Evidence map›Paper›PMID 24551498›Full record

ArticleChemistryOpen2012

Synthesis and structural characterization of stable branched DNA g-quadruplexes using the trebler phosphoramidite.

Rubén Ferreira, Margarita Alvira, Anna Aviñó, Irene Gómez-Pinto, Carlos González, Valérie Gabelica, Ramon Eritja

Abstract read
In one paragraph

Article in ChemistryOpen, 2012. 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
–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

3 citing papers in PubMed.

  1. Synthesis of 2'-ACS omega · 2023
    Article
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  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

7 authors.

Rubén FerreiraDepartment of Chemical and Biomolecular Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), Networking Centre on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) Jordi Girona 18-26, 08034 Barcelona (Spain) ; Department of Chemistry and Molecular Pharmacology, Institute for Research in Biomedicine (IRB Barcelona) Baldiri i Reixac 10, 08028 Barcelona (Spain).
Margarita AlviraDepartment of Chemical and Biomolecular Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), Networking Centre on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) Jordi Girona 18-26, 08034 Barcelona (Spain) ; Department of Chemistry and Molecular Pharmacology, Institute for Research in Biomedicine (IRB Barcelona) Baldiri i Reixac 10, 08028 Barcelona (Spain).
Anna AviñóDepartment of Chemical and Biomolecular Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), Networking Centre on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) Jordi Girona 18-26, 08034 Barcelona (Spain) ; Department of Chemistry and Molecular Pharmacology, Institute for Research in Biomedicine (IRB Barcelona) Baldiri i Reixac 10, 08028 Barcelona (Spain).
Irene Gómez-PintoDepartmento de Química Física Biológica, Instituto de Química Física 'Rocasolano' CSIC, Serrano 119, 28006 Madrid (Spain).
Carlos GonzálezDepartmento de Química Física Biológica, Instituto de Química Física 'Rocasolano' CSIC, Serrano 119, 28006 Madrid (Spain).
Valérie GabelicaDepartment of Chemistry, University of Liège Allée de la Chimie Building B6c, 4000 Liège (Belgium).
Ramon EritjaDepartment of Chemical and Biomolecular Nanotechnology, Institute for Advanced Chemistry of Catalonia (IQAC-CSIC), Networking Centre on Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN) Jordi Girona 18-26, 08034 Barcelona (Spain) ; Department of Chemistry and Molecular Pharmacology, Institute for Research in Biomedicine (IRB Barcelona) Baldiri i Reixac 10, 08028 Barcelona (Spain).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guanine (G)-rich sequences can form a noncanonical four-stranded structure known as the G-quadruplex. G-quadruplex structures are interesting because of their potential biological properties and use in nanosciences. Here, we describe a method to prepare highly stable G-quadruplexes by linking four G-rich DNA strands to form a monomolecular G-quadruplex. In this method, one strand is synthesized first, and then a trebler molecule is added to simultaneously assemble the remaining three strands. This approach allows the introduction of specific modifications in only one of the strands. As a proof of concept, we prepared a quadruplex where one of the chains includes a change in polarity. A hybrid quadruplex is observed in ammonium acetate solutions, whereas in the presence of sodium or potassium, a parallel G-quadruplex structure is formed. In addition to the expected monomolecular quadruplexes, we observed the presence of dimeric G-quadruplex structures. We also applied the method to prepare G-quadruplexes containing a single 8-aminoguanine substitution and found that this single base stabilizes the G-quadruplex structure when located at an internal position.

Indexed as

8-aminoguaninesbranched oligonucleotidesDNA structuresG-quadruplexsoligonucleotides

Identifiers

PMID24551498
PMCPMC3922461

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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.