Smith Gregory R, Xie Lu, Schwartz Russell
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania, United States of America.
Joint Carnegie Mellon/University of Pittsburgh Ph.D. Program in Computational Biology, Pittsburgh, Pennsylvania, United States of America.
PLoS One. 2016 May 31;11(5):e0156547. doi: 10.1371/journal.pone.0156547. eCollection 2016.
The environment of a living cell is vastly different from that of an in vitro reaction system, an issue that presents great challenges to the use of in vitro models, or computer simulations based on them, for understanding biochemistry in vivo. Virus capsids make an excellent model system for such questions because they typically have few distinct components, making them amenable to in vitro and modeling studies, yet their assembly can involve complex networks of possible reactions that cannot be resolved in detail by any current experimental technology. We previously fit kinetic simulation parameters to bulk in vitro assembly data to yield a close match between simulated and real data, and then used the simulations to study features of assembly that cannot be monitored experimentally. The present work seeks to project how assembly in these simulations fit to in vitro data would be altered by computationally adding features of the cellular environment to the system, specifically the presence of nucleic acid about which many capsids assemble. The major challenge of such work is computational: simulating fine-scale assembly pathways on the scale and in the parameter domains of real viruses is far too computationally costly to allow for explicit models of nucleic acid interaction. We bypass that limitation by applying analytical models of nucleic acid effects to adjust kinetic rate parameters learned from in vitro data to see how these adjustments, singly or in combination, might affect fine-scale assembly progress. The resulting simulations exhibit surprising behavioral complexity, with distinct effects often acting synergistically to drive efficient assembly and alter pathways relative to the in vitro model. The work demonstrates how computer simulations can help us understand how assembly might differ between the in vitro and in vivo environments and what features of the cellular environment account for these differences.
活细胞的环境与体外反应系统的环境有很大不同,这一问题给使用体外模型或基于这些模型的计算机模拟来理解体内生物化学带来了巨大挑战。病毒衣壳是研究此类问题的极佳模型系统,因为它们通常只有很少的不同组分,便于进行体外和建模研究,然而其组装过程可能涉及复杂的反应网络,目前任何实验技术都无法详细解析这些反应。我们之前根据体外组装的大量数据拟合动力学模拟参数,以使模拟数据与实际数据紧密匹配,然后利用这些模拟来研究无法通过实验监测的组装特征。目前的工作旨在通过在计算中将细胞环境的特征(特别是许多衣壳围绕其组装的核酸的存在)添加到系统中,来预测这些与体外数据拟合的模拟中的组装会如何改变。此类工作的主要挑战在于计算方面:在真实病毒的规模和参数范围内模拟精细尺度的组装途径,计算成本过高,以至于无法建立核酸相互作用的显式模型。我们通过应用核酸效应的分析模型来绕过这一限制,调整从体外数据中获得的动力学速率参数,以观察这些调整单独或组合起来可能如何影响精细尺度的组装进程。由此产生的模拟结果展现出惊人的行为复杂性,不同的效应常常协同作用,以驱动高效组装并相对于体外模型改变组装途径。这项工作展示了计算机模拟如何帮助我们理解体外和体内环境中的组装可能有何不同,以及细胞环境的哪些特征导致了这些差异。