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模拟生物复杂性:一位物理科学家的视角

Modelling biological complexity: a physical scientist's perspective.

作者信息

Coveney Peter V, Fowler Philip W

机构信息

Centre for Computational Science, Department of Chemistry, University College London, Christopher Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, UK.

出版信息

J R Soc Interface. 2005 Sep 22;2(4):267-80. doi: 10.1098/rsif.2005.0045.

Abstract

We discuss the modern approaches of complexity and self-organization to understanding dynamical systems and how these concepts can inform current interest in systems biology. From the perspective of a physical scientist, it is especially interesting to examine how the differing weights given to philosophies of science in the physical and biological sciences impact the application of the study of complexity. We briefly describe how the dynamics of the heart and circadian rhythms, canonical examples of systems biology, are modelled by sets of nonlinear coupled differential equations, which have to be solved numerically. A major difficulty with this approach is that all the parameters within these equations are not usually known. Coupled models that include biomolecular detail could help solve this problem. Coupling models across large ranges of length- and time-scales is central to describing complex systems and therefore to biology. Such coupling may be performed in at least two different ways, which we refer to as hierarchical and hybrid multiscale modelling. While limited progress has been made in the former case, the latter is only beginning to be addressed systematically. These modelling methods are expected to bring numerous benefits to biology, for example, the properties of a system could be studied over a wider range of length- and time-scales, a key aim of systems biology. Multiscale models couple behaviour at the molecular biological level to that at the cellular level, thereby providing a route for calculating many unknown parameters as well as investigating the effects at, for example, the cellular level, of small changes at the biomolecular level, such as a genetic mutation or the presence of a drug. The modelling and simulation of biomolecular systems is itself very computationally intensive; we describe a recently developed hybrid continuum-molecular model, HybridMD, and its associated molecular insertion algorithm, which point the way towards the integration of molecular and more coarse-grained representations of matter. The scope of such integrative approaches to complex systems research is circumscribed by the computational resources available. Computational grids should provide a step jump in the scale of these resources; we describe the tools that RealityGrid, a major UK e-Science project, has developed together with our experience of deploying complex models on nascent grids. We also discuss the prospects for mathematical approaches to reducing the dimensionality of complex networks in the search for universal systems-level properties, illustrating our approach with a description of the origin of life according to the RNA world view.

摘要

我们讨论复杂性和自组织的现代方法如何用于理解动态系统,以及这些概念如何为当前对系统生物学的兴趣提供信息。从物理科学家的角度来看,研究物理科学和生物科学中给予科学哲学的不同权重如何影响复杂性研究的应用尤其有趣。我们简要描述了心脏动力学和昼夜节律(系统生物学的典型例子)是如何由一组非线性耦合微分方程建模的,这些方程必须通过数值求解。这种方法的一个主要困难是这些方程中的所有参数通常是未知的。包含生物分子细节的耦合模型可能有助于解决这个问题。跨越大范围长度和时间尺度的耦合模型对于描述复杂系统以及生物学来说至关重要。这种耦合至少可以通过两种不同的方式进行,我们将其称为分层多尺度建模和混合多尺度建模。虽然在前一种情况下取得的进展有限,但后一种情况才刚刚开始被系统地研究。这些建模方法有望给生物学带来诸多益处,例如,可以在更广泛的长度和时间尺度上研究系统的特性,这是系统生物学的一个关键目标。多尺度模型将分子生物学水平的行为与细胞水平的行为耦合起来,从而为计算许多未知参数以及研究生物分子水平的微小变化(如基因突变或药物存在)在细胞水平等方面的影响提供了一条途径。生物分子系统的建模和模拟本身计算量就很大;我们描述了一种最近开发的混合连续体 - 分子模型HybridMD及其相关的分子插入算法,它们为物质的分子表示和更粗粒度表示的整合指明了方向。这种复杂系统研究的综合方法的范围受到可用计算资源的限制。计算网格应该在这些资源的规模上实现一个飞跃;我们描述了英国一个主要的电子科学项目RealityGrid开发的工具以及我们在新生网格上部署复杂模型的经验。我们还讨论了在寻找通用系统级特性时,通过数学方法降低复杂网络维度的前景,并根据RNA世界观点描述生命起源来说明我们的方法。

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