Versatile multi-functionalization of protein nanofibrils for biosensor applications

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dc.contributor.author Sasso, L en
dc.contributor.author Suei, S en
dc.contributor.author Domigan, Laura en
dc.contributor.author Healy, J en
dc.contributor.author Nock, V en
dc.contributor.author Williams, MAK en
dc.contributor.author Gerrard, Juliet en
dc.date.accessioned 2017-08-14T21:56:22Z en
dc.date.available 2013-11-15 en
dc.date.issued 2014 en
dc.identifier.citation Nanoscale, 6(3):1629-1634 2014 en
dc.identifier.issn 2040-3364 en
dc.identifier.uri http://hdl.handle.net/2292/35083 en
dc.description.abstract Protein nanofibrils offer advantages over other nanostructures due to the ease in their self-assembly and the versatility of surface chemistry available. Yet, an efficient and general methodology for their post-assembly functionalization remains a significant challenge. We introduce a generic approach, based on biotinylation and thiolation, for the multi-functionalization of protein nanofibrils self-assembled from whey proteins. Biochemical characterization shows the effects of the functionalization onto the nanofibrils' surface, giving insights into the changes in surface chemistry of the nanostructures. We show how these methods can be used to decorate whey protein nanofibrils with several components such as fluorescent quantum dots, enzymes, and metal nanoparticles. A multi-functionalization approach is used, as a proof of principle, for the development of a glucose biosensor platform, where the protein nanofibrils act as nanoscaffolds for glucose oxidase. Biotinylation is used for enzyme attachment and thiolation for nanoscaffold anchoring onto a gold electrode surface. Characterization via cyclic voltammetry shows an increase in glucose-oxidase mediated current response due to thiol-metal interactions with the gold electrode. The presented approach for protein nanofibril multi-functionalization is novel and has the potential of being applied to other protein nanostructures with similar surface chemistry. en
dc.description.uri https://www.ncbi.nlm.nih.gov/pubmed/24337159 en
dc.format.medium Print en
dc.language English en
dc.publisher Royal Society of Chemistry en
dc.relation.ispartofseries Nanoscale en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://sherpa.ac.uk/romeo/issn/2040-3364/ http://www.rsc.org/journals-books-databases/open-access/green-open-access/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject Gold en
dc.subject Amines en
dc.subject Sulfhydryl Compounds en
dc.subject Biotin en
dc.subject Glucose Oxidase en
dc.subject Glucose en
dc.subject Streptavidin en
dc.subject Milk Proteins en
dc.subject Cross-Linking Reagents en
dc.subject Microscopy, Electron, Transmission en
dc.subject Microscopy, Atomic Force en
dc.subject Biotinylation en
dc.subject Biosensing Techniques en
dc.subject Electrodes en
dc.subject Quantum Dots en
dc.subject Electrochemistry en
dc.subject Surface Properties en
dc.subject Nanotechnology en
dc.subject Metal Nanoparticles en
dc.title Versatile multi-functionalization of protein nanofibrils for biosensor applications en
dc.type Journal Article en
dc.identifier.doi 10.1039/c3nr05752f en
pubs.issue 3 en
pubs.begin-page 1629 en
pubs.volume 6 en
dc.rights.holder Copyright: Royal Society of Chemistry en
dc.identifier.pmid 24337159 en
pubs.author-url http://pubs.rsc.org/en/Content/ArticleLanding/2014/NR/C3NR05752F en
pubs.end-page 1634 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 457327 en
pubs.org-id Engineering en
pubs.org-id Chemical and Materials Eng en
pubs.org-id Science en
pubs.org-id Biological Sciences en
dc.identifier.eissn 2040-3372 en
pubs.record-created-at-source-date 2017-08-15 en
pubs.dimensions-id 24337159 en


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