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Antiviral mechanism of polyanionic carbosilane dendrimers against HIV-1

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13440%2F16%3A43887667" target="_blank" >RIV/44555601:13440/16:43887667 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.dovepress.com/antiviral-mechanism-of-polyanionic-carbosilane-dendrimers-against-hiv--peer-reviewed-fulltext-article-IJN" target="_blank" >https://www.dovepress.com/antiviral-mechanism-of-polyanionic-carbosilane-dendrimers-against-hiv--peer-reviewed-fulltext-article-IJN</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2147/IJN.S96352" target="_blank" >10.2147/IJN.S96352</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Antiviral mechanism of polyanionic carbosilane dendrimers against HIV-1

  • Original language description

    Nanotechnology-derived platforms, such as dendrimers, are very attractive in several biological applications. In the case of human immunodeficiency virus (HIV) infection, polyanionic carbosilane dendrimers have shown great potential as antiviral agents in the development of novel microbicides to prevent the sexual transmission of HIV-1. In this work, we studied the mechanism of two sulfated and naphthylsulfonated functionalized carbosilane dendrimers, G3-S16 and G2-NF16. They are able to inhibit viral infection at fusion and thus at the entry step. Both compounds impede the binding of viral particles to target cell surface and membrane fusion through the blockage of gp120-CD4 interaction. In addition, and for the first time, we demonstrate that dendrimers can inhibit cell-to-cell HIV transmission and difficult infectious synapse formation. Thus, carbosilane dendrimers' mode of action is a multifactorial process targeting several proteins from viral envelope and from host cells that could block HIV infection at different stages during the first step of infection.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    International Journal of Nanotechnology

  • ISSN

    1475-7435

  • e-ISSN

  • Volume of the periodical

    2016

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    14

  • Pages from-to

    1281-1294

  • UT code for WoS article

    000373327100001

  • EID of the result in the Scopus database