Evidence map›Paper›PMID 27166371›Full record

ArticleNucleic acids research2016

Stabilization of i-motif structures by 2'-β-fluorination of DNA.

Hala Abou Assi, Robert W Harkness, Nerea Martin-Pintado, Christopher J Wilds, Ramón Campos-Olivas, Anthony K Mittermaier, Carlos González, Masad J Damha

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 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
4.2field-weighted citation impact, top 6% 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, 72 citations in OpenAlex.

  1. Article
  2. Review
  3. Enhanced i-Motif Stability through Consecutive 2',2'-Difluorocytidine Incorporation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  4. Article
  5. The Effect of 2'F-RNA on I-Motif Structure and Stability.Molecules (Basel, Switzerland) · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Crystal Structure of an i-Motif from the HRAS Oncogene Promoter.Angewandte Chemie (International ed. in English) · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. A DNA G-quadruplex/i-motif hybrid.Nucleic acids research · 2019
    Article
  20. Article
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

8 authors at 4 institutions in 2 countries.

Hala Abou AssiDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada.
Robert W HarknessDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada.
Nerea Martin-PintadoInstituto de Química Física 'Rocasolano', CSIC, 28006 Madrid, Spain.
Christopher J WildsDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada Department of Chemistry and Biochemistry, Concordia University, Montreal, QC H4B 1R6, Canada.
Ramón Campos-OlivasSpanish National Cancer Research Center (CNIO), 28029 Madrid, Spain.
Anthony K MittermaierDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada.
Carlos GonzálezInstituto de Química Física 'Rocasolano', CSIC, 28006 Madrid, Spain cgonzalez@iqfr.csic.es.
Masad J DamhaDepartment of Chemistry, McGill University, Montreal, QC H3A 0B8, Canada masad.damha@mcgill.ca.
McGill University · CAInstituto de Química Física Blas Cabrera · ESConcordia University · CASpanish National Cancer Research Centre · ES

Funding

CIHR
6 · The paper itself

Abstract

i-Motifs are four-stranded DNA structures consisting of two parallel DNA duplexes held together by hemi-protonated and intercalated cytosine base pairs (C:CH(+)). They have attracted considerable research interest for their potential role in gene regulation and their use as pH responsive switches and building blocks in macromolecular assemblies. At neutral and basic pH values, the cytosine bases deprotonate and the structure unfolds into single strands. To avoid this limitation and expand the range of environmental conditions supporting i-motif folding, we replaced the sugar in DNA by 2-deoxy-2-fluoroarabinose. We demonstrate that such a modification significantly stabilizes i-motif formation over a wide pH range, including pH 7. Nuclear magnetic resonance experiments reveal that 2-deoxy-2-fluoroarabinose adopts a C2'-endo conformation, instead of the C3'-endo conformation usually found in unmodified i-motifs. Nevertheless, this substitution does not alter the overall i-motif structure. This conformational change, together with the changes in charge distribution in the sugar caused by the electronegative fluorine atoms, leads to a number of favorable sequential and inter-strand electrostatic interactions. The availability of folded i-motifs at neutral pH will aid investigations into the biological function of i-motifs in vitro, and will expand i-motif applications in nanotechnology.

Indexed as

Base PairingNucleic Acid ConformationNucleotide MotifsCytosineDNAHydrogen-Ion ConcentrationIntercalating AgentsMagnetic Resonance SpectroscopyThermodynamicsCytosineDNAIntercalating Agents

Identifiers

PMID27166371
PMCPMC4914123
OpenAlexW2386898340

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.