...
首页> 外文期刊>Journal of Computational and Nonlinear Dynamics >Modeling Flexibility in Myosin V Using a Multiscale Articulated Multi-Rigid Body Approach
【24h】

Modeling Flexibility in Myosin V Using a Multiscale Articulated Multi-Rigid Body Approach

机译:使用多尺度关节多刚体方法在Myosin V中建模灵活性

获取原文
获取原文并翻译 | 示例
           

摘要

This paper presents a multiscale dynamic model for the simulation and analysis of flexibility in myosin V. A 3D finite segment model, a multirigid body model connected with torsional springs, is developed to mechanically model the biological structure of myosin V. The long simulation run time is one of the most important issues in the dynamic modeling of biomolecules and proteins due to the disproportionality between the physical parameters involved in their dynamics. In order to address this issue, the most-used models, based on the famous overdamped Langevin equation, omit the inertial terms in the equations of motion; that leads to a first order model that is inconsistent with Newton's second law. However, the proposed model uses the concept of the method of multiple scales (MMS) that brings all of the terms of the equations of motion into proportion with each other; that helps to retain the inertia terms. This keeps the consistency of the model with the physical laws and experimental observations. In addition, the numerical integration's step size can be increased from commonly used subfemtoseconds to submilliseconds. Therefore, the simulation run time is significantly reduced in comparison with other approaches. The simulation results obtained by the proposed multiscale model show a dynamic behavior of myosin V which is more consistent with experimental observations in comparison with other overdamped models.
机译:本文提出了一种用于模拟和分析肌球蛋白V柔性的多尺度动力学模型。开发了3D有限段模型,即与扭转弹簧连接的多刚体模型,以机械方式建模了肌球蛋白V的生物学结构。由于涉及动态的物理参数之间的不成比例关系,是生物分子和蛋白质动态建模中最重要的问题之一。为了解决这个问题,基于著名的过阻尼兰格文方程的最常用模型在运动方程中省略了惯性项。这导致与牛顿第二定律不一致的一阶模型。但是,所提出的模型使用了多尺度方法(MMS)的概念,使运动方程的所有项相互成比例。这有助于保留惯性项。这样可以使模型与物理定律和实验观察保持一致。另外,数值积分的步长可以从常用的亚飞秒增加到亚毫秒。因此,与其他方法相比,仿真运行时间显着减少。通过提出的多尺度模型获得的仿真结果显示出肌球蛋白V的动态行为,与其他过阻尼模型相比,与实验观察结果更加一致。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号