TY - JOUR
T1 - A nanoscale reciprocating rotary mechanism with coordinated mobility control
AU - Bertosin, Eva
AU - Maffeo, Christopher M.
AU - Drexler, Thomas
AU - Honemann, Maximilian N.
AU - Aksimentiev, Aleksei
AU - Dietz, Hendrik
N1 - This work was supported by a European Research Council Consolidator Grant to H.D. (GA no. 724261), the Deutsche Forschungsgemeinschaft through grants provided within the Gottfried-Wilhelm-Leibniz Program, and the SFB863 TPA9 Project ID 111166240 (to H.D.). A.A. and C.M.M. acknowledge support through National Science Foundation (USA) under grant DMR-1827346 and the National Institutes of Health under grant P41-GM104601 (to A.A.). Supercomputer time was provided through Leadership Resource Allocation MCB20012 on Frontera. We thank Massimo Kube and Dr. Fabian Kohler for helpful discussions on the cryo-EM reconstructions, Anna-Katharina Pumm and Dr. Wouter Engelen for support with the MATLAB script and the fluorescence microscopy experiments, and Alexander Koch for auxiliary experiments.
PY - 2021/12
Y1 - 2021/12
N2 - Biological molecular motors transform chemical energy into mechanical work by coupling cyclic catalytic reactions to large-scale structural transitions. Mechanical deformation can be surprisingly efficient in realizing such coupling, as demonstrated by the F1FO ATP synthase. Here, we describe a synthetic molecular mechanism that transforms a rotary motion of an asymmetric camshaft into reciprocating large-scale transitions in a surrounding stator orchestrated by mechanical deformation. We design the mechanism using DNA origami, characterize its structure via cryo-electron microscopy, and examine its dynamic behavior using single-particle fluorescence microscopy and molecular dynamics simulations. While the camshaft can rotate inside the stator by diffusion, the stator’s mechanics makes the camshaft pause at preferred orientations. By changing the stator’s mechanical stiffness, we accelerate or suppress the Brownian rotation, demonstrating an allosteric coupling between the camshaft and the stator. Our mechanism provides a framework for manufacturing artificial nanomachines that function because of coordinated movements of their components.
AB - Biological molecular motors transform chemical energy into mechanical work by coupling cyclic catalytic reactions to large-scale structural transitions. Mechanical deformation can be surprisingly efficient in realizing such coupling, as demonstrated by the F1FO ATP synthase. Here, we describe a synthetic molecular mechanism that transforms a rotary motion of an asymmetric camshaft into reciprocating large-scale transitions in a surrounding stator orchestrated by mechanical deformation. We design the mechanism using DNA origami, characterize its structure via cryo-electron microscopy, and examine its dynamic behavior using single-particle fluorescence microscopy and molecular dynamics simulations. While the camshaft can rotate inside the stator by diffusion, the stator’s mechanics makes the camshaft pause at preferred orientations. By changing the stator’s mechanical stiffness, we accelerate or suppress the Brownian rotation, demonstrating an allosteric coupling between the camshaft and the stator. Our mechanism provides a framework for manufacturing artificial nanomachines that function because of coordinated movements of their components.
UR - https://www.scopus.com/pages/publications/85120859665
UR - https://www.scopus.com/pages/publications/85120859665#tab=citedBy
U2 - 10.1038/s41467-021-27230-7
DO - 10.1038/s41467-021-27230-7
M3 - Article
C2 - 34880226
AN - SCOPUS:85120859665
SN - 2041-1723
VL - 12
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 7138
ER -