Ganguly Arnab, Petrov Tatjana, Koeppl Heinz
Department of Mathematics, University of Louisville, 231 Natural Sciences Building, Louisville, KY, USA,
J Math Biol. 2014 Sep;69(3):767-97. doi: 10.1007/s00285-013-0738-7. Epub 2013 Nov 20.
We consider a continuous-time Markov chain (CTMC) whose state space is partitioned into aggregates, and each aggregate is assigned a probability measure. A sufficient condition for defining a CTMC over the aggregates is presented as a variant of weak lumpability, which also characterizes that the measure over the original process can be recovered from that of the aggregated one. We show how the applicability of de-aggregation depends on the initial distribution. The application section is devoted to illustrate how the developed theory aids in reducing CTMC models of biochemical systems particularly in connection to protein-protein interactions. We assume that the model is written by a biologist in form of site-graph-rewrite rules. Site-graph-rewrite rules compactly express that, often, only a local context of a protein (instead of a full molecular species) needs to be in a certain configuration in order to trigger a reaction event. This observation leads to suitable aggregate Markov chains with smaller state spaces, thereby providing sufficient reduction in computational complexity. This is further exemplified in two case studies: simple unbounded polymerization and early EGFR/insulin crosstalk.
我们考虑一个连续时间马尔可夫链(CTMC),其状态空间被划分为聚合体,并且为每个聚合体分配一个概率测度。作为弱可聚合性的一种变体,给出了在聚合体上定义CTMC的充分条件,这也表明原始过程的测度可以从聚合过程的测度中恢复。我们展示了去聚合的适用性如何依赖于初始分布。应用部分致力于说明所发展的理论如何有助于简化生化系统的CTMC模型,特别是与蛋白质 - 蛋白质相互作用相关的模型。我们假设该模型由生物学家以位点 - 图 - 重写规则的形式编写。位点 - 图 - 重写规则简洁地表达了,通常,为了触发一个反应事件,蛋白质的局部环境(而不是完整的分子物种)处于特定构型就足够了。这一观察结果导致了具有较小状态空间的合适聚合马尔可夫链,从而充分降低了计算复杂度。这在两个案例研究中得到了进一步例证:简单无界聚合和早期表皮生长因子受体(EGFR)/胰岛素串扰。