Literature DB >> 34910495

Assembly and Analysis of Cell-Scale Membrane Envelopes.

Josh V Vermaas1,2, Christopher G Mayne2, Eric Shinn2, Emad Tajkhorshid2.   

Abstract

The march toward exascale computing will enable routine molecular simulation of larger and more complex systems, for example, simulation of entire viral particles, on the scale of approximately billions of atoms─a simulation size commensurate with a small bacterial cell. Anticipating the future hardware capabilities that will enable this type of research and paralleling advances in experimental structural biology, efforts are currently underway to develop software tools, procedures, and workflows for constructing cell-scale structures. Herein, we describe our efforts in developing and implementing an efficient and robust workflow for construction of cell-scale membrane envelopes and embedding membrane proteins into them. A new approach for construction of massive membrane structures that are stable during the simulations is built on implementing a subtractive assembly technique coupled with the development of a structure concatenation tool (fastmerge), which eliminates overlapping elements based on volumetric criteria rather than adding successive molecules to the simulation system. Using this approach, we have constructed two "protocells" consisting of MARTINI coarse-grained beads to represent cellular membranes, one the size of a cellular organelle and another the size of a small bacterial cell. The membrane envelopes constructed here remain whole during the molecular dynamics simulations performed and exhibit water flux only through specific proteins, demonstrating the success of our methodology in creating tight cell-like membrane compartments. Extended simulations of these cell-scale structures highlight the propensity for nonspecific interactions between adjacent membrane proteins leading to the formation of protein microclusters on the cell surface, an insight uniquely enabled by the scale of the simulations. We anticipate that the experiences and best practices presented here will form the basis for the next generation of cell-scale models, which will begin to address the addition of soluble proteins, nucleic acids, and small molecules essential to the function of a cell.

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Year:  2021        PMID: 34910495      PMCID: PMC8903035          DOI: 10.1021/acs.jcim.1c01050

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  105 in total

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Journal:  ACS Nano       Date:  2018-04-18       Impact factor: 15.881

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7.  CHARMM-GUI Martini Maker for Coarse-Grained Simulations with the Martini Force Field.

Authors:  Yifei Qi; Helgi I Ingólfsson; Xi Cheng; Jumin Lee; Siewert J Marrink; Wonpil Im
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  2 in total

Review 1.  Organelle Interaction and Drug Discovery: Towards Correlative Nanoscopy and Molecular Dynamics Simulation.

Authors:  Zhiwei Yang; Zichen Zhang; Yizhen Zhao; Qiushi Ye; Xuhua Li; Lingjie Meng; Jiangang Long; Shengli Zhang; Lei Zhang
Journal:  Front Pharmacol       Date:  2022-06-20       Impact factor: 5.988

2.  Breathing and tilting: mesoscale simulations illuminate influenza glycoprotein vulnerabilities.

Authors:  Lorenzo Casalino; Christian Seitz; Julia Lederhofer; Yaroslav Tsybovsky; Ian A Wilson; Masaru Kanekiyo; Rommie E Amaro
Journal:  bioRxiv       Date:  2022-08-07
  2 in total

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