4.6 Article

SMOG 2 and OpenSMOG: Extending the limits of structure-based models

期刊

PROTEIN SCIENCE
卷 31, 期 1, 页码 158-172

出版社

WILEY
DOI: 10.1002/pro.4209

关键词

assemblies; DNA; energy landscape; protein; RNA; simulation

资金

  1. National Science Foundation, Division of Molecular and Cellular Biosciences [1915843]
  2. National Science Foundation, Division of Chemistry [1614101]
  3. National Science Foundation, Division of Physics [1522550, 2019745]
  4. Welch Foundation [C-1792]
  5. Div Of Molecular and Cellular Bioscience
  6. Direct For Biological Sciences [1614101, 1915843] Funding Source: National Science Foundation

向作者/读者索取更多资源

Simulations with structure-based models have been effective in investigating factors that control biomolecular dynamics, and SMOG 2 provides robust support for developing and applying such models.
Applying simulations with structure-based (Go over bar -like) models has proven to be an effective strategy for investigating the factors that control biomolecular dynamics. The common element of these models is that some (or all) of the intra/inter-molecular interactions are explicitly defined to stabilize an experimentally determined structure. To facilitate the development and application of this broad class of models, we previously released the SMOG 2 software package. This suite allows one to easily customize and distribute structure-based (i.e., SMOG) models for any type of polymer-ligand system. The force fields generated by SMOG 2 may then be used to perform simulations in highly optimized MD packages, such as Gromacs, NAMD, LAMMPS, and OpenMM. Here, we describe extensions to the software and demonstrate the capabilities of the most recent version (SMOG v2.4.2). Changes include new tools that aid user-defined customization of force fields, as well as an interface with the OpenMM simulation libraries (OpenSMOG v1.1.0). The OpenSMOG module allows for arbitrary user-defined contact potentials and non-bonded potentials to be employed in SMOG models, without source-code modifications. To illustrate the utility of these advances, we present applications to systems with millions of atoms, long polymers and explicit ions, as well as models that include non-structure-based (e.g., AMBER-based) energetic terms. Examples include large-scale rearrangements of the SARS-CoV-2 Spike protein, the HIV-1 capsid with explicit ions, and crystallographic lattices of ribosomes and proteins. In summary, SMOG 2 and OpenSMOG provide robust support for researchers who seek to develop and apply structure-based models to large and/or intricate biomolecular systems.

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