Asynchronous Reciprocal Coupling of Martini 2.2 Coarse-Grained and CHARMM36 All-Atom Simulations in an Automated Multiscale Framework

The appeal of multiscale modeling approaches is predicated on the promise of combinatorial synergy. However, this promise can only be realized when distinct scales are combined with reciprocal consistency. Here, we consider multiscale molecular dynamics (MD) simulations that combine the accuracy and...

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Veröffentlicht in:Journal of chemical theory and computation 2022-08, Vol.18 (8), p.5025-5045
Hauptverfasser: López, Cesar A., Zhang, Xiaohua, Aydin, Fikret, Shrestha, Rebika, Van, Que N., Stanley, Christopher B., Carpenter, Timothy S., Nguyen, Kien, Patel, Lara A., Chen, De, Burns, Violetta, Hengartner, Nicolas W., Reddy, Tyler J. E., Bhatia, Harsh, Di Natale, Francesco, Tran, Timothy H., Chan, Albert H., Simanshu, Dhirendra K., Nissley, Dwight V., Streitz, Frederick H., Stephen, Andrew G., Turbyville, Thomas J., Lightstone, Felice C., Gnanakaran, Sandrasegaram, Ingólfsson, Helgi I., Neale, Chris
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container_end_page 5045
container_issue 8
container_start_page 5025
container_title Journal of chemical theory and computation
container_volume 18
creator López, Cesar A.
Zhang, Xiaohua
Aydin, Fikret
Shrestha, Rebika
Van, Que N.
Stanley, Christopher B.
Carpenter, Timothy S.
Nguyen, Kien
Patel, Lara A.
Chen, De
Burns, Violetta
Hengartner, Nicolas W.
Reddy, Tyler J. E.
Bhatia, Harsh
Di Natale, Francesco
Tran, Timothy H.
Chan, Albert H.
Simanshu, Dhirendra K.
Nissley, Dwight V.
Streitz, Frederick H.
Stephen, Andrew G.
Turbyville, Thomas J.
Lightstone, Felice C.
Gnanakaran, Sandrasegaram
Ingólfsson, Helgi I.
Neale, Chris
description The appeal of multiscale modeling approaches is predicated on the promise of combinatorial synergy. However, this promise can only be realized when distinct scales are combined with reciprocal consistency. Here, we consider multiscale molecular dynamics (MD) simulations that combine the accuracy and macromolecular flexibility accessible to fixed-charge all-atom (AA) representations with the sampling speed accessible to reductive, coarse-grained (CG) representations. AA-to-CG conversions are relatively straightforward because deterministic routines with unique outcomes are achievable. Conversely, CG-to-AA conversions have many solutions due to a surge in the number of degrees of freedom. While automated tools for biomolecular CG-to-AA transformation exist, we find that one popular option, called Backward, is prone to stochastic failure and the AA models that it does generate frequently have compromised protein structure and incorrect stereochemistry. Although these shortcomings can likely be circumvented by human intervention in isolated instances, automated multiscale coupling requires reliable and robust scale conversion. Here, we detail an extension to Multiscale Machine-learned Modeling Infrastructure (MuMMI), including an improved CG-to-AA conversion tool called sinceCG. This tool is reliable (∼98% weakly correlated repeat success rate), automatable (no unrecoverable hangs), and yields AA models that generally preserve protein secondary structure and maintain correct stereochemistry. We describe how the MuMMI framework identifies CG system configurations of interest, converts them to AA representations, and simulates them at the AA scale while on-the-fly analyses provide feedback to update CG parameters. Application to systems containing the peripheral membrane protein RAS and proximal components of RAF kinase on complex eight-component lipid bilayers with ∼1.5 million atoms is discussed in the context of MuMMI.
