In Situ Monitoring of Linear RGD-Peptide Bioconjugation with Nanoscale Polymer Brushes

dc.bibliographicCitation.firstPage946
dc.bibliographicCitation.issue3
dc.bibliographicCitation.journalTitleACS omegaeng
dc.bibliographicCitation.lastPage958
dc.bibliographicCitation.volume2
dc.contributor.authorPsarra, Evmorfia
dc.contributor.authorKönig, Ulla
dc.contributor.authorMüller, Martin
dc.contributor.authorBittrich, Eva
dc.contributor.authorEichhorn, Klaus-Jochen
dc.contributor.authorWelzel, Petra B.
dc.contributor.authorStamm, Manfred
dc.contributor.authorUhlmann, Petra
dc.date.accessioned2023-02-27T08:51:28Z
dc.date.available2023-02-27T08:51:28Z
dc.date.issued2017
dc.description.abstractBioinspired materials mimicking the native extracellular matrix environment are promising for biotechnological applications. Particularly, modular biosurface engineering based on the functionalization of stimuli-responsive polymer brushes with peptide sequences can be used for the development of smart surfaces with biomimetic cues. The key aspect of this study is the in situ monitoring and analytical verification of the biofunctionalization process on the basis of three complementary analytical techniques. In situ spectroscopic ellipsometry was used to quantify the amount of chemisorbed GRGDS at both the homopolymer poly(acrylic acid) (PAA) brush and the binary poly(N-isopropylacrylamide) (PNIPAAm)-PAA brushes, which was finally confirmed by an acidic hydrolysis combined with a subsequent reverse-phase high-performance liquid chromatography analysis. In situ attenuated total reflection-Fourier transform infrared spectroscopy provided a step-by-step detection of the biofunctionalization process so that an optimized protocol for the bioconjugation of GRGDS could be identified. The optimized protocol was used to create a temperature-responsive binary brush with a high amount of chemisorbed GRGDS, which is a promising candidate for the temperature-sensitive control of GRGDS presentation in further cell-instructive studies.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/11518
dc.identifier.urihttp://dx.doi.org/10.34657/10552
dc.language.isoeng
dc.publisherWashington, DC : ACS Publications
dc.relation.doihttps://doi.org/10.1021/acsomega.6b00450
dc.relation.essn2470-1343
dc.rights.licenseACS AuthorChoice
dc.rights.urihttps://pubs.acs.org/page/policy/authorchoice_termsofuse.html
dc.subject.ddc540
dc.subject.ddc660
dc.subject.otherbovine serum-albumineng
dc.subject.otherprotein adsorptioneng
dc.subject.othercell-adhesioneng
dc.subject.othernanomechanical propertieseng
dc.subject.otherpolyelectrolyte brusheseng
dc.subject.otheratr-ftireng
dc.subject.othersurfaceeng
dc.subject.othercarbodiimideeng
dc.subject.otherbindingeng
dc.subject.otheracideng
dc.titleIn Situ Monitoring of Linear RGD-Peptide Bioconjugation with Nanoscale Polymer Brusheseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorIPF
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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