Ridgway Douglas, Broderick Gordon, Ellison Michael J
Institute for Biomolecular Design, University of Alberta, Edmonton, Alberta T6G 2H7, Canada.
Curr Opin Biotechnol. 2006 Oct;17(5):493-8. doi: 10.1016/j.copbio.2006.08.004. Epub 2006 Sep 8.
Interest in the possibility of dynamically simulating complex cellular processes has escalated markedly in recent years. This interest has been fuelled by three factors: the generally accepted value in understanding living processes as integrated systems; the dramatic increase in computational capability; and the availability of new or improved technology for making the quantitative measurements that are needed to drive and validate cellular simulations. Between the extremes of atom-scale and organism-scale simulation is a vast middle-ground requiring simulation strategies that are capable of dealing with a range of spatial, temporal and molecular abundance scales that are crucial for a comprehensive understanding of integrative cell biology. Although at an early stage, methodological improvements and the development of computational platforms provide some hope that simulations will emerge that can bridge the gap between network models and the true operation of the cell as a complex machine.
近年来,对动态模拟复杂细胞过程可能性的兴趣显著升温。这种兴趣受到三个因素的推动:将生命过程理解为整合系统的普遍公认价值;计算能力的大幅提升;以及用于进行驱动和验证细胞模拟所需的定量测量的新的或改进的技术的可用性。在原子尺度和生物体尺度模拟的两个极端之间,存在着广阔的中间地带,这需要能够处理一系列空间、时间和分子丰度尺度的模拟策略,而这些尺度对于全面理解整合细胞生物学至关重要。尽管尚处于早期阶段,但方法学的改进和计算平台的发展带来了一些希望,即将会出现能够弥合网络模型与作为复杂机器的细胞真实运作之间差距的模拟。