Evidence map›Paper›PMID 23901273›Full record

ArticleInternational journal of nanomedicine2013

gH625 is a viral derived peptide for effective delivery of intrinsically disordered proteins.

Giovanni Smaldone, Annarita Falanga, Domenica Capasso, Daniela Guarnieri, Stefania Correale, Massimiliano Galdiero, Paolo A Netti, Massimo Zollo, Stefania Galdiero, Sonia Di Gaetano and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Functionalized Platinum Nanoparticles with Biomedical Applications.International journal of molecular sciences · 2022
    Review
  2. Article
  3. RNAi therapeutic strategies for acute respiratory distress syndrome.Translational research : the journal of laboratory and clinical medicine · 2019
    Review
  4. Review
  5. Review
  6. Article
  7. Membranotropic Cell Penetrating Peptides: The Outstanding Journey.International journal of molecular sciences · 2015
    Review
  8. Article
  9. Article
  10. Review
  11. Exploitation of viral properties for intracellular delivery.Journal of peptide science : an official publication of the European Peptide Society · 2014
    Review
  12. Article
  13. Peptide-lipid interactions: experiments and applications.International journal of molecular sciences · 2013
    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

11 authors at 4 institutions in 1 country.

Giovanni SmaldoneInstitute of Biostructures and Bioimaging, National Research Council, Naples, Italy.
Annarita Falanga
Domenica Capasso
Daniela Guarnieri
Stefania Correale
Massimiliano Galdiero
Paolo A Netti
Massimo Zollo
Stefania Galdiero
Sonia Di Gaetano
Emilia Pedone
Institute of Biostructure and Bioimaging · ITUniversity of Naples Federico II · ITCeinge Biotecnologie Avanzate (Italy) · ITItalian Institute of Technology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A genetically modified recombinant gH625-c-prune was prepared through conjugation of c-prune with gH625, a peptide encompassing 625-644 residues of the glycoprotein H of herpes simplex virus 1, which has been proved to possess the ability to carry cargo molecules across cell membranes. C-prune is the C-terminal domain of h-prune, overexpressed in breast, colorectal, and gastric cancers, interacting with multiple partners, and representing an ideal target for inhibition of cancer development. Its C-terminal domain results in an intrinsically disordered domain (IDD), and the peculiar properties of gH625 render it an optimal candidate to act as a carrier for this net negatively charged molecule by comparison with the positively charged TAT. A characterization of the recombinant gH625-c-prune fusion protein was conducted by biochemical, cellular biology and confocal microscopy means in comparison with TAT-c-prune. The results showed that the gH625-c-prune exhibited the ability to cross biomembranes, opening a new scenario on the use of gH625 as a novel multifunctional carrier.

Indexed as

Carrier ProteinsCircular DichroismDrug CarriersEndocytosisHeLa CellsHumansIntrinsically Disordered ProteinsNeoplasm ProteinsPeptidesPhosphoric Monoester HydrolasesProtein Structure, TertiaryRecombinant Fusion ProteinsViral Envelope ProteinsCarrier ProteinsDrug Carriersglycoprotein H, herpes simplex virus type 1Intrinsically Disordered ProteinsNeoplasm ProteinsPeptidesPhosphoric Monoester HydrolasesPRUNE1 protein, humanRecombinant Fusion ProteinsViral Envelope ProteinsdeliveryIDP

Identifiers

PMID23901273
PMCPMC3726435
OpenAlexW2053326583

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.