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Molecularly imprinted electropolymer for a hexameric heme protein with direct electron transfer and peroxide electrocatalysis

  • For the first time a molecularly imprinted polymer (MIP) with direct electron transfer (DET) and bioelectrocatalytic activity of the target protein is presented. Thin films of MIPs for the recognition of a hexameric tyrosine-coordinated heme protein (HTHP) have been prepared by electropolymerization of scopoletin after oriented assembly of HTHP on a self-assembled monolayer (SAM) of mercaptoundecanoic acid (MUA) on gold electrodes. Cavities which should resemble the shape and size of HTHP were formed by template removal. Rebinding of the target protein sums up the recognition by non-covalent interactions between the protein and the MIP with the electrostatic attraction of the protein by the SAM. HTHP bound to the MIP exhibits quasi-reversible DET which is reflected by a pair of well pronounced redox peaks in the cyclic voltammograms (CVs) with a formal potential of −184.4 ± 13.7 mV vs. Ag/AgCl (1 M KCl) at pH 8.0 and it was able to catalyze the cathodic reduction of peroxide. At saturation the MIP films show a 12-fold higherFor the first time a molecularly imprinted polymer (MIP) with direct electron transfer (DET) and bioelectrocatalytic activity of the target protein is presented. Thin films of MIPs for the recognition of a hexameric tyrosine-coordinated heme protein (HTHP) have been prepared by electropolymerization of scopoletin after oriented assembly of HTHP on a self-assembled monolayer (SAM) of mercaptoundecanoic acid (MUA) on gold electrodes. Cavities which should resemble the shape and size of HTHP were formed by template removal. Rebinding of the target protein sums up the recognition by non-covalent interactions between the protein and the MIP with the electrostatic attraction of the protein by the SAM. HTHP bound to the MIP exhibits quasi-reversible DET which is reflected by a pair of well pronounced redox peaks in the cyclic voltammograms (CVs) with a formal potential of −184.4 ± 13.7 mV vs. Ag/AgCl (1 M KCl) at pH 8.0 and it was able to catalyze the cathodic reduction of peroxide. At saturation the MIP films show a 12-fold higher electroactive surface concentration of HTHP than the non-imprinted polymer (NIP).zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Lei Peng, Aysu YarmanORCiDGND, Katharina J. JetzschmannORCiD, Jae-Hun Jeoung, Daniel SchadORCiDGND, Holger Dobbek, Ursula WollenbergerORCiDGND, Frieder W. SchellerORCiDGND
URN:urn:nbn:de:kobv:517-opus4-400627
Schriftenreihe (Bandnummer):Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe (362)
Publikationstyp:Postprint
Sprache:Englisch
Datum der Erstveröffentlichung:22.09.2017
Erscheinungsjahr:2017
Veröffentlichende Institution:Universität Potsdam
Datum der Freischaltung:22.09.2017
Freies Schlagwort / Tag:bioelectrocatalysis; direct electron transfer; hydrogen peroxide; molecularly imprinted polymers; self-assembled monolayer
Seitenanzahl:11
Quelle:Sensors 16 (2016) Nr. 3. - DOI: 10.3390/s16030272
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:6 Technik, Medizin, angewandte Wissenschaften / 62 Ingenieurwissenschaften / 620 Ingenieurwissenschaften und zugeordnete Tätigkeiten
Peer Review:Referiert
Publikationsweg:Open Access
Fördermittelquelle:Multidisciplinary Digital Publishing Institute (MDPI)
Lizenz (Deutsch):License LogoCC-BY - Namensnennung 4.0 International
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