• search hit 9 of 44
Back to Result List

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.show moreshow less

Export metadata

Additional Services

Search Google Scholar Statistics
Metadaten
Author details: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
Title of parent work (English):ACS nano
Publisher:American Chemical Society
Place of publishing:Washington
Publication type:Article
Language:English
Date of first publication:2018/07/24
Publication year:2018
Release date:2021/11/15
Tag:click chemistry; heparan sulfate; herpes simplex virus; multivalent; nanoparticles; polyglycerol
Volume:12
Issue:7
Number of pages:14
First page:6429
Last Page:6442
Funding institution:DFGGerman Research Foundation (DFG) [AZ 97/3-2]; DRS-Honors Post-Doctoral Fellowship [2016-1]; [SFB 765]
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC classification:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer review:Referiert
Accept ✔
This website uses technically necessary session cookies. By continuing to use the website, you agree to this. You can find our privacy policy here.