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Ribosome flow model with nonhomogeneous site sizes

机译:具有非均匀部位尺寸的核糖体流动模型

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We introduce and analyze two general dynamical models for unidirectional movement of particles along a circular and an open chain of sites. The models include a soft version of the simple exclusion principle, thus allowing to model and analyze the evolution of "traffic jams" of particles along the chain. A unique feature of these two new models is that each site along the chain may have a different size. Although nonlinear, the models are amenable to rigorous analysis. We prove that the dynamics always converges to a steady-state, and that the steady-state densities along the chain and the steady-state output flow rate can be derived from the spectral properties of a suitable matrix, thus eliminating the need to numerically simulate the dynamics until convergence. This spectral representation also allows for powerful sensitivity analysis, i.e. understanding how a change in one of the parameters affects the steady-state. The site sizes and the transition rates from site to site play different roles in the dynamics, and for the purpose of maximizing the steady-state output (or production) rate the site sizes are more important than the transition rates. The new models can be applied to study various natural and artificial systems including networks of ribosome flow during mRNA translation, phosphorelay, the movement of molecular motors along filaments of the cytoskeleton, and pedestrian and vehicular traffic.
机译:我们介绍并分析了沿圆形和开放的位点颗粒的单向运动的两个通用动态模型。该模型包括简单排除原理的软版本,从而允许模拟并分析链条颗粒的“交通拥堵”的演变。这两个新型号的独特特征是沿着链条的每个站点可能具有不同的尺寸。虽然非线性,模型可用于严格分析。我们证明动态总是会聚到稳态,并且可以从合适矩阵的光谱特性导出沿链条和稳态输出流量的稳态密度,从而消除了数字模拟的需要动态直到收敛。该光谱表示还允许强大的灵敏度分析,即了解其中一个参数的变化如何影响稳态。从站点到现场的站点大小和转换率在动态中发挥不同的角色,出于最大化稳态输出(或生产)的目的,网站大小比过渡率更重要。新模型可用于研究各种自然和人工系统,包括mRNA翻译,phosphorelay,分子马达沿着细胞骨架的细丝的运动,行人和车辆在核糖体流的网络。

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