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

被引:28
作者
Poma, Adolfo B. [1 ]
Guzman, Horacio, V [2 ]
Mai Suan Li [3 ,4 ]
Theodorakis, Panagiotis E. [3 ]
机构
[1] Polish Acad Sci, Inst Fundamental Technol Res, Pawinskiego 5B, PL-02106 Warsaw, Poland
[2] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[3] Polish Acad Sci, Inst Phys, Al Lotnikow 32-46, PL-02668 Warsaw, Poland
[4] Quang Trung Software City, Inst Computat Sci & Technol, Dist 12, Ho Chi Minh City, Vietnam
关键词
beta-amyloid; atomic force microscopy; mechanical deformation; molecular simulation; proteins; alpha-synuclein; ATOMIC-FORCE MICROSCOPY; AMYLOID FIBRILS; CRYSTALLINE CELLULOSE; MOLECULAR-DYNAMICS; SINGLE PROTEIN; AGGREGATION; FIELD; FLEXIBILITY; ADHESION; CONTACT;
D O I
10.3762/bjnano.10.51
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We perform molecular dynamics simulation on several relevant biological fibrils associated with neurodegenerative diseases such as A beta(42), A beta(40), and a-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 A beta(42) fibrils compared to A 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 alpha-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.
引用
收藏
页码:500 / 513
页数:14
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