Martini Mapper: An Automated Fragment-Based Mapping Algorithm for Developing Coarse-Grained Models within the Martini 3 Framework

Coarse-graining (CG) reduces molecular details to extend the time and length scales of molecular dynamics simulations to microseconds and micrometers. However, the CG approaches have long been limited by the difficulty of constructing both accurate and transferable models efficiently, considering the large diversity of chemical structures of materials. Among CG force fields, Martini is the most widely used, as it retains essential chemical features while offering substantial computational efficiency. Its most recent version, Martini 3, expands chemical resolution through a much broader bead set, particularly for small molecules. However, this flexibility also complicates the mapping of organic molecules because of context-dependent rules and the lack of standardized procedures. To address this issue, we present an automated framework that builds Martini 3 models directly from SMILES (Simplified Molecular Input Line Entry System) strings by combining a curated bead dictionary with a hierarchical, rule-based algorithm and molecule-specific bonded parameters. Our framework, Martini Mapper https://github.com/eliobaby/Martini_mapper, generated Martini 3 models for 6280 molecules across six chemically diverse data sets, including 1689 systems with bond/angle parameters and additional large systems mapped at the topological level. A curated subset of 1075 mapped structures was benchmarked using transfer free energies in hydrated octanol, hexadecane, and chloroform from water against reference data wherever available. We further examined the benchmark with structural validation via SASA, yielding good agreement with experimental and atomistic reference data. The workflow can also map large molecules containing up to 172 heavy atoms, exceeding the capabilities of existing automated approaches. Our framework, therefore, enables systematic and scalable Martini 3 structures for high-throughput simulations relevant to drug discovery and materials design.

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Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2026-04-28
DOI
https://doi.org/10.1021/acs.jcim.5c02903
Primary Topic
Machine Learning in Materials Science
Type
article
Field-Weighted Citation Impact
0.00

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article

Martini Mapper: An Automated Fragment-Based Mapping Algorithm for Developing Coarse-Grained Models within the Martini 3 Framework

Yaxin An, Kevin V. Bigting, Shubhadeep Nag
Journal of Chemical Information and Modeling
Machine Learning in Materials Science
article

Martini Mapper: An Automated Fragment-Based Mapping Algorithm for Developing Coarse-Grained Models within the Martini 3 Framework

Yaxin An, Kevin V. Bigting, Shubhadeep Nag
article en

Abstract

Coarse-graining (CG) reduces molecular details to extend the time and length scales of molecular dynamics simulations to microseconds and micrometers. However, the CG approaches have long been limited by the difficulty of constructing both accurate and transferable models efficiently, considering the large diversity of chemical structures of materials. Among CG force fields, Martini is the most widely used, as it retains essential chemical features while offering substantial computational efficiency. Its most recent version, Martini 3, expands chemical resolution through a much broader bead set, particularly for small molecules. However, this flexibility also complicates the mapping of organic molecules because of context-dependent rules and the lack of standardized procedures. To address this issue, we present an automated framework that builds Martini 3 models directly from SMILES (Simplified Molecular Input Line Entry System) strings by combining a curated bead dictionary with a hierarchical, rule-based algorithm and molecule-specific bonded parameters. Our framework, Martini Mapper https://github.com/eliobaby/Martini_mapper, generated Martini 3 models for 6280 molecules across six chemically diverse data sets, including 1689 systems with bond/angle parameters and additional large systems mapped at the topological level. A curated subset of 1075 mapped structures was benchmarked using transfer free energies in hydrated octanol, hexadecane, and chloroform from water against reference data wherever available. We further examined the benchmark with structural validation via SASA, yielding good agreement with experimental and atomistic reference data. The workflow can also map large molecules containing up to 172 heavy atoms, exceeding the capabilities of existing automated approaches. Our framework, therefore, enables systematic and scalable Martini 3 structures for high-throughput simulations relevant to drug discovery and materials design.

Journal of Chemical Information and ModelingVol. 66(9)
Louisiana State University (US)
National Science Foundation, Louisiana Board of Regents, Louisiana State University, Office of Integrative Activities
Openalex Percentile: Top 100%
Machine Learning in Materials Science
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