Evidence map›Paper›PMID 26819321›Full record

ReviewMicrobiology and molecular biology reviews : MMBR2016

Biological Nanomotors with a Revolution, Linear, or Rotation Motion Mechanism.

Peixuan Guo, Hiroyuki Noji, Christopher M Yengo, Zhengyi Zhao, Ian Grainge

Open access · bronzeAbstract readReview
In one paragraph

Review in Microbiology and molecular biology reviews : MMBR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.8field-weighted citation impact, top 3% of its field
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

26 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Cryo-EM structure of cyanopodophage A4 reveals a pentameric pre-ejectosome in the double-stabilized capsid.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. A Catalysis-Driven Dual Molecular Motor.Journal of the American Chemical Society · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Computational modeling of protracted HCMV replication using genome substrates and protein temporal profiles.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Review
  11. FFrontiers in microbiology · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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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

5 authors at 5 institutions in 3 countries.

Peixuan GuoCollege of Pharmacy, The Ohio State University, Columbus, Ohio, USA Department of Physiology & Cell Biology, College of Medicine, The Ohio State University, Columbus, Ohio, USA Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, Columbus, Ohio, USA Nanobiotechnology Center, University of Kentucky, Lexington, Kentucky, USA Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, Kentucky, USA guo.1091@osu.edu.
Hiroyuki NojiDepartment of Applied Chemistry, The University of Tokyo, Tokyo, Japan.
Christopher M YengoDepartment of Cellular and Molecular Physiology, College of Medicine, Pennsylvania State University, Hershey, Pennsylvania, USA.
Zhengyi ZhaoCollege of Pharmacy, The Ohio State University, Columbus, Ohio, USA Department of Physiology & Cell Biology, College of Medicine, The Ohio State University, Columbus, Ohio, USA Dorothy M. Davis Heart and Lung Research Institute, The Ohio State University, Columbus, Ohio, USA Nanobiotechnology Center, University of Kentucky, Lexington, Kentucky, USA Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, Kentucky, USA.
Ian GraingeSchool of Environmental and Life Sciences, University of Newcastle, Callaghan, New South Wales, Australia.
Markey Cancer Center · USPennsylvania State University · USThe Ohio State University · USThe University of Tokyo · JPUniversity of Newcastle Australia · AU

Funding

Fruit exosome-like particles for therapeutic delivery of extracellular miRNAsUH3TR000875 · NCATS · UNIVERSITY OF LOUISVILLE · PI ZHANG, HUANG-GE · 2015 to 2017
$2.7M
Phi29 Motor Nanopore for Single Molecule Sensing and dsDNA FingerprintingR01EB012135 · NIBIB · UNIVERSITY OF KENTUCKY · PI GUO, PEIXUAN · 2011 to 2019
$2.6M
RNA Nanotechnology in Cancer TherapyU01CA151648 · NCI · UNIVERSITY OF KENTUCKY · PI GUO, PEIXUAN, LI, HENRY · 2010 to 2014
$2.1M
Cancer specific and organ-avoiding RNA architectures for quantitative imagingR01EB019036 · NIBIB · UNIVERSITY OF KENTUCKY · PI EVERS, BERNARD MARK, GUO, PEIXUAN · 2014 to 2017
$1.3M
Fruit exosome-like particles for therapeutic delivery of extracellular miRNAsUH2TR000875 · NCATS · UNIVERSITY OF LOUISVILLE · PI GUO, PEIXUAN, ZHANG, HUANG-GE · 2013 to 2014
$867k
NCATS NIH HHS TR000875NCATS NIH HHS UH2 TR000875NCATS NIH HHS UH3 TR000875NCI NIH HHS U01 CA151648NCI NIH HHS U01-CA151648NIBIB NIH HHS R01 EB012135NIBIB NIH HHS R01-EB012135NIBIB NIH HHS R01 EB019036NIBIB NIH HHS R01-EB019036
6 · The paper itself

Abstract

The ubiquitous biological nanomotors were classified into two categories in the past: linear and rotation motors. In 2013, a third type of biomotor, revolution without rotation (http://rnanano.osu.edu/movie.html), was discovered and found to be widespread among bacteria, eukaryotic viruses, and double-stranded DNA (dsDNA) bacteriophages. This review focuses on recent findings about various aspects of motors, including chirality, stoichiometry, channel size, entropy, conformational change, and energy usage rate, in a variety of well-studied motors, including FoF1 ATPase, helicases, viral dsDNA-packaging motors, bacterial chromosome translocases, myosin, kinesin, and dynein. In particular, dsDNA translocases are used to illustrate how these features relate to the motion mechanism and how nature elegantly evolved a revolution mechanism to avoid coiling and tangling during lengthy dsDNA genome transportation in cell division. Motor chirality and channel size are two factors that distinguish rotation motors from revolution motors. Rotation motors use right-handed channels to drive the right-handed dsDNA, similar to the way a nut drives the bolt with threads in same orientation; revolution motors use left-handed motor channels to revolve the right-handed dsDNA. Rotation motors use small channels (<2 nm in diameter) for the close contact of the channel wall with single-stranded DNA (ssDNA) or the 2-nm dsDNA bolt; revolution motors use larger channels (>3 nm) with room for the bolt to revolve. Binding and hydrolysis of ATP are linked to different conformational entropy changes in the motor that lead to altered affinity for the substrate and allow work to be done, for example, helicase unwinding of DNA or translocase directional movement of DNA.

Indexed as

AnimalsBacteriaBacterial ProteinsBacteriophagesDNA-Directed RNA PolymerasesDNA HelicasesDyneinsFlagellaGene ExpressionHumansKinesinsModels, MolecularMyosinsRotationViral ProteinsBacterial ProteinsDNA-Directed RNA PolymerasesDNA HelicasesDyneinsKinesinsMyosinsViral Proteins

Identifiers

PMID26819321
PMCPMC4771369
OpenAlexW2268601174

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.