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dc.contributor.authorSchirmer, Johanna
dc.contributor.authorIatta, Ester
dc.contributor.authorEmelianov, Aleksei V.
dc.contributor.authorNissinen, Maija
dc.contributor.authorPettersson, Mika
dc.date.accessioned2024-01-02T08:08:23Z
dc.date.available2024-01-02T08:08:23Z
dc.date.issued2023
dc.identifier.citationSchirmer, J., Iatta, E., Emelianov, A. V., Nissinen, M., & Pettersson, M. (2023). Catalytic Activity of Horseradish Peroxidase Immobilized on Pristine and Two‐Photon Oxidized Graphene. <i>Advanced Materials Interfaces</i>, <i>Early View</i>, Article 2300870. <a href="https://doi.org/10.1002/admi.202300870" target="_blank">https://doi.org/10.1002/admi.202300870</a>
dc.identifier.otherCONVID_197240931
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/92521
dc.description.abstractBiosensors based on graphene and bio-graphene interfaces have gained momentum in recent years due to graphene's outstanding electronic and mechanical properties. By introducing the patterning of a single-layer graphene surface by two-photon oxidation (2PO), the surface hydrophobicity/hydrophilicity and doping can be varied at the nanoscale while preserving the carbon network, thus opening possibilities to design new devices. In this study, the effect of 2PO on the catalytic activity of the noncovalently immobilized enzyme horseradish peroxidase (HRP) on single-layer graphene-coated Si/SiO2 chips is presented. To monitor the activity continuously, a simple well-plate setup is introduced. Upon controllable 1–2-layer immobilization, the catalytic activity decreases to a maximum value of 7.5% of the free enzyme. Interestingly, the activity decreases with increasing 2PO area on the samples. Hence, the HRP catalytic activity on the graphene surface is locally controlled. This approach can enable the development of graphene-bio interfaces with locally varying enzyme activity.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesAdvanced Materials Interfaces
dc.rightsCC BY 4.0
dc.titleCatalytic Activity of Horseradish Peroxidase Immobilized on Pristine and Two‐Photon Oxidized Graphene
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202401021025
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineFysikaalinen kemiafi
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centeren
dc.contributor.oppiainePhysical Chemistryen
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2196-7350
dc.relation.volumeEarly View
dc.type.versionpublishedVersion
dc.rights.copyright© 2023 The Authors.
dc.rights.accesslevelopenAccessfi
dc.subject.ysoperoksidaasit
dc.subject.ysokatalyysi
dc.subject.ysografeeni
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p21810
jyx.subject.urihttp://www.yso.fi/onto/yso/p8704
jyx.subject.urihttp://www.yso.fi/onto/yso/p24483
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1002/admi.202300870
jyx.fundinginformationThis work was funded by Jane and Aatos Erkko Foundation. The authors would like to thank Jane and Aatos Erkko Foundation for supporting the work, Olli Rissanen for the production of the graphene samples, and Dr. Pasi Myllyperkiö for the design and development of the oxidation laser setup.
dc.type.okmA1


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