Evidence map›Paper›PMID 29517086›Full record

ArticleNanoscale2018

Dynamic self-assembly of DNA minor groove-binding ligand DB921 into nanotubes triggered by an alkali halide.

R Mizuta, J M Devos, J Webster, W L Ling, T Narayanan, A Round, D Munnur, E Mossou, A A Farahat, D W Boykin and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Nanoscale, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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

17 authors at 7 institutions in 4 countries.

R MizutaInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France and European Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38000 Grenoble, France. mitchell@esrf.eu.
J M DevosInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France.
J WebsterInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France and European Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38000 Grenoble, France. mitchell@esrf.eu.ORCID http://orcid.org/0000-0002-2264-5833
W L LingUniv. Grenoble Alpes, CEA, CNRS, IBS, F-38000 Grenoble, France.ORCID http://orcid.org/0000-0002-0574-7248
T NarayananEuropean Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38000 Grenoble, France. mitchell@esrf.eu.ORCID http://orcid.org/0000-0003-1957-1041
A RoundEuropean Molecular Biology Laboratory, 71 Avenue des Martyrs, 38000 Grenoble, France and Faculty of Natural Sciences, Keele University, Staffordshire, ST5 5BG, UK.ORCID http://orcid.org/0000-0002-0723-8228
D MunnurInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France and European Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38000 Grenoble, France. mitchell@esrf.eu and School of Pharmacy, University College London, Brunswick Square, London, WC1N 1AX, UK.
E MossouInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France and Faculty of Natural Sciences, Keele University, Staffordshire, ST5 5BG, UK.
A A FarahatDepartment of Chemistry, Georgia State University, Atlanta, GA 30303, USA and Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.ORCID http://orcid.org/0000-0003-0664-5670
D W BoykinDepartment of Chemistry, Georgia State University, Atlanta, GA 30303, USA.ORCID http://orcid.org/0000-0001-9712-8278
W D WilsonDepartment of Chemistry, Georgia State University, Atlanta, GA 30303, USA.ORCID http://orcid.org/0000-0001-5225-5089
S NeidleSchool of Pharmacy, University College London, Brunswick Square, London, WC1N 1AX, UK.ORCID http://orcid.org/0000-0003-0622-6548
R SchweinsInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France.ORCID http://orcid.org/0000-0001-8078-2089
P RannouUniv. Grenoble Alpes, CNRS, CEA, INAC-SyMMES, 38000 Grenoble, France.ORCID http://orcid.org/0000-0001-9376-7136
M HaertleinInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France.
V T ForsythInstitut Laue-Langevin, 71 Avenue des Martyrs, 38000 Grenoble, France and Faculty of Natural Sciences, Keele University, Staffordshire, ST5 5BG, UK.ORCID http://orcid.org/0000-0003-0380-3477
E P MitchellEuropean Synchrotron Radiation Facility, 71 Avenue des Martyrs, 38000 Grenoble, France. mitchell@esrf.eu and Faculty of Natural Sciences, Keele University, Staffordshire, ST5 5BG, UK.ORCID http://orcid.org/0000-0001-9809-9536
European Synchrotron Radiation Facility · FRInstitut Laue-Langevin · FRCentre National de la Recherche Scientifique · FRGeorgia State University · USEuropean Molecular Biology Laboratory · FRMansoura University · EGTransnational Press London

Funding

Molecular Design for Specific Recognition of Functional DNA SequencesR01GM111749 · NIGMS · GEORGIA STATE UNIVERSITY · PI WILSON, W DAVID · 2014 to 2021
$2.5M
NIGMS NIH HHS R01 GM111749
6 · The paper itself

Abstract

We describe a novel self-assembling supramolecular nanotube system formed by a heterocyclic cationic molecule which was originally designed for its potential as an antiparasitic and DNA sequence recognition agent. Our structural characterisation work indicates that the nanotubes form via a hierarchical assembly mechanism that can be triggered and tuned by well-defined concentrations of simple alkali halide salts in water. The nanotubes assembled in NaCl have inner and outer diameters of ca. 22 nm and 26 nm respectively, with lengths that reach into several microns. Our results suggest the tubes consist of DB921 molecules stacked along the direction of the nanotube long axis. The tubes are stabilised by face-to-face π-π stacking and ionic interactions between the charged amidinium groups of the ligand and the negative halide ions. The assembly process of the nanotubes was followed using small-angle X-ray and neutron scattering, transmission electron microscopy and ultraviolet/visible spectroscopy. Our data demonstrate that assembly occurs through the formation of intermediate ribbon-like structures that in turn form helices that tighten and compact to form the final stable filament. This assembly process was tested using different alkali-metal salts, showing a strong preference for chloride or bromide anions and with little dependency on the type of cation. Our data further demonstrates the existence of a critical anion concentration above which the rate of self-assembly is greatly enhanced.

Indexed as

AlkaliesAmidinesBenzimidazolesDNAHalogensLigandsNanotubesAlkaliesAmidinesBenzimidazolesDB 921DNAHalogensLigands

Identifiers

PMID29517086
PMCPMC5885265
OpenAlexW2794414857

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.