Avinash M B, Raut Devaraj, Mishra Manish Kumar, Ramamurty Upadrasta, Govindaraju T
Bioorganic Chemistry Laboratory, New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur P. O., Bengaluru 560064, India.
Department of Materials Engineering, Indian Institute of Science, Bengaluru 560012, India.
Sci Rep. 2015 Nov 3;5:16070. doi: 10.1038/srep16070.
A simple solution-processing and self-assembly approach that exploits the synergistic interactions between multiple hydrogen bonded networks and aromatic interactions was utilized to synthesize molecular crystals of cyclic dipeptides (CDPs), whose molecular weights (~0.2 kDa) are nearly three orders of magnitude smaller than that of natural structural proteins (50-300 kDa). Mechanical properties of these materials, measured using the nanoindentation technique, indicate that the stiffness and strength are comparable and sometimes better than those of natural fibres. The measured mechanical responses were rationalized by recourse to the crystallographic structural analysis and intermolecular interactions in the self-assembled single crystals. With this work we highlight the significance of developing small molecule based bioinspired design strategies to emulate biomechanical properties. A particular advantage of the successfully demonstrated reductionistic strategy of the present work is its amenability for realistic industrial scale manufacturing of designer biomaterials with desired mechanical properties.
一种利用多个氢键网络与芳香相互作用之间的协同作用的简单溶液处理和自组装方法被用于合成环状二肽(CDP)的分子晶体,其分子量(约0.2 kDa)比天然结构蛋白(50 - 300 kDa)小近三个数量级。使用纳米压痕技术测量这些材料的力学性能,结果表明其刚度和强度相当,有时甚至优于天然纤维。通过对自组装单晶的晶体结构分析和分子间相互作用,对测得的力学响应进行了合理的解释。通过这项工作,我们强调了开发基于小分子的仿生设计策略以模拟生物力学性能的重要性。本工作成功展示的还原策略的一个特别优势在于,它适合以实际工业规模制造具有所需力学性能的定制生物材料。