Automatic Optimization of Lipid Models in the Martini Force Field Using SwarmCG
After two decades of continued development of the Martini coarse-grained force field (CG FF), further refinment of the already rather accurate Martini lipid models has become a demanding task that could benefit from integrative data-driven methods. Automatic approaches are increasingly used in the d...
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Veröffentlicht in: | Journal of chemical information and modeling 2023-06, Vol.63 (12), p.3827-3838 |
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creator | Empereur-mot, Charly Pedersen, Kasper B. Capelli, Riccardo Crippa, Martina Caruso, Cristina Perrone, Mattia Souza, Paulo C. T. Marrink, Siewert J. Pavan, Giovanni M. |
description | After two decades of continued development of the Martini coarse-grained force field (CG FF), further refinment of the already rather accurate Martini lipid models has become a demanding task that could benefit from integrative data-driven methods. Automatic approaches are increasingly used in the development of accurate molecular models, but they typically make use of specifically designed interaction potentials that transfer poorly to molecular systems or conditions different than those used for model calibration. As a proof of concept, here, we employ SwarmCG, an automatic multiobjective optimization approach facilitating the development of lipid force fields, to refine specifically the bonded interaction parameters in building blocks of lipid models within the framework of the general Martini CG FF. As targets of the optimization procedure, we employ both experimental observables (top-down references: area per lipid and bilayer thickness) and all-atom molecular dynamics simulations (bottom-up reference), which respectively inform on the supra-molecular structure of the lipid bilayer systems and on their submolecular dynamics. In our training sets, we simulate at different temperatures in the liquid and gel phases up to 11 homogeneous lamellar bilayers composed of phosphatidylcholine lipids spanning various tail lengths and degrees of (un)saturation. We explore different CG representations of the molecules and evaluate improvements a posteriori using additional simulation temperatures and a portion of the phase diagram of a DOPC/DPPC mixture. Successfully optimizing up to ∼80 model parameters within still limited computational budgets, we show that this protocol allows the obtainment of improved transferable Martini lipid models. In particular, the results of this study demonstrate how a fine-tuning of the representation and parameters of the models may improve their accuracy and how automatic approaches, such as SwarmCG, may be very useful to this end. |
doi_str_mv | 10.1021/acs.jcim.3c00530 |
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T. ; Marrink, Siewert J. ; Pavan, Giovanni M.</creator><creatorcontrib>Empereur-mot, Charly ; Pedersen, Kasper B. ; Capelli, Riccardo ; Crippa, Martina ; Caruso, Cristina ; Perrone, Mattia ; Souza, Paulo C. T. ; Marrink, Siewert J. ; Pavan, Giovanni M.</creatorcontrib><description>After two decades of continued development of the Martini coarse-grained force field (CG FF), further refinment of the already rather accurate Martini lipid models has become a demanding task that could benefit from integrative data-driven methods. Automatic approaches are increasingly used in the development of accurate molecular models, but they typically make use of specifically designed interaction potentials that transfer poorly to molecular systems or conditions different than those used for model calibration. As a proof of concept, here, we employ SwarmCG, an automatic multiobjective optimization approach facilitating the development of lipid force fields, to refine specifically the bonded interaction parameters in building blocks of lipid models within the framework of the general Martini CG FF. As targets of the optimization procedure, we employ both experimental observables (top-down references: area per lipid and bilayer thickness) and all-atom molecular dynamics simulations (bottom-up reference), which respectively inform on the supra-molecular structure of the lipid bilayer systems and on their submolecular dynamics. In our training sets, we simulate at different temperatures in the liquid and gel phases up to 11 homogeneous lamellar bilayers composed of phosphatidylcholine lipids spanning various tail lengths and degrees of (un)saturation. We explore different CG representations of the molecules and evaluate improvements a posteriori using additional simulation temperatures and a portion of the phase diagram of a DOPC/DPPC mixture. Successfully optimizing up to ∼80 model parameters within still limited computational budgets, we show that this protocol allows the obtainment of improved transferable Martini lipid models. In particular, the results of this study demonstrate how a fine-tuning of the representation and parameters of the models may improve their accuracy and how automatic approaches, such as SwarmCG, may be very useful to this end.