Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Poma, Adolfo B, Guzman, Horacio V, Li, Mai Suan, Theodorakis, Panagiotis E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
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
_version_ 1783400879048622080
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
work_keys_str_mv AT pomaadolfob mechanicalandthermodynamicpropertiesofab42ab40andasynucleinfibrilsacoarsegrainedmethodtocomplementexperimentalstudies
AT guzmanhoraciov mechanicalandthermodynamicpropertiesofab42ab40andasynucleinfibrilsacoarsegrainedmethodtocomplementexperimentalstudies
AT limaisuan mechanicalandthermodynamicpropertiesofab42ab40andasynucleinfibrilsacoarsegrainedmethodtocomplementexperimentalstudies
AT theodorakispanagiotise mechanicalandthermodynamicpropertiesofab42ab40andasynucleinfibrilsacoarsegrainedmethodtocomplementexperimentalstudies