MOLECULAR DYNAMICS SIMULATIONS AND METHOD DEVELOPMENT

这个子项目是利用由NIH/NCRR资助的中心拨款提供的资源的许多研究子项目之一。子项目和调查员(PI)可能从另一个NIH来源获得了主要资金，因此可能会出现在其他CRISE条目中。列出的机构是针对中心的，而不一定是针对调查员的机构。我们使用计算机图形学实验室的设施来显示和分析分子动力学模拟结果。我们的研究项目集中在a)提炼、测试和开发新一代添加和非添加的力场参数；以及b)使用分子动力学进行大分子模拟。这项工作正在进行中，以进一步开发添加和非添加琥珀力场。非加性琥珀参数化包括基于原子极化率的非加性效应和孤子对相互作用。提出了一种处理非加性模拟电荷发展过程中分子内极化的新方法。在DNA和小蛋白质上进行了更彻底的测试，使用位于给电子原子上的额外偏心(孤对)点的非加性力场。此外，还对泛素和短聚丙氨酸肽等小蛋白进行了更多的测试。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. We use the Computer Graphics Laboratory facilities to display and analyze molecular dynamics simulation results. Our research projects focus on a) refining, testing and developing the new generation of additive and nonadditive force field parameters; and b) macromolecular simulation using molecular dynamics. The work is being carried out to further develop the additive and nonadditive AMBER force field. The nonadditive AMBER parametrization includes nonadditive effects, based on atomic polarizabilities, and lone pairs interactions. A new approach to treat intra-molecular polarization has been proposed during charge development for nonadditive simulations. More thorough tests have been performed on DNA and small proteins using nonadditive force field with additional off-center (lone pairs) points located on electron-donating atoms. Additionally more tests have been performed on small protein such as ubiquitin, and short polyalanine peptides.