Advancing Techniques for Investigating the Enzyme-Electrode Interface.


Journal

Accounts of chemical research
ISSN: 1520-4898
Titre abrégé: Acc Chem Res
Pays: United States
ID NLM: 0157313

Informations de publication

Date de publication:
21 05 2019
Historique:
pubmed: 3 5 2019
medline: 9 7 2020
entrez: 3 5 2019
Statut: ppublish

Résumé

Enzymes are the essential catalytic components of biology and adsorbing redox-active enzymes on electrode surfaces enables the direct probing of their function. Through standard electrochemical measurements, catalytic activity, reversibility and stability, potentials of redox-active cofactors, and interfacial electron transfer rates can be readily measured. Mechanistic investigations on the high electrocatalytic rates and selectivity of enzymes may yield inspiration for the design of synthetic molecular and heterogeneous electrocatalysts. Electrochemical investigations of enzymes also aid in our understanding of their activity within their biological environment and why they evolved in their present structure and function. However, the conventional array of electrochemical techniques (e.g., voltammetry and chronoamperometry) alone offers a limited picture of the enzyme-electrode interface. How many enzymes are loaded onto an electrode? In which orientation(s) are they bound? What fraction is active, and are single or multilayers formed? Does this static picture change over time, applied voltage, or chemical environment? How does charge transfer through various intraprotein cofactors contribute to the overall performance and catalytic bias? What is the distribution of individual enzyme activities within an ensemble of active protein films? These are central questions for the understanding of the enzyme-electrode interface, and a multidisciplinary approach is required to deliver insightful answers. Complementing standard electrochemical experiments with an orthogonal set of techniques has recently allowed to provide a more complete picture of enzyme-electrode systems. Within this framework, we first discuss a brief history of achievements and challenges in enzyme electrochemistry. We subsequently describe how the aforementioned challenges can be overcome by applying advanced electrochemical techniques, quartz-crystal microbalance measurements, and spectroscopic, namely, resonance Raman and infrared, analysis. For example, rotating ring disk electrochemistry permits the simultaneous determination of reaction kinetics and quantification of generated products. In addition, recording changes in frequency and dissipation in a quartz crystal microbalance allows to shed light into enzyme loading, relative orientation, clustering, and denaturation at the electrode surface. Resonance Raman spectroscopy yields information on ligation and redox state of enzyme cofactors, whereas infrared spectroscopy provides insights into active site states and the protein secondary and tertiary structure. The development of these emerging methods for the analysis of the enzyme-electrode interface is the primary focus of this Account. We also take a critical look at the remaining gaps in our understanding and challenges lying ahead toward attaining a complete mechanistic picture of the enzyme-electrode interface.

Identifiants

pubmed: 31042353
doi: 10.1021/acs.accounts.9b00087
pmc: PMC6533600
doi:

Substances chimiques

Coenzymes 0
Enzymes, Immobilized 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1439-1448

