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Enzyme self-assembly on naked iron oxide nanoparticles for aminoaldehyde biosensing
M. Magro, D. Baratella, G. Miotto, J. Frömmel, M. Šebela, M. Kopečná, E. Agostinelli, F. Vianello,
Jazyk angličtina Země Rakousko
Typ dokumentu časopisecké články
Grantová podpora
60A06-7411
MIUR
60A06-8055
MIUR
CPDA159850
Università degli Studi di Padova
LO1204
Ministerstvo Školství, Mládeže a Tělovýchovy
NLK
ProQuest Central
od 1997-03-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2010-01-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-03-01 do Před 1 rokem
Springer Nature OA/Free Journals
od 1991-02-01
- MeSH
- aldehyddehydrogenasa metabolismus MeSH
- aldehydy analýza MeSH
- biosenzitivní techniky * MeSH
- elektrochemické techniky MeSH
- enzymy imobilizované metabolismus MeSH
- kovové nanočástice chemie MeSH
- propylaminy analýza MeSH
- Solanum lycopersicum enzymologie MeSH
- železité sloučeniny chemie MeSH
- Publikační typ
- časopisecké články MeSH
The preservation of enzymatic activity is a fundamental requirement for exploiting hybrid nano-bio-conjugates, and the control over protein-nanoparticle interactions, leading to stable and catalytically active hybrids, represents the key for designing new biosensing platforms. In this scenario, surface active maghemite nanoparticles (SAMNs) represent a new class of naked magnetic nanoparticles, displaying peculiar electrocatalytic features and the ability to selectively bind proteins. Recombinant aminoaldehyde dehydrogenase from tomato (SlAMADH1) was used as a model protein, and successfully immobilized by self-assembly on the surface of naked SAMNs, where its enzymatic activity resulted preserved for more than 6 months. The hybrid nanomaterial (SAMN@SlAMADH1) was characterized by UV-Vis spectroscopy, mass spectrometry, and TEM microscopy, and applied for the development of a biosensor for the determination of aminoaldehydes in alcoholic beverages. Measurements were carried out in a low volume electrochemical flow cell comprising a SAMN modified carbon paste electrode for the coulometric determination of the NADH produced during the enzymatic catalysis. The present findings, besides representing the first example of an electrochemical biosensor for aminoaldehydes in an alcoholic matrix, open the door to the use of immobilized enzymes on naked metal oxides nanomaterials for biosensing.
Citace poskytuje Crossref.org
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- $a Enzyme self-assembly on naked iron oxide nanoparticles for aminoaldehyde biosensing / $c M. Magro, D. Baratella, G. Miotto, J. Frömmel, M. Šebela, M. Kopečná, E. Agostinelli, F. Vianello,
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- $a The preservation of enzymatic activity is a fundamental requirement for exploiting hybrid nano-bio-conjugates, and the control over protein-nanoparticle interactions, leading to stable and catalytically active hybrids, represents the key for designing new biosensing platforms. In this scenario, surface active maghemite nanoparticles (SAMNs) represent a new class of naked magnetic nanoparticles, displaying peculiar electrocatalytic features and the ability to selectively bind proteins. Recombinant aminoaldehyde dehydrogenase from tomato (SlAMADH1) was used as a model protein, and successfully immobilized by self-assembly on the surface of naked SAMNs, where its enzymatic activity resulted preserved for more than 6 months. The hybrid nanomaterial (SAMN@SlAMADH1) was characterized by UV-Vis spectroscopy, mass spectrometry, and TEM microscopy, and applied for the development of a biosensor for the determination of aminoaldehydes in alcoholic beverages. Measurements were carried out in a low volume electrochemical flow cell comprising a SAMN modified carbon paste electrode for the coulometric determination of the NADH produced during the enzymatic catalysis. The present findings, besides representing the first example of an electrochemical biosensor for aminoaldehydes in an alcoholic matrix, open the door to the use of immobilized enzymes on naked metal oxides nanomaterials for biosensing.
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- $a Frömmel, Jan $u Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University in Olomouc, Šlechtitelu 11, 78371, Olomouc, Czech Republic.
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