doi_str_mv 10.1021/acs.jctc.2c00168
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E. ; Bhatia, Harsh ; Di Natale, Francesco ; Tran, Timothy H. ; Chan, Albert H. ; Simanshu, Dhirendra K. ; Nissley, Dwight V. ; Streitz, Frederick H. ; Stephen, Andrew G. ; Turbyville, Thomas J. ; Lightstone, Felice C. ; Gnanakaran, Sandrasegaram ; Ingólfsson, Helgi I. ; Neale, Chris</creator><creatorcontrib>López, Cesar A. ; Zhang, Xiaohua ; Aydin, Fikret ; Shrestha, Rebika ; Van, Que N. ; Stanley, Christopher B. ; Carpenter, Timothy S. ; Nguyen, Kien ; Patel, Lara A. ; Chen, De ; Burns, Violetta ; Hengartner, Nicolas W. ; Reddy, Tyler J. E. ; Bhatia, Harsh ; Di Natale, Francesco ; Tran, Timothy H. ; Chan, Albert H. ; Simanshu, Dhirendra K. ; Nissley, Dwight V. ; Streitz, Frederick H. ; Stephen, Andrew G. ; Turbyville, Thomas J. ; Lightstone, Felice C. ; Gnanakaran, Sandrasegaram ; Ingólfsson, Helgi I. ; Neale, Chris ; Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States) ; Los Alamos National Laboratory (LANL), Los Alamos, NM (United States) ; Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States) ; Frederick National Lab. for Cancer Research, Frederick, MD (United States)</creatorcontrib><description>The appeal of multiscale modeling approaches is predicated on the promise of combinatorial synergy. However, this promise can only be realized when distinct scales are combined with reciprocal consistency. 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Here, we detail an extension to Multiscale Machine-learned Modeling Infrastructure (MuMMI), including an improved CG-to-AA conversion tool called sinceCG. This tool is reliable (∼98% weakly correlated repeat success rate), automatable (no unrecoverable hangs), and yields AA models that generally preserve protein secondary structure and maintain correct stereochemistry. We describe how the MuMMI framework identifies CG system configurations of interest, converts them to AA representations, and simulates them at the AA scale while on-the-fly analyses provide feedback to update CG parameters. 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We describe how the MuMMI framework identifies CG system configurations of interest, converts them to AA representations, and simulates them at the AA scale while on-the-fly analyses provide feedback to update CG parameters. 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E. ; Bhatia, Harsh ; Di Natale, Francesco ; Tran, Timothy H. ; Chan, Albert H. ; Simanshu, Dhirendra K. ; Nissley, Dwight V. ; Streitz, Frederick H. ; Stephen, Andrew G. ; Turbyville, Thomas J. ; Lightstone, Felice C. ; Gnanakaran, Sandrasegaram ; Ingólfsson, Helgi I. ; Neale, Chris</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a410t-16a4ebe2b0738901699d5d12028d177457ace55811d367e6b32c3207accab2143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Accessibility</topic><topic>Automation</topic><topic>Biomolecular Systems</topic><topic>Combinatorial analysis</topic><topic>Conversion</topic><topic>INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</topic><topic>Kinases</topic><topic>Lipids</topic><topic>Modelling</topic><topic>Molecular dynamics</topic><topic>Proteins</topic><topic>Representations</topic><topic>Simulation</topic><topic>Stereochemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>López, Cesar A.</creatorcontrib><creatorcontrib>Zhang, Xiaohua</creatorcontrib><creatorcontrib>Aydin, Fikret</creatorcontrib><creatorcontrib>Shrestha, Rebika</creatorcontrib><creatorcontrib>Van, Que N.</creatorcontrib><creatorcontrib>Stanley, Christopher B.</creatorcontrib><creatorcontrib>Carpenter, Timothy S.</creatorcontrib><creatorcontrib>Nguyen, Kien</creatorcontrib><creatorcontrib>Patel, Lara A.</creatorcontrib><creatorcontrib>Chen, De</creatorcontrib><creatorcontrib>Burns, Violetta</creatorcontrib><creatorcontrib>Hengartner, Nicolas W.</creatorcontrib><creatorcontrib>Reddy, Tyler J. 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E.</au><au>Bhatia, Harsh</au><au>Di Natale, Francesco</au><au>Tran, Timothy H.</au><au>Chan, Albert H.</au><au>Simanshu, Dhirendra K.</au><au>Nissley, Dwight V.</au><au>Streitz, Frederick H.</au><au>Stephen, Andrew G.</au><au>Turbyville, Thomas J.</au><au>Lightstone, Felice C.</au><au>Gnanakaran, Sandrasegaram</au><au>Ingólfsson, Helgi I.