Références

J Am Chem Soc. 2002 Dec 11;124(49):14724-35
pubmed: 12465985
Q Rev Biophys. 2002 Nov;35(4):369-430
pubmed: 12621861
Biochemistry. 2004 Feb 17;43(6):1667-74
pubmed: 14769044
Chem Rev. 2007 Oct;107(10):4366-413
pubmed: 17845060
J Biol Inorg Chem. 2008 Jan;13(1):85-96
pubmed: 17899220
J Am Chem Soc. 2008 Jul 30;130(30):9844-8
pubmed: 18593159
Chem Rev. 2008 Jul;108(7):2379-438
pubmed: 18620368
Biosens Bioelectron. 2009 Apr 15;24(8):2313-22
pubmed: 19022645
ACS Nano. 2009 Dec 22;3(12):4055-61
pubmed: 19947646
J Am Chem Soc. 2010 Apr 7;132(13):4848-57
pubmed: 20230028
Chem Commun (Camb). 2011 Feb 14;47(6):1863-5
pubmed: 21127815
Faraday Discuss. 2011;148:345-57; discussion 421-41
pubmed: 21322492
FEBS J. 2011 May;278(9):1382-90
pubmed: 21352495
Angew Chem Int Ed Engl. 2011 Mar 7;50(11):2632-4
pubmed: 21370354
J Phys Chem B. 2011 Sep 1;115(34):10368-74
pubmed: 21761881
Proc Natl Acad Sci U S A. 2011 Aug 23;108(34):14049-54
pubmed: 21844379
J Am Chem Soc. 2012 Jan 25;134(3):1577-82
pubmed: 21916466
Angew Chem Int Ed Engl. 2012 Jan 23;51(4):953-6
pubmed: 22173906
J Am Chem Soc. 2013 Mar 13;135(10):3926-38
pubmed: 23362993
Phys Chem Chem Phys. 2013 May 21;15(19):7055-9
pubmed: 23552374
J Am Chem Soc. 2013 Jul 24;135(29):10610-3
pubmed: 23829513
Biochim Biophys Acta. 2013 Dec;1834(12):2849-58
pubmed: 23928299
Phys Chem Chem Phys. 2014 Jun 28;16(24):11822-33
pubmed: 24556983
Electrochim Acta. 2013 Nov 1;110:79-85
pubmed: 24634538
Chem Soc Rev. 2014 Sep 21;43(18):6485-97
pubmed: 24668258
J Am Chem Soc. 2014 Jul 16;136(28):9870-3
pubmed: 24956459
Nat Chem. 2014 Sep;6(9):822-7
pubmed: 25143219
Chem Commun (Camb). 2015 Feb 21;51(15):3255-7
pubmed: 25608720
J Am Chem Soc. 2015 Jul 8;137(26):8541-9
pubmed: 26046591
PLoS One. 2015 Jun 19;10(6):e0129940
pubmed: 26091174
J Phys Chem B. 2015 Jul 30;119(30):9586-91
pubmed: 26135359
PLoS One. 2015 Nov 18;10(11):e0143101
pubmed: 26580976
Chem Commun (Camb). 2016 May 31;52(46):7390-3
pubmed: 27193068
Small. 2016 Sep;12(34):4649-61
pubmed: 27377976
Acc Chem Res. 2016 Oct 18;49(10):2328-2335
pubmed: 27626289
J Am Chem Soc. 2017 Mar 8;139(9):3324-3327
pubmed: 28221032
Proc Natl Acad Sci U S A. 2017 Apr 11;114(15):3843-3848
pubmed: 28348243
J Am Chem Soc. 2017 Jul 26;139(29):9927-9936
pubmed: 28635274
J Am Chem Soc. 2017 Aug 9;139(31):10677-10686
pubmed: 28697596
Org Biomol Chem. 2017 Nov 22;15(45):9539-9551
pubmed: 28932860
Chem Sci. 2017 Sep 1;8(9):6423-6432
pubmed: 29163928
Angew Chem Int Ed Engl. 2018 Jun 11;57(24):7225-7229
pubmed: 29573138
Angew Chem Int Ed Engl. 2018 Aug 13;57(33):10595-10599
pubmed: 29888857
Chem Sci. 2018 May 8;9(24):5322-5333
pubmed: 30009004
J Phys Chem Lett. 2018 Sep 6;9(17):5196-5200
pubmed: 30141632
J Am Chem Soc. 2018 Dec 26;140(51):17923-17931
pubmed: 30188698
Nat Nanotechnol. 2018 Oct;13(10):890-899
pubmed: 30291349
Nano Lett. 2019 Mar 13;19(3):1844-1850
pubmed: 30689393
Angew Chem Int Ed Engl. 2019 Mar 26;58(14):4601-4605
pubmed: 30724432
Anal Chim Acta. 1973 May;64(3):439-55
pubmed: 4701057
Anal Chem. 1976 Oct;48(12):1679-86
pubmed: 970629

Auteurs

Nikolay Kornienko (N)

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.
Department of Chemistry , Université de Montréal , Roger-Gaudry Building , Montreal , Quebec H3C 3J7 , Canada.

Khoa H Ly (KH)

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.
Fakultät für Chemie und Lebensmittelchemie , Technische Universität Dresden , 01062 Dresden , Germany.

William E Robinson (WE)

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.
Institute for Molecules and Materials , Radboud University , Heyendaalseweg 135 , 6525 AJ Nijmegen , The Netherlands.

Nina Heidary (N)

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.
Department of Chemistry , Université de Montréal , Roger-Gaudry Building , Montreal , Quebec H3C 3J7 , Canada.

Jenny Z Zhang (JZ)

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.

Erwin Reisner (E)

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , U.K.

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Classifications MeSH