrid method and the quasi-steady-state stochastic simulation method. We first propose an efficient partitioning strategy for the hybrid method and an efficient way of building stochastic cell cycle models with this new partitioning strategy. Then, to understand conditions where the two simulation methods can be applied, we develop a way to estimate the relaxation time of the fast sub-network, and compare it with the firing interval of the slow sub-network. Our analysis are verified by numerical experiments on different realistic biochemical models. / Ph. D.

Gillespie's stochastic simulation algorithm (SSA) has been a conventional method for stochastic modeling and simulation of biochemical systems. However, its population-based scheme faces the challenge from multi-state situations in many biochemical models. To tackle this problem, Morton-Firth and Bray's stochastic simulator (StochSim) was proposed with a particle-based scheme. The thesis first provides a detailed comparison between these two methods, and then proposes improvements on StochSim and a hybrid method to combine the advantages of the two methods. Analysis and numerical experiment results demonstrate that the hybrid method exhibits extraordinary performance for systems with both the multi-state feature and a high total population. In order to deal with the combinatorial complexity caused by the multi-state situation, the rules-based modeling was proposed by Hlavacek's group and the particle-based Network-Free Algorithm (NFA) has been used for its simulation. In this thesis, we improve the NFA so that it has both the population-based and particle-based features. We also propose a population-based method for simulation of the rule-based models. The bacterial chemotaxis model has served as a good biological example involving multi-state species. We implemented different simulation methods on this model. Then we constructed a graphical interface and compared the behaviors of the bacterium under different mechanisms, including simplified mathematical models and chemically reacting networks which are simulated stochastically. / Master of Science