折叠(DSP实现)
工作(物理)
蛋白质折叠
纳米技术
联轴节(管道)
机械化学
分子
材料科学
机械能
执行机构
蛋白质工程
生物物理学
分子机器
化学物理
化学
机械工程
物理
工程类
生物
电气工程
生物化学
热力学
功率(物理)
有机化学
酶
冶金
作者
Linglan Fu,Han Wang,Hongbin Li
出处
期刊:CCS Chemistry
[Chinese Chemical Society]
日期:2019-04-01
卷期号:1 (1): 138-147
被引量:50
标识
DOI:10.31635/ccschem.019.20180012
摘要
Mechanochemical coupling cycles underlie the work-generation mechanisms of biological systems and are realized by highly regulated conformational changes of the protein machineries. However, it has been challenging to utilize protein conformational changes to do mechanical work at the macroscopic level in biomaterials, and it remains elusive to construct macroscopic mechanochemical devices based on molecular-level mechanochemical coupling systems. Here, the authors demonstrate that protein folding can be utilized to realize protein’s mechanochemical cycles at both single-molecule and macroscopic levels. Our results demonstrate, for the first time, the successful harnessing of mechanical work generated by protein folding in a macroscopic protein hydrogel device, and the work generated by protein folding compares favorably with the energy output of molecular motors. Our work bridges a gap between single-molecule and macroscopic levels, and paves the way to utilizing proteins as building blocks to design protein-based artificial muscles and soft actuators.
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