Division of Systems Biology, Academy of Integrated Science, Virginia Polytechnic Institute and State University, Blacksburg, VA, United States of America.
VT-Center for the Mathematics of Biosystems, Virginia Polytechnic Institute and State University, Blacksburg, VA, United States of America.
PLoS One. 2024 Sep 6;19(9):e0306523. doi: 10.1371/journal.pone.0306523. eCollection 2024.
Considerable effort is required to build mathematical models of large protein regulatory networks. Utilizing computational algorithms that guide model development can significantly streamline the process and enhance the reliability of the resulting models. In this article, we present a perturbation approach for developing data-centric Boolean models of cell cycle regulation. To evaluate networks, we assign a score based on their steady states and the dynamical trajectories corresponding to the initial conditions. Then, perturbation analysis is used to find new networks with lower scores, in which dynamical trajectories traverse through the correct cell cycle path with high frequency. We apply this method to refine Boolean models of cell cycle regulation in budding yeast and mammalian cells.
构建大型蛋白质调控网络的数学模型需要付出相当大的努力。利用指导模型开发的计算算法可以显著简化该过程并提高所得模型的可靠性。在本文中,我们提出了一种用于开发细胞周期调控数据中心布尔模型的摄动方法。为了评估网络,我们根据其稳态和对应于初始条件的动态轨迹为网络分配一个分数。然后,使用摄动分析找到新的网络,其分数更低,动态轨迹以高频遍历正确的细胞周期路径。我们将该方法应用于酿酒酵母和哺乳动物细胞的细胞周期调控布尔模型的优化。