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bioRxiv · 10.1101/527242

Mechanical and thermodynamic properties of Aβ42, Aβ40 and α-synuclein fibrils: A coarse-grained method to complement experimental studies

Poma, A.·Vargas Guzman, H. A.·Li, M. S.·Theodorakis, P.
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Abstract

We perform molecular dynamics simulation on several relevant biological fibrils associated with neurodegenerative diseases such as A{beta}40, A{beta}42, and the {beta}-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 molecular understanding point of view. Our approach allows a comparison of diverse elastic properties of the latter fibrils, which enables the detailed analysis of the mechanical response at the molecular level. For these systems, the simulation approach indicates qualitative agreement with the experimental estimations of the elastic moduli for three different types of deformation, i.e. tensile (YL), shear (S), and indentation (YT ). From our analysis, we find a significant elastic anisotropy between axial and transverse directions (i.e. YT>YL) for all systems. Interestingly, our results indicate a higher mechanostability in the case of A{beta}42 fibrils than in the case of {beta}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 -synuclein fibrils are thermally less stable than {beta}-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.

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Poma, A., Vargas Guzman, H. A., Li, M. S., Theodorakis, P.. 2019-01-22. Mechanical and thermodynamic properties of Aβ42, Aβ40 and α-synuclein fibrils: A coarse-grained method to complement experimental studies. https://doi.org/10.1101/527242

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