Controlling Redox Enzyme Orientation at Planar Electrodes
Redox enzymes, which catalyze reactions involving electron transfers in living organisms, are very promising components of biotechnological devices, and can be envisioned for sensing applications as well as for energy conversion. In this context, one of the most significant challenges is to achieve...
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doaj-85bcb9fa49574ef1b4c67a30b46b21062020-11-24T22:18:17ZengMDPI AGCatalysts2073-43442018-05-018519210.3390/catal8050192catal8050192Controlling Redox Enzyme Orientation at Planar ElectrodesVivek Pratap Hitaishi0Romain Clement1Nicolas Bourassin2Marc Baaden3Anne de Poulpiquet4Sophie Sacquin-Mora5Alexandre Ciaccafava6Elisabeth Lojou7National Center for Scientific Research (CNRS), Aix Marseille University, BIP, UMR 7281, 31 Chemin Aiguier, 13009 Marseille, FranceNational Center for Scientific Research (CNRS), Aix Marseille University, BIP, UMR 7281, 31 Chemin Aiguier, 13009 Marseille, FranceLaboratoire de Biochimie Théorique, National Center for Scientific Research (CNRS), UPR9080, Université Paris Diderot, Sorbonne Paris Cité, PSL Research University, 13 rue Pierre et Marie Curie, 75005 Paris, FranceLaboratoire de Biochimie Théorique, National Center for Scientific Research (CNRS), UPR9080, Université Paris Diderot, Sorbonne Paris Cité, PSL Research University, 13 rue Pierre et Marie Curie, 75005 Paris, FranceNational Center for Scientific Research (CNRS), Aix Marseille University, BIP, UMR 7281, 31 Chemin Aiguier, 13009 Marseille, FranceLaboratoire de Biochimie Théorique, National Center for Scientific Research (CNRS), UPR9080, Université Paris Diderot, Sorbonne Paris Cité, PSL Research University, 13 rue Pierre et Marie Curie, 75005 Paris, FranceChemistry and Biology of Membranes and Nanoobjects, UMR 5248 CNRS, University of Bordeaux, Bat. B14 allée Geoffroy St. Hilaire, 33600 Pessac, FranceNational Center for Scientific Research (CNRS), Aix Marseille University, BIP, UMR 7281, 31 Chemin Aiguier, 13009 Marseille, FranceRedox enzymes, which catalyze reactions involving electron transfers in living organisms, are very promising components of biotechnological devices, and can be envisioned for sensing applications as well as for energy conversion. In this context, one of the most significant challenges is to achieve efficient direct electron transfer by tunneling between enzymes and conductive surfaces. Based on various examples of bioelectrochemical studies described in the recent literature, this review discusses the issue of enzyme immobilization at planar electrode interfaces. The fundamental importance of controlling enzyme orientation, how to obtain such orientation, and how it can be verified experimentally or by modeling are the three main directions explored. Since redox enzymes are sizable proteins with anisotropic properties, achieving their functional immobilization requires a specific and controlled orientation on the electrode surface. All the factors influenced by this orientation are described, ranging from electronic conductivity to efficiency of substrate supply. The specificities of the enzymatic molecule, surface properties, and dipole moment, which in turn influence the orientation, are introduced. Various ways of ensuring functional immobilization through tuning of both the enzyme and the electrode surface are then described. Finally, the review deals with analytical techniques that have enabled characterization and quantification of successful achievement of the desired orientation. The rich contributions of electrochemistry, spectroscopy (especially infrared spectroscopy), modeling, and microscopy are featured, along with their limitations.http://www.mdpi.com/2073-4344/8/5/192metalloenzymesenzyme immobilizationenzyme orientationelectrodesbioelectrocatalysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vivek Pratap Hitaishi Romain Clement Nicolas Bourassin Marc Baaden Anne de Poulpiquet Sophie Sacquin-Mora Alexandre Ciaccafava Elisabeth Lojou |
spellingShingle |
Vivek Pratap Hitaishi Romain Clement Nicolas Bourassin Marc Baaden Anne de Poulpiquet Sophie Sacquin-Mora Alexandre Ciaccafava Elisabeth Lojou Controlling Redox Enzyme Orientation at Planar Electrodes Catalysts metalloenzymes enzyme immobilization enzyme orientation electrodes bioelectrocatalysis |
author_facet |
Vivek Pratap Hitaishi Romain Clement Nicolas Bourassin Marc Baaden Anne de Poulpiquet Sophie Sacquin-Mora Alexandre Ciaccafava Elisabeth Lojou |
author_sort |
Vivek Pratap Hitaishi |
title |
Controlling Redox Enzyme Orientation at Planar Electrodes |
title_short |
Controlling Redox Enzyme Orientation at Planar Electrodes |
title_full |
Controlling Redox Enzyme Orientation at Planar Electrodes |
title_fullStr |
Controlling Redox Enzyme Orientation at Planar Electrodes |
title_full_unstemmed |
Controlling Redox Enzyme Orientation at Planar Electrodes |
title_sort |
controlling redox enzyme orientation at planar electrodes |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2018-05-01 |
description |
Redox enzymes, which catalyze reactions involving electron transfers in living organisms, are very promising components of biotechnological devices, and can be envisioned for sensing applications as well as for energy conversion. In this context, one of the most significant challenges is to achieve efficient direct electron transfer by tunneling between enzymes and conductive surfaces. Based on various examples of bioelectrochemical studies described in the recent literature, this review discusses the issue of enzyme immobilization at planar electrode interfaces. The fundamental importance of controlling enzyme orientation, how to obtain such orientation, and how it can be verified experimentally or by modeling are the three main directions explored. Since redox enzymes are sizable proteins with anisotropic properties, achieving their functional immobilization requires a specific and controlled orientation on the electrode surface. All the factors influenced by this orientation are described, ranging from electronic conductivity to efficiency of substrate supply. The specificities of the enzymatic molecule, surface properties, and dipole moment, which in turn influence the orientation, are introduced. Various ways of ensuring functional immobilization through tuning of both the enzyme and the electrode surface are then described. Finally, the review deals with analytical techniques that have enabled characterization and quantification of successful achievement of the desired orientation. The rich contributions of electrochemistry, spectroscopy (especially infrared spectroscopy), modeling, and microscopy are featured, along with their limitations. |
topic |
metalloenzymes enzyme immobilization enzyme orientation electrodes bioelectrocatalysis |
url |
http://www.mdpi.com/2073-4344/8/5/192 |
work_keys_str_mv |
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