dc.contributor.author
Thongrom, Boonya
dc.contributor.author
Sharma, Antara
dc.contributor.author
Nie, Chuanxiong
dc.contributor.author
Quaas, Elisa
dc.contributor.author
Raue, Marwin
dc.contributor.author
Bhatia, Sumati
dc.contributor.author
Haag, Rainer
dc.date.accessioned
2022-05-16T06:02:14Z
dc.date.available
2022-05-16T06:02:14Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/35024
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-34740
dc.description.abstract
Herpes Simplex Virus-1 (HSV-1) with a diameter of 155–240 nm uses electrostatic interactions to bind with the heparan sulfate present on the cell surface to initiate infection. In this work, the initial contact using polysulfate-functionalized hydrogels is aimed to deter. The hydrogels provide a large contact surface area for viral interaction and sulfated hydrogels are good mimics for the native heparan sulfate. In this work, hydrogels of different flexibilities are synthesized, determined by rheology. Gels are prepared within an elastic modulus range of 10–1119 Pa with a mesh size of 80–15 nm, respectively. The virus binding studies carried out with the plaque assay show that the most flexible sulfated hydrogel performs the best in binding HSV viruses. These studies prove that polysulfated hydrogels are a viable option as HSV-1 antiviral compounds. Furthermore, such hydrogel networks are also physically similar to naturally occurring mucus gels and therefore may be used as mucus substitutes.
en
dc.format.extent
9 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
click chemistry
en
dc.subject
polysulfates
en
dc.subject
virus binding
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
Scaffold Flexibility Controls Binding of Herpes Simplex Virus Type 1 with Sulfated Dendritic Polyglycerol Hydrogels Fabricated by Thiol-Maleimide Click Reaction
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
2100507
dcterms.bibliographicCitation.doi
10.1002/mabi.202100507
dcterms.bibliographicCitation.journaltitle
Macromolecular Bioscience
dcterms.bibliographicCitation.number
5
dcterms.bibliographicCitation.volume
22
dcterms.bibliographicCitation.url
https://doi.org/10.1002/mabi.202100507
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie

refubium.funding
DEAL Wiley
refubium.note.author
Die Publikation wurde aus Open Access Publikationsgeldern der Freien Universität Berlin gefördert.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
1616-5195