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Multivalent flexible nanogels exhibit broad-spectrum antiviral activity by blocking virus entry

  • The entry process of viruses into host cells is complex and involves stable but transient multivalent interactions with different cell surface receptors. The initial contact of several viruses begins with attachment to heparan sulfate (HS) proteoglycans on the cell surface, which results in a cascade of events that end up with virus entry. The development of antiviral agents based on multivalent interactions to shield virus particles and block initial interactions with cellular receptors has attracted attention in antiviral research. Here, we designed nanogels with different degrees of flexibility based on dendritic polyglycerol sulfate to mimic cellular HS. The designed nanogels are nontoxic and broad-spectrum, can multivalently interact with viral glycoproteins, shield virus surfaces, and efficiently block infection. We also visualized virus-nanogel interactions as well as the uptake of nanogels by the cells through clathrin-mediated endocytosis using confocal microscopy. As many human viruses attach to the cells through HSThe entry process of viruses into host cells is complex and involves stable but transient multivalent interactions with different cell surface receptors. The initial contact of several viruses begins with attachment to heparan sulfate (HS) proteoglycans on the cell surface, which results in a cascade of events that end up with virus entry. The development of antiviral agents based on multivalent interactions to shield virus particles and block initial interactions with cellular receptors has attracted attention in antiviral research. Here, we designed nanogels with different degrees of flexibility based on dendritic polyglycerol sulfate to mimic cellular HS. The designed nanogels are nontoxic and broad-spectrum, can multivalently interact with viral glycoproteins, shield virus surfaces, and efficiently block infection. We also visualized virus-nanogel interactions as well as the uptake of nanogels by the cells through clathrin-mediated endocytosis using confocal microscopy. As many human viruses attach to the cells through HS moieties, we introduce our flexible nanogels as robust inhibitors for these viruses.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Pradip DeyORCiD, Tobias BergmannGND, Jose Luis Cuellar-Camacho, Svenja EhrmannORCiD, Mohammad Suman Chowdhury, Minze Zhang, Ismail Dahmani, Rainer Haag, Walid AzadORCiD
DOI:https://doi.org/10.1021/acsnano.8b01616
ISSN:1936-0851
ISSN:1936-086X
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/29894156
Titel des übergeordneten Werks (Englisch):ACS nano
Verlag:American Chemical Society
Verlagsort:Washington
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:24.07.2018
Erscheinungsjahr:2018
Datum der Freischaltung:15.11.2021
Freies Schlagwort / Tag:click chemistry; heparan sulfate; herpes simplex virus; multivalent; nanoparticles; polyglycerol
Band:12
Ausgabe:7
Seitenanzahl:14
Erste Seite:6429
Letzte Seite:6442
Fördernde Institution:DFGGerman Research Foundation (DFG) [AZ 97/3-2]; DRS-Honors Post-Doctoral Fellowship [2016-1]; [SFB 765]
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
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