</au><au>Neale, Chris</au><aucorp>Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)</aucorp><aucorp>Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)</aucorp><aucorp>Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)</aucorp><aucorp>Frederick National Lab. for Cancer Research, Frederick, MD (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asynchronous Reciprocal Coupling of Martini 2.2 Coarse-Grained and CHARMM36 All-Atom Simulations in an Automated Multiscale Framework</atitle><jtitle>Journal of chemical theory and computation</jtitle><addtitle>J. Chem. Theory Comput</addtitle><date>2022-08-09</date><risdate>2022</risdate><volume>18</volume><issue>8</issue><spage>5025</spage><epage>5045</epage><pages>5025-5045</pages><issn>1549-9618</issn><eissn>1549-9626</eissn><abstract>The appeal of multiscale modeling approaches is predicated on the promise of combinatorial synergy. However, this promise can only be realized when distinct scales are combined with reciprocal consistency. Here, we consider multiscale molecular dynamics (MD) simulations that combine the accuracy and macromolecular flexibility accessible to fixed-charge all-atom (AA) representations with the sampling speed accessible to reductive, coarse-grained (CG) representations. AA-to-CG conversions are relatively straightforward because deterministic routines with unique outcomes are achievable. Conversely, CG-to-AA conversions have many solutions due to a surge in the number of degrees of freedom. While automated tools for biomolecular CG-to-AA transformation exist, we find that one popular option, called Backward, is prone to stochastic failure and the AA models that it does generate frequently have compromised protein structure and incorrect stereochemistry. Although these shortcomings can likely be circumvented by human intervention in isolated instances, automated multiscale coupling requires reliable and robust scale conversion. Here, we detail an extension to Multiscale Machine-learned Modeling Infrastructure (MuMMI), including an improved CG-to-AA conversion tool called sinceCG. This tool is reliable (∼98% weakly correlated repeat success rate), automatable (no unrecoverable hangs), and yields AA models that generally preserve protein secondary structure and maintain correct stereochemistry. We describe how the MuMMI framework identifies CG system configurations of interest, converts them to AA representations, and simulates them at the AA scale while on-the-fly analyses provide feedback to update CG parameters. Application to systems containing the peripheral membrane protein RAS and proximal components of RAF kinase on complex eight-component lipid bilayers with ∼1.5 million atoms is discussed in the context of MuMMI.</abstract><cop>Washington</cop><pub>American Chemical Society</pub><doi>10.1021/acs.jctc.2c00168</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0003-3237-8043</orcidid><orcidid>https://orcid.org/0000-0001-7523-116X</orcidid><orcidid>https://orcid.org/0000-0001-7848-9983</orcidid><orcidid>https://orcid.org/0000-0001-8712-7773</orcidid><orcidid>https://orcid.org/0000-0001-9912-078X</orcidid><orcidid>https://orcid.org/0000-0002-9368-3044</orcidid><orcidid>https://orcid.org/0000-0002-4226-7710</orcidid><orcidid>https://orcid.org/000000024157134X</orcidid><orcidid>https://orcid.org/0000000293683044</orcidid><orcidid>https://orcid.org/0000000317042445</orcidid><orcidid>https://orcid.org/0000000323646157</orcidid><orcidid>https://orcid.org/0000000178489983</orcidid><orcidid>https://orcid.org/0000000332378043</orcidid><orcidid>https://orcid.org/000000019912078X</orcidid><orcidid>https://orcid.org/0000000187127773</orcidid><orcidid>https://orcid.org/000000017523116X</orcidid><orcidid>https://orcid.org/0000000346843364</orcidid><orcidid>https://orcid.org/0000000242267710</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1549-9618
ispartof Journal of chemical theory and computation, 2022-08, Vol.18 (8), p.5025-5045
issn 1549-9618
1549-9626
language eng
recordid cdi_osti_scitechconnect_1885350
source American Chemical Society Journals
subjects Accessibility
Automation
Biomolecular Systems
Combinatorial analysis
Conversion
INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Kinases
Lipids
Modelling
Molecular dynamics
Proteins
Representations
Simulation
Stereochemistry
title Asynchronous Reciprocal Coupling of Martini 2.2 Coarse-Grained and CHARMM36 All-Atom Simulations in an Automated Multiscale Framework
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