</description><identifier>ISSN: 1549-9596</identifier><identifier>EISSN: 1549-960X</identifier><identifier>DOI: 10.1021/acs.jcim.3c00530</identifier><identifier>PMID: 37279107</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Chemical Sciences ; Computational Chemistry ; Computer Science ; Interaction parameters ; Lipid Bilayers - chemistry ; Lipids ; Mathematical models ; Modeling and Simulation ; Molecular dynamics ; Molecular Dynamics Simulation ; Molecular structure ; Multiple objective analysis ; Optimization ; or physical chemistry ; Phase diagrams ; Phosphatidylcholine ; Phosphatidylcholines - chemistry ; Representations ; Simulation ; Temperature ; Theoretical and</subject><ispartof>Journal of chemical information and modeling, 2023-06, Vol.63 (12), p.3827-3838</ispartof><rights>2023 The Authors. Published by American Chemical Society</rights><rights>Copyright American Chemical Society Jun 26, 2023</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2023 The Authors. 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T.</creatorcontrib><creatorcontrib>Marrink, Siewert J.</creatorcontrib><creatorcontrib>Pavan, Giovanni M.</creatorcontrib><title>Automatic Optimization of Lipid Models in the Martini Force Field Using SwarmCG</title><title>Journal of chemical information and modeling</title><addtitle>J. Chem. Inf. Model</addtitle><description>After two decades of continued development of the Martini coarse-grained force field (CG FF), further refinment of the already rather accurate Martini lipid models has become a demanding task that could benefit from integrative data-driven methods. Automatic approaches are increasingly used in the development of accurate molecular models, but they typically make use of specifically designed interaction potentials that transfer poorly to molecular systems or conditions different than those used for model calibration. As a proof of concept, here, we employ SwarmCG, an automatic multiobjective optimization approach facilitating the development of lipid force fields, to refine specifically the bonded interaction parameters in building blocks of lipid models within the framework of the general Martini CG FF. As targets of the optimization procedure, we employ both experimental observables (top-down references: area per lipid and bilayer thickness) and all-atom molecular dynamics simulations (bottom-up reference), which respectively inform on the supra-molecular structure of the lipid bilayer systems and on their submolecular dynamics. In our training sets, we simulate at different temperatures in the liquid and gel phases up to 11 homogeneous lamellar bilayers composed of phosphatidylcholine lipids spanning various tail lengths and degrees of (un)saturation. We explore different CG representations of the molecules and evaluate improvements a posteriori using additional simulation temperatures and a portion of the phase diagram of a DOPC/DPPC mixture. Successfully optimizing up to ∼80 model parameters within still limited computational budgets, we show that this protocol allows the obtainment of improved transferable Martini lipid models. 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T.</au><au>Marrink, Siewert J.</au><au>Pavan, Giovanni M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automatic Optimization of Lipid Models in the Martini Force Field Using SwarmCG</atitle><jtitle>Journal of chemical information and modeling</jtitle><addtitle>J. Chem. Inf. Model</addtitle><date>2023-06-26</date><risdate>2023</risdate><volume>63</volume><issue>12</issue><spage>3827</spage><epage>3838</epage><pages>3827-3838</pages><issn>1549-9596</issn><eissn>1549-960X</eissn><abstract>After two decades of continued development of the Martini coarse-grained force field (CG FF), further refinment of the already rather accurate Martini lipid models has become a demanding task that could benefit from integrative data-driven methods. Automatic approaches are increasingly used in the development of accurate molecular models, but they typically make use of specifically designed interaction potentials that transfer poorly to molecular systems or conditions different than those used for model calibration. As a proof of concept, here, we employ SwarmCG, an automatic multiobjective optimization approach facilitating the development of lipid force fields, to refine specifically the bonded interaction parameters in building blocks of lipid models within the framework of the general Martini CG FF. As targets of the optimization procedure, we employ both experimental observables (top-down references: area per lipid and bilayer thickness) and all-atom molecular dynamics simulations (bottom-up reference), which respectively inform on the supra-molecular structure of the lipid bilayer systems and on their submolecular dynamics. In our training sets, we simulate at different temperatures in the liquid and gel phases up to 11 homogeneous lamellar bilayers composed of phosphatidylcholine lipids spanning various tail lengths and degrees of (un)saturation. We explore different CG representations of the molecules and evaluate improvements a posteriori using additional simulation temperatures and a portion of the phase diagram of a DOPC/DPPC mixture. Successfully optimizing up to ∼80 model parameters within still limited computational budgets, we show that this protocol allows the obtainment of improved transferable Martini lipid models. 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subjects | Chemical Sciences Computational Chemistry Computer Science Interaction parameters Lipid Bilayers - chemistry Lipids Mathematical models Modeling and Simulation Molecular dynamics Molecular Dynamics Simulation Molecular structure Multiple objective analysis Optimization or physical chemistry Phase diagrams Phosphatidylcholine Phosphatidylcholines - chemistry Representations Simulation Temperature Theoretical and |
title | Automatic Optimization of Lipid Models in the Martini Force Field Using SwarmCG |
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