Evidence map›Paper›PMID 26382062›Full record

ArticlePloS one2015

Biomimetics: From Bioinformatics to Rational Design of Dendrimers as Gene Carriers.

Valeria Márquez-Miranda, María Belén Camarada, Ingrid Araya-Durán, Ignacio Varas-Concha, Daniel Eduardo Almonacid, Fernando Danilo González-Nilo

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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

6 authors.

Valeria Márquez-MirandaUniversidad Andres Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), Santiago, Chile; Fundación Fraunhofer Chile Research, Las Condes, Chile.
María Belén CamaradaUniversidad Bernardo O Higgins, Laboratorio de Bionanotecnología, Santiago, Chile.
Ingrid Araya-DuránUniversidad Andres Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), Santiago, Chile; Fundación Fraunhofer Chile Research, Las Condes, Chile.
Ignacio Varas-ConchaUniversidad Andres Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), Santiago, Chile.
Daniel Eduardo AlmonacidUniversidad Andres Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), Santiago, Chile; Centro Interdisciplinario de Neurociencia de Valparaíso, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso, Chile.
Fernando Danilo González-NiloUniversidad Andres Bello, Facultad de Biología, Center for Bioinformatics and Integrative Biology (CBIB), Santiago, Chile; Fundación Fraunhofer Chile Research, Las Condes, Chile; Centro Interdisciplinario de Neurociencia de Valparaíso, Facultad de Ciencias, Universidad de Valparaíso, Valparaíso, Chile.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biomimetics, or the use of principles of Nature for developing new materials, is a paradigm that could help Nanomedicine tremendously. One of the current challenges in Nanomedicine is the rational design of new efficient and safer gene carriers. Poly(amidoamine) (PAMAM) dendrimers are a well-known class of nanoparticles, extensively used as non-viral nucleic acid carriers, due to their positively charged end-groups. Yet, there are still several aspects that can be improved for their successful application in in vitro and in vivo systems, including their affinity for nucleic acids as well as lowering their cytotoxicity. In the search of new functional groups that could be used as new dendrimer-reactive groups, we followed a biomimetic approach to determine the amino acids with highest prevalence in protein-DNA interactions. Then we introduced them individually as terminal groups of dendrimers, generating a new class of nanoparticles. Molecular dynamics studies of two systems: PAMAM-Arg and PAMAM-Lys were also performed in order to describe the formation of complexes with DNA. Results confirmed that the introduction of amino acids as terminal groups in a dendrimer increases their affinity for DNA and the interactions in the complexes were characterized at atomic level. We end up by briefly discussing additional modifications that can be made to PAMAM dendrimers to turned them into promising new gene carriers.

Indexed as

BiomimeticsGene Transfer TechniquesNanoparticlesCell SurvivalDendrimersMolecular Dynamics SimulationDendrimersPAMAM Starburst

Identifiers

PMID26382062
PMCPMC4575034

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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.