Evidence map›Paper›PMID 41741468›Full record

ArticleNature communications2026

A tunable autonomous RNA-fueled micro-engine.

Kun Wang, Wenjun Chen, Buming Guo, Qiuyan Huang, Guolong Zhu, Heng Ni, Lei Zhang, Melanie Perez, Ruojie Sha, Nadrian C Seeman and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Kun WangDepartment of Physics, New York University, New York, NY, USA. kunwangneu@gmail.com.ORCID http://orcid.org/0000-0002-7099-0367
Wenjun ChenDepartment of Physics, New York University, New York, NY, USA.
Buming GuoDepartment of Physics, New York University, New York, NY, USA.ORCID http://orcid.org/0000-0003-2581-7933
Qiuyan HuangDepartment of Chemistry, New York University, New York, NY, USA.
Guolong ZhuDepartment of Chemistry, Biochemistry and Physics, Fairleigh Dickinson University, Madison, NJ, USA.ORCID http://orcid.org/0000-0001-8893-5617
Heng NiDepartment of Physics, New York University, New York, NY, USA.
Lei ZhangDepartment of Physics, New York University, New York, NY, USA.
Melanie PerezDepartment of Chemistry, Biochemistry and Physics, Fairleigh Dickinson University, Madison, NJ, USA.
Ruojie ShaDepartment of Chemistry, New York University, New York, NY, USA.ORCID http://orcid.org/0000-0002-0807-734X
Nadrian C SeemanDepartment of Chemistry, New York University, New York, NY, USA.ORCID http://orcid.org/0000-0002-9680-4649
Paul M ChaikinDepartment of Physics, New York University, New York, NY, USA. chaikin@nyu.edu.ORCID http://orcid.org/0000-0001-9864-0089

Funding

National Science Foundation (NSF) CCF-2106790National Science Foundation (NSF) No. 1504867Simons Foundation No. 7200138United States Department of Defense | United States Navy | Office of Naval Research (ONR) N000141912596U.S. Department of Energy (DOE) DE-SC0000989U.S. Department of Energy (DOE) DE-SC0007991
6 · The paper itself

Abstract

Autonomous molecular machines capable of converting chemical energy into mechanical motion are foundational components for synthetic nanoscale systems. Inspired by biological motors, we report the construction of a tunable, RNA-fueled DNA origami engine that drives the cyclic movement of a 500 nm-diameter particle at the microscale. The engine operates via sequential RNA-DNA hybridization and enzymatic cleavage by RNase H, enabling reversible switching between folded and unfolded conformations without external intervention. By modulating RNA and enzyme concentrations and controlling temperature, we achieve tunable switching kinetics, with transition periods as short as ~10 s. Kinetic modeling reveals that the folding pathway is governed by both productive RNA binding and the enzymatic clearance of misfolded intermediates, while unfolding is primarily controlled by RNase H activity. Since the RNA fuel binds specifically to the DNA strands, each engine is addressable simply by changing the sequences. This work demonstrates a programmable, self-resetting molecular actuator and offers a blueprint for building more complex nanomechanical systems with forces and energies comparable to molecular motors.

Indexed as

DNARNADNA NanostructuresKineticsNanotechnologyNucleic Acid ConformationNucleic Acid HybridizationRibonuclease HTemperatureDNARibonuclease HRNA

Identifiers

PMID41741468
PMCPMC13046739

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.