Suppr超能文献

粗粒度模型中生物纤维的弹性模量:结晶纤维素和β-淀粉样蛋白。

Elastic moduli of biological fibers in a coarse-grained model: crystalline cellulose and β-amyloids.

作者信息

Poma Adolfo B, Chwastyk Mateusz, Cieplak Marek

机构信息

Institute of Physics, Polish Academy of Sciences, Aleja Lotników 32/46, PL-02668 Warsaw, Poland.

出版信息

Phys Chem Chem Phys. 2017 Oct 25;19(41):28195-28206. doi: 10.1039/c7cp05269c.

Abstract

We study the mechanical response of cellulose and β-amyloid microfibrils to three types of deformation: tensile, indentational, and shear. The cellulose microfibrils correspond to the allomorphs Iα or Iβ whereas the β-amyloid microfibrils correspond to the polymorphs of either two- or three-fold symmetry. This response can be characterized by three elastic moduli, namely, Y, Y, and S. We use a structure-based coarse-grained model to analyze the deformations in a unified manner. We find that each of the moduli is almost the same for the two allomorphs of cellulose but Y is about 20 times larger than Y (140 GPa vs. 7 GPa), indicating the existence of significant anisotropy. For cellulose we note that the anisotropy results from the involvement of covalent bonds in stretching. For β-amyloid, the sense of anisotropy is opposite to that of cellulose. In the three-fold symmetry case, Y is about half of Y (3 vs. 7) whereas for two-fold symmetry the anisotropy is much larger (1.6 vs. 21 GPa). The S modulus is derived to be 1.2 GPa for three-fold symmetry and one half of it for the other symmetry and 3.0 GPa for cellulose. The values of the moduli reflect deformations in the hydrogen-bond network. Unlike in our theoretical approach, no experiment can measure all three elastic moduli with the same apparatus. However, our theoretical results are consistent with various measured values: typical Y for cellulose Iβ ranges from 133 to 155 GPa, Y from 2 to 25 GPa, and S from 1.8 to 3.8 GPa. For β-amyloid, the experimental values of S and Y are about 0.3 GPa and 3.3 GPa respectively, while the value of Y has not been reported.

摘要

我们研究了纤维素和β-淀粉样微纤维对三种类型变形的力学响应:拉伸、压痕和剪切。纤维素微纤维对应于同质多晶型物Iα或Iβ,而β-淀粉样微纤维对应于具有二重或三重对称性的多晶型物。这种响应可以用三个弹性模量来表征,即Y、Y和S。我们使用基于结构的粗粒化模型以统一的方式分析变形。我们发现,纤维素的两种同质多晶型物的每个模量几乎相同,但Y比Y大约20倍(140吉帕斯卡对7吉帕斯卡),表明存在显著的各向异性。对于纤维素,我们注意到各向异性是由于共价键参与拉伸所致。对于β-淀粉样蛋白,各向异性的方向与纤维素相反。在三重对称情况下,Y约为Y的一半(3对7),而在二重对称情况下,各向异性要大得多(1.6对21吉帕斯卡)。对于三重对称,S模量推导为1.2吉帕斯卡,对于另一种对称则为其一半,对于纤维素为3.0吉帕斯卡。模量值反映了氢键网络中的变形。与我们的理论方法不同,没有实验能够用同一仪器测量所有三个弹性模量。然而,我们的理论结果与各种测量值一致:纤维素Iβ的典型Y值范围为133至155吉帕斯卡,Y值为2至25吉帕斯卡,S值为1.8至3.8吉帕斯卡。对于β-淀粉样蛋白,S和Y的实验值分别约为0.3吉帕斯卡和3.3吉帕斯卡,而Y值尚未报道。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验