Evidence map›Paper›PMID 34204295›Full record

ArticleInternational journal of molecular sciences2021

Engineering of Janus-Like Dendrimers with Peptides Derived from Glycoproteins of Herpes Simplex Virus Type 1: Toward a Versatile and Novel Antiviral Platform.

Annarita Falanga, Valentina Del Genio, Elizabeth A Kaufman, Carla Zannella, Gianluigi Franci, Marcus Weck, Stefania Galdiero

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Selected strategies to fight pathogenic bacteria.Journal of enzyme inhibition and medicinal chemistry · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. An Overview of Supramolecular Platforms Boosting Drug Delivery.Bioinorganic chemistry and applications · 2023
    Review
  12. Article
  13. Review
  14. The Broad-Spectrum Antiviral Potential of the Amphibian Peptide AR-23.International journal of molecular sciences · 2022
    Article
  15. Article
  16. Antiviral Activity ofViruses · 2021
    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

7 authors at 5 institutions in 2 countries.

Annarita FalangaDepartment of Agricultural Sciences, University of Naples "Federico II", Via Università 100, Portici, 80055 Naples, Italy.ORCID 0000-0001-6538-8585
Valentina Del GenioDepartment of Pharmacy and CIRPEB, University of Naples "Federico II", Via Montesano 49, 80131 Naples, Italy.ORCID 0000-0003-4227-941X
Elizabeth A KaufmanDepartment of Chemistry and Molecular Design Institute, New York University, New York, NY 10003, USA.
Carla ZannellaDepartment of Experimental Medicine, Second University of Naples, Via de Crecchio 7, 80138 Naples, Italy.
Gianluigi FranciDepartment of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, 84081 Baronissi, Italy.ORCID 0000-0003-3321-4331
Marcus WeckDepartment of Chemistry and Molecular Design Institute, New York University, New York, NY 10003, USA.ORCID 0000-0002-6486-4268
Stefania GaldieroDepartment of Pharmacy and CIRPEB, University of Naples "Federico II", Via Montesano 49, 80131 Naples, Italy.ORCID 0000-0002-7849-7024
Centro Interuniversitario di Ricerca sui Peptidi Bioattivi · ITNew York University · USUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Naples Federico II · ITUniversity of Salerno · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Novel antiviral nanotherapeutics, which may inactivate the virus and block it from entering host cells, represent an important challenge to face viral global health emergencies around the world. Using a combination of bioorthogonal copper-catalyzed 1,3-dipolar alkyne/azide cycloaddition (CuAAC) and photoinitiated thiol-ene coupling, monofunctional and bifunctional peptidodendrimer conjugates were obtained. The conjugates are biocompatible and demonstrate no toxicity to cells at biologically relevant concentrations. Furthermore, the orthogonal addition of multiple copies of two different antiviral peptides on the surface of a single dendrimer allowed the resulting bioconjugates to inhibit Herpes simplex virus type 1 at both the early and the late stages of the infection process. The presented work builds on further improving this attractive design to obtain a new class of therapeutics.

Indexed as

GlycoproteinsHerpesvirus 1, HumanViral ProteinsAmino Acid SequenceAnimalsAntiviral AgentsCell LineCell SurvivalChemical PhenomenaChemistry Techniques, SyntheticCHO CellsChromatography, High Pressure LiquidCricetulusDendrimersMicrobial Sensitivity TestsMolecular StructureAntiviral AgentsDendrimersGlycoproteinsPeptidesViral Proteinsantiviral compoundsdendrimerspeptides

Identifiers

PMID34204295
PMCPMC8234430
OpenAlexW3169921644

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.