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Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies
We perform molecular dynamics simulation on several relevant biological fibrils associated with neurodegenerative diseases such as Aβ(40), Aβ(42), and α-synuclein systems to obtain a molecular understanding and interpretation of nanomechanical characterization experiments. The computational method i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404408/ https://www.ncbi.nlm.nih.gov/pubmed/30873322 http://dx.doi.org/10.3762/bjnano.10.51 |
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author | Poma, Adolfo B Guzman, Horacio V Li, Mai Suan Theodorakis, Panagiotis E |
author_facet | Poma, Adolfo B Guzman, Horacio V Li, Mai Suan Theodorakis, Panagiotis E |
author_sort | Poma, Adolfo B |
collection | PubMed |
description | We perform molecular dynamics simulation on several relevant biological fibrils associated with neurodegenerative diseases such as Aβ(40), Aβ(42), and α-synuclein systems to obtain a molecular understanding and interpretation of nanomechanical characterization experiments. The computational method is versatile and addresses a new subarea within the mechanical characterization of heterogeneous soft materials. We investigate both the elastic and thermodynamic properties of the biological fibrils in order to substantiate experimental nanomechanical characterization techniques that are quickly developing and reaching dynamic imaging with video rate capabilities. The computational method qualitatively reproduces results of experiments with biological fibrils, validating its use in extrapolation to macroscopic material properties. Our computational techniques can be used for the co-design of new experiments aiming to unveil nanomechanical properties of biological fibrils from a point of view of molecular understanding. Our approach allows a comparison of diverse elastic properties based on different deformations , i.e., tensile (Y(L)), shear (S), and indentation (Y(T)) deformation. From our analysis, we find a significant elastic anisotropy between axial and transverse directions (i.e., Y(T) > Y(L)) for all systems. Interestingly, our results indicate a higher mechanostability of Aβ(42) fibrils compared to Aβ(40), suggesting a significant correlation between mechanical stability and aggregation propensity (rate) in amyloid systems. That is, the higher the mechanical stability the faster the fibril formation. Finally, we find that α-synuclein fibrils are thermally less stable than β-amyloid fibrils. We anticipate that our molecular-level analysis of the mechanical response under different deformation conditions for the range of fibrils considered here will provide significant insights for the experimental observations. |
format | Online Article Text |
id | pubmed-6404408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-64044082019-03-14 Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies Poma, Adolfo B Guzman, Horacio V Li, Mai Suan Theodorakis, Panagiotis E Beilstein J Nanotechnol Full Research Paper We perform molecular dynamics simulation on several relevant biological fibrils associated with neurodegenerative diseases such as Aβ(40), Aβ(42), and α-synuclein systems to obtain a molecular understanding and interpretation of nanomechanical characterization experiments. The computational method is versatile and addresses a new subarea within the mechanical characterization of heterogeneous soft materials. We investigate both the elastic and thermodynamic properties of the biological fibrils in order to substantiate experimental nanomechanical characterization techniques that are quickly developing and reaching dynamic imaging with video rate capabilities. The computational method qualitatively reproduces results of experiments with biological fibrils, validating its use in extrapolation to macroscopic material properties. Our computational techniques can be used for the co-design of new experiments aiming to unveil nanomechanical properties of biological fibrils from a point of view of molecular understanding. Our approach allows a comparison of diverse elastic properties based on different deformations , i.e., tensile (Y(L)), shear (S), and indentation (Y(T)) deformation. From our analysis, we find a significant elastic anisotropy between axial and transverse directions (i.e., Y(T) > Y(L)) for all systems. Interestingly, our results indicate a higher mechanostability of Aβ(42) fibrils compared to Aβ(40), suggesting a significant correlation between mechanical stability and aggregation propensity (rate) in amyloid systems. That is, the higher the mechanical stability the faster the fibril formation. Finally, we find that α-synuclein fibrils are thermally less stable than β-amyloid fibrils. We anticipate that our molecular-level analysis of the mechanical response under different deformation conditions for the range of fibrils considered here will provide significant insights for the experimental observations. Beilstein-Institut 2019-02-19 /pmc/articles/PMC6404408/ /pubmed/30873322 http://dx.doi.org/10.3762/bjnano.10.51 Text en Copyright © 2019, Poma et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms) |
spellingShingle | Full Research Paper Poma, Adolfo B Guzman, Horacio V Li, Mai Suan Theodorakis, Panagiotis E Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
title | Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
title_full | Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
title_fullStr | Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
title_full_unstemmed | Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
title_short | Mechanical and thermodynamic properties of Aβ(42), Aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
title_sort | mechanical and thermodynamic properties of aβ(42), aβ(40), and α-synuclein fibrils: a coarse-grained method to complement experimental studies |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404408/ https://www.ncbi.nlm.nih.gov/pubmed/30873322 http://dx.doi.org/10.3762/bjnano.10.51 |
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