Open this publication in new window or tab >>2018 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]
The most well-studied two-dimensional biomimetic cellular membrane modelsare self-assembled monolayers (SAMs) and supported lipid bilayers (SLBs).The former has the advantage of control over ligand density, homogeneity andorientation, allowing unambiguous interaction studies. It however lacks longrangelateral mobility, which is one of the most important aspects of cellularmembranes. SLBs are laterally mobile but they are fragile and instable uponexposure to air. Literature examples that contain all the above desirablecharacteristics with stimuli-responsiveness to fabricate biomaterials forbiosensing or modulating cell adhesion are rare. We here report on anadaptable platform, reversible self-assembled monolayers (rSAMs), featuringstrongly enhanced affinity towards influenza viruses as compared to SAMs,lateral mobility to investigate glycan-lectin interactions and tunable surfacedynamics to modulate cell adhesion. This new system utilizes noncovalentamidinium-carboxylate ion pairs for building up stable and ordered twodimensionalassemblies, akin to lipid bilayers but with a simple preparationprocess, stimuli-responsiveness and fast on/off rates.
Place, publisher, year, edition, pages
Malmö university, Faculty of Health and Society, 2018. p. 68
Series
Malmö University Health and Society Dissertations, ISSN 1653-5383 ; 7
Keywords
Lipid bilayers, Adaptable, Self-assembled, Monolayers, Supramolecular chemistry, Cell adhesion, Biocensor
National Category
Natural Sciences
Identifiers
urn:nbn:se:mau:diva-7321 (URN)10.24834/2043/24967 (DOI)24967 (Local ID)9789171049261 (ISBN)9789171049278 (ISBN)24967 (Archive number)24967 (OAI)
Note
Note: The papers are not included in the fulltext online.
Paper II and IV in dissertation as manuscript, paper II with title "pH-switchable lipid bilayer-like monolayers with ultrahigh lectin affinity", paper IV with title "Reversible self-assembled monolayers (rSAMs) with tunable surface dynamics modulate cell adhesion behaviour"
2020-02-282020-02-282024-03-18Bibliographically approved