Jiangsu Key Laboratory of Engineering Mechanics, School of Civil Engineering, Southeast University, Nanjing, JS, China; Department of Materials Science and Engineering, University of Washington, Roberts Hall, 333, Box 352120, Seattle, WA 98195-2120, USA.
Department of Materials Science and Engineering, University of Washington, Roberts Hall, 333, Box 352120, Seattle, WA 98195-2120, USA.
Acta Biomater. 2020 Apr 1;106:242-255. doi: 10.1016/j.actbio.2020.02.014. Epub 2020 Feb 19.
Among many dermal armors, fish scales have become a source of inspiration in the pursuit of "next-generation" structural materials. Although fish scales function in a hydrated environment, the role of water and intermolecular hydrogen bonding to their unique structural behavior has not been elucidated. Water molecules reside within and adjacent to the interpeptide locations of the collagen fibrils of the elasmodine and provide lubrication to the protein molecules during deformation. We evaluated the contributions of this lubrication and the intermolecular bonding to the mechanical behavior of elasmodine scales from the Black Carp (Mylopharyngodon piceus). Scales were exposed to polar solvents, followed by axial loading to failure and the deformation mechanisms were characterized via optical mechanics. Displacement of intermolecular water molecules by liquid polar solvents caused significant (p ≤ 0.05) increases in stiffness, strength and toughness of the scales. Removal of this lubrication decreased the capacity for non-linear deformation and toughness, which results from the increased resistance to fibril rotations and sliding caused by molecular friction. The intermolecular lubrication is a key component of the "protecto-flexibility" of scales and these natural armors as a system; it can serve as an important component of biomimetic-driven designs for flexible armor systems. STATEMENT OF SIGNIFICANCE: The natural armor of fish has become a topic of substantial scientific interest. Hydration is important to these materials as water molecules reside within the interpeptide locations of the collagen fibrils of the elasmodine and provide lubrication to the protein molecules during deformation. We explored the opportunity for tuning the mechanical behavior of scales as a model for next-generation engineering materials by adjusting the extent of hydrogen bonding with polar solvents and the corresponding interpeptide molecular lubrication. Removal of this lubrication decreased the capacity for non-linear deformation and toughness due to an increase in resistance to fibril rotations and sliding as imparted by molecular friction. We show that intermolecular lubrication is a key component of the "protecto-flexibility" of natural armors and it is an essential element of biomimetic approaches to develop flexible armor systems.
在众多的皮肤盔甲中,鱼鳞已经成为追求“下一代”结构材料的灵感来源。尽管鱼鳞在水合环境中发挥作用,但水和分子间氢键对其独特结构行为的作用尚未阐明。水分子存在于弹性蛋白的胶原纤维的肽间位置内和周围,并在变形过程中为蛋白质分子提供润滑。我们评估了这种润滑和分子间键合对来自黑鲤鱼(Mylopharyngodon piceus)的弹性蛋白鳞片的机械性能的贡献。鳞片暴露于极性溶剂中,然后进行轴向加载至失效,并通过光学力学对变形机制进行了表征。液态极性溶剂取代分子间的水分子会显著(p ≤ 0.05)增加鳞片的刚度、强度和韧性。这种润滑的去除降低了非线性变形和韧性的能力,这是由于分子摩擦导致纤维旋转和滑动的阻力增加所致。分子间润滑是鳞片“保护灵活性”的关键组成部分,也是作为一个系统的这些天然盔甲的关键组成部分;它可以作为仿生驱动设计灵活装甲系统的重要组成部分。
鱼类的天然盔甲已经成为一个重要的科学研究课题。水合作用对这些材料很重要,因为水分子存在于弹性蛋白的胶原纤维的肽间位置内,并在变形过程中为蛋白质分子提供润滑。我们通过用极性溶剂调整氢键的程度和相应的肽间分子润滑,探索了通过调整氢键的程度和相应的肽间分子润滑来调整鳞片机械性能的机会,作为下一代工程材料的模型。由于分子摩擦导致纤维旋转和滑动的阻力增加,这种润滑的去除降低了非线性变形和韧性的能力。我们表明,分子间润滑是天然盔甲“保护灵活性”的关键组成部分,是仿生方法开发灵活装甲系统的基本要素。