Robotic end-to-end fusion of microtubules powered by kinesin

被引:5
|
作者
Saper, Gadiel [1 ]
Tsitkov, Stanislav [1 ]
Katira, Parag [2 ]
Hess, Henry [1 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10032 USA
[2] San Diego State Univ, Dept Mech Engn, San Diego, CA 92182 USA
基金
美国国家科学基金会;
关键词
LENS-INDUCED CONFINEMENT; MOLECULAR ROBOTS; ACTIVE-TRANSPORT; DRIVEN; CAPTURE; LENGTH; SCALE;
D O I
10.1126/scirobotics.abj7200
中图分类号
TP24 [机器人技术];
学科分类号
080202 ; 1405 ;
摘要
The active assembly of molecules by nanorobots has advanced greatly since "molecular manufacturing"-that is, the use of nanoscale tools to build molecular structures-was proposed. In contrast to a catalyst, which acceler-ates a reaction by smoothing the potential energy surface along the reaction coordinate, molecular machines expend energy to accelerate a reaction relative to the baseline provided by thermal motion and forces. Here, we design a nanorobotics system to accelerate end-to-end microtubule assembly by using kinesin motors and a cir-cular confining chamber. We show that the mechanical interaction of kinesin-propelled microtubules gliding on a surface with the walls of the confining chamber results in a nonequilibrium distribution of microtubules, which increases the number of end-to-end microtubule fusion events 20-fold compared with microtubules gliding on a plane. In contrast to earlier nanorobots, where a nonequilibrium distribution was built into the initial state and drove the process, our nanorobotic system creates and actively maintains the building blocks in the concentrated state responsible for accelerated assembly through the adenosine triphosphate-fueled generation of force by kinesin-1 motor proteins. This approach can be used in the future to develop biohybrid or bioinspired nanorobots that use molecular machines to access nonequilibrium states and accelerate nanoscale assembly.
引用
收藏
页数:10
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