Evidence map›Paper›PMID 41394649›Full record

ArticlebioRxiv : the preprint server for biology2025

DNA Motors Powered by Exonuclease III for Autonomous Rolling Motion and Biosensing Applications.

Yusha Imtiaz, Joshua Hardin, Bakai Sheyitov, Luona Zhang, Alexander Foote, Mohamed Husaini Bin Abdul Rahman, Krista Jackson, Selma Piranej, Alisina Bazrafshan, Khalid Salaita

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

10 authors.

Yusha ImtiazDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0001-8997-6461
Joshua HardinDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0001-7470-9010
Bakai SheyitovDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.
Luona ZhangDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0003-1316-7734
Alexander FooteDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.
Mohamed Husaini Bin Abdul RahmanDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.
Krista JacksonDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.
Selma PiranejDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0002-1940-641X
Alisina BazrafshanDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.ORCID 0000-0002-3259-8196
Khalid SalaitaDepartment of Chemistry, Emory University, Atlanta, GA 30322, USA.

Funding

Rolosense: An innovative platform for automatic mobile phone readout of active SARS-CoV-2 particles (RADx-rad / SEED Administrative Supplement)U01AA029345 · NIAAA · EMORY UNIVERSITY · PI SALAITA, KHALID S. · 2021 to 2022
$1.4M
Biological Discovery through Chemical Innovation Training Program at Emory UniversityT32GM152344 · NIGMS · EMORY UNIVERSITY · PI Simon B. Blakey, ELLEN J. HESS · 2024 to 2026
$976k
NIAAA NIH HHS U01 AA029345NIGMS NIH HHS T32 GM152344
6 · The paper itself

Abstract

Nucleic acid-based synthetic motors emulate key behaviors of biological machines, enabling applications in biosensing and nanoscale actuation. Among the reported synthetic motors, RNase H-powered motors offer high speed and processivity with demonstrated applications in computation and viral sensing. However, these motors rely on RNA as "fuel" source, limiting their stability. Here, we report the development of a robust, RNA-free DNA motor powered by Exonuclease III. These motors exhibit self-avoiding rolling motion driven by enzymatic hydrolysis of surface-bound DNA fuel strands, consistent with a burnt-bridge Brownian ratchet mechanism of translocation. We systematically optimized motor performance by chemically tuning the fluorescence reporter, DNA sequence composition, and surface fuel density. Fluorescence and brightfield microscopy revealed super-diffusive and Lévy-like stop-and-go dynamics under optimized conditions. Importantly, the established DNA-only architecture confers resistance to RNase degradation, and the system can be configured for motion-based biosensing via aptamer-functionalized components that selectively stall in response to viral targets. Beyond the significance of creating a chemically stable, tunable, and biosensing-compatible DNA motor platform, the work also establishes the modularity of the rolling motor platform and highlights how enzymatic diversity can expand their chemical and functional scope.

Identifiers

PMID41394649
PMCPMC12697284

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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.