Cargando…
Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition
Molybdenum disulfide (MoS(2)) is a layered material with outstanding electrical and optical properties. Numerous studies evaluate the performance in sensors, catalysts, batteries, and composites that can benefit from guidance by simulations in all-atom resolution. However, molecular simulations rema...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162032/ https://www.ncbi.nlm.nih.gov/pubmed/34094188 http://dx.doi.org/10.1039/d0sc01443e |
_version_ | 1783700631894097920 |
---|---|
author | Liu, Juan Zeng, Jin Zhu, Cheng Miao, Jianwei Huang, Yu Heinz, Hendrik |
author_facet | Liu, Juan Zeng, Jin Zhu, Cheng Miao, Jianwei Huang, Yu Heinz, Hendrik |
author_sort | Liu, Juan |
collection | PubMed |
description | Molybdenum disulfide (MoS(2)) is a layered material with outstanding electrical and optical properties. Numerous studies evaluate the performance in sensors, catalysts, batteries, and composites that can benefit from guidance by simulations in all-atom resolution. However, molecular simulations remain difficult due to lack of reliable models. We introduce an interpretable force field for MoS(2) with record performance that reproduces structural, interfacial, and mechanical properties in 0.1% to 5% agreement with experiments. The model overcomes structural instability, deviations in interfacial and mechanical properties by several 100%, and empirical fitting protocols in earlier models. It is compatible with several force fields for molecular dynamics simulation, including the interface force field (IFF), CVFF, DREIDING, PCFF, COMPASS, CHARMM, AMBER, and OPLS-AA. The parameters capture polar covalent bonding, X-ray structure, cleavage energy, infrared spectra, bending stability, bulk modulus, Young's modulus, and contact angles with polar and nonpolar solvents. We utilized the models to uncover the binding mechanism of peptides to the MoS(2) basal plane. The binding strength of several 7mer and 8mer peptides scales linearly with surface contact and replacement of surface-bound water molecules, and is tunable in a wide range from −86 to −6 kcal mol(−1). The binding selectivity is multifactorial, including major contributions by van-der-Waals coordination and charge matching of certain side groups, orientation of hydrophilic side chains towards water, and conformation flexibility. We explain the relative attraction and role of the 20 amino acids using computational and experimental data. The force field can be used to screen and interpret the assembly of MoS(2)-based nanomaterials and electrolyte interfaces up to a billion atoms with high accuracy, including multiscale simulations from the quantum scale to the microscale. |
format | Online Article Text |
id | pubmed-8162032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81620322021-06-04 Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition Liu, Juan Zeng, Jin Zhu, Cheng Miao, Jianwei Huang, Yu Heinz, Hendrik Chem Sci Chemistry Molybdenum disulfide (MoS(2)) is a layered material with outstanding electrical and optical properties. Numerous studies evaluate the performance in sensors, catalysts, batteries, and composites that can benefit from guidance by simulations in all-atom resolution. However, molecular simulations remain difficult due to lack of reliable models. We introduce an interpretable force field for MoS(2) with record performance that reproduces structural, interfacial, and mechanical properties in 0.1% to 5% agreement with experiments. The model overcomes structural instability, deviations in interfacial and mechanical properties by several 100%, and empirical fitting protocols in earlier models. It is compatible with several force fields for molecular dynamics simulation, including the interface force field (IFF), CVFF, DREIDING, PCFF, COMPASS, CHARMM, AMBER, and OPLS-AA. The parameters capture polar covalent bonding, X-ray structure, cleavage energy, infrared spectra, bending stability, bulk modulus, Young's modulus, and contact angles with polar and nonpolar solvents. We utilized the models to uncover the binding mechanism of peptides to the MoS(2) basal plane. The binding strength of several 7mer and 8mer peptides scales linearly with surface contact and replacement of surface-bound water molecules, and is tunable in a wide range from −86 to −6 kcal mol(−1). The binding selectivity is multifactorial, including major contributions by van-der-Waals coordination and charge matching of certain side groups, orientation of hydrophilic side chains towards water, and conformation flexibility. We explain the relative attraction and role of the 20 amino acids using computational and experimental data. The force field can be used to screen and interpret the assembly of MoS(2)-based nanomaterials and electrolyte interfaces up to a billion atoms with high accuracy, including multiscale simulations from the quantum scale to the microscale. The Royal Society of Chemistry 2020-07-21 /pmc/articles/PMC8162032/ /pubmed/34094188 http://dx.doi.org/10.1039/d0sc01443e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Liu, Juan Zeng, Jin Zhu, Cheng Miao, Jianwei Huang, Yu Heinz, Hendrik Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
title | Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
title_full | Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
title_fullStr | Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
title_full_unstemmed | Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
title_short | Interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
title_sort | interpretable molecular models for molybdenum disulfide and insight into selective peptide recognition |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162032/ https://www.ncbi.nlm.nih.gov/pubmed/34094188 http://dx.doi.org/10.1039/d0sc01443e |
work_keys_str_mv | AT liujuan interpretablemolecularmodelsformolybdenumdisulfideandinsightintoselectivepeptiderecognition AT zengjin interpretablemolecularmodelsformolybdenumdisulfideandinsightintoselectivepeptiderecognition AT zhucheng interpretablemolecularmodelsformolybdenumdisulfideandinsightintoselectivepeptiderecognition AT miaojianwei interpretablemolecularmodelsformolybdenumdisulfideandinsightintoselectivepeptiderecognition AT huangyu interpretablemolecularmodelsformolybdenumdisulfideandinsightintoselectivepeptiderecognition AT heinzhendrik interpretablemolecularmodelsformolybdenumdisulfideandinsightintoselectivepeptiderecognition |