Autonomous motors of a metal-organic framework powered by reorganization of self-assembled peptides at interfaces

被引:5
|
作者
Ikezoe, Yasuhiro [1 ]
Washino, Gosuke [2 ]
Uemura, Takashi [2 ]
Kitagawa, Susumu [2 ,3 ]
Matsui, Hiroshi [1 ]
机构
[1] CUNY Hunter Coll, Dept Chem & Biochem, New York, NY 10065 USA
[2] Kyoto Univ, Dept Synthet Chem & Biol Chem, Nishikyo Ku, Kyoto 6158510, Japan
[3] Kyoto Univ, Inst Integrated Cell Mat Sci WPI iCeMS, Sakyo Ku, Kyoto 6068501, Japan
基金
美国国家卫生研究院; 日本学术振兴会;
关键词
COORDINATION POLYMERS; DESIGN; POLYMERIZATION; SOLIDS; DRIVEN;
D O I
10.1038/NMAT3461
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A variety of microsystems have been developed that harness energy and convert it to mechanical motion. Here we have developed new autonomous biochemical motors by integrating a metal-organic framework (MOF) and self-assembling peptides. The MOF is applied as an energy-storing cell that assembles peptides inside nanoscale pores of the coordination framework. The nature of peptides enables their assemblies to be reconfigured at the water/MOF interface, and thus converted to fuel energy. Reorganization of hydrophobic peptides can create a large surface-tension gradient around the MOF that can efficiently power its translational motion. As a comparison, the velocity normalized by volume for the diphenylalanine-MOF particle is faster and the kinetic energy per unit mass of fuel is more than twice as great as that for previous gel motor systems. This demonstration opens the route towards new applications of MOFs and reconfigurable molecular self-assembly, possibly evolving into a smart autonomous motor capable of mimicking swimming bacteria and, with integrated recognition units, harvesting target chemicals.
引用
收藏
页码:1081 / 1085
页数:5
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