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dc.contributor.authorOkhokhonin, A. V.en
dc.contributor.authorDomanskyi, S.en
dc.contributor.authorFilipov, Y.en
dc.contributor.authorGamella, M.en
dc.contributor.authorKozitsina, A. N.en
dc.contributor.authorPrivman, V.en
dc.contributor.authorKatz, E.en
dc.date.accessioned2020-09-29T09:47:04Z-
dc.date.available2020-09-29T09:47:04Z-
dc.date.issued2018-
dc.identifier.citationBiomolecular Release from Alginate-modified Electrode Triggered by Chemical Inputs Processed through a Biocatalytic Cascade – Integration of Biomolecular Computing and Actuation / A. V. Okhokhonin, S. Domanskyi, Y. Filipov, M. Gamella, et al. . — DOI 10.1002/elan.201700810 // Electroanalysis. — 2018. — Vol. 3. — Iss. 30. — P. 426-435.en
dc.identifier.issn1040-0397-
dc.identifier.otherhttps://rss.onlinelibrary.wiley.com/doi/am-pdf/10.1002/elan.201700810pdf
dc.identifier.other1good_DOI
dc.identifier.other9f4aacd9-cdf2-4625-ae83-d1187b1a1f19pure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85043592679m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/90359-
dc.description.abstractBiocatalytic cascades involving more than one or two enzyme-catalyzed step are inefficient inside alginate hydrogel prepared on an electrode surface. The problem originates from slow diffusion of intermediate products through the hydrogel from one enzyme to another. However, enzyme activity can be improved by surface immobilization. We demonstrate that a complex cascade of four consecutive biocatalytic reactions can be designed, with the enzymes immobilized in an LBL-assembled polymeric layer at the alginate-modified electrode surface. The product, hydrogen peroxide, then induces dissolution of iron-cross-linked alginate, which results in release process of entrapped biomolecular species, here fluorescently marked oligonucleotides, denoted F-DNA. The enzymatic cascade can be viewed as a biocomputing network of concatenated AND gates, activated by combinations of four chemical input signals, which trigger the release of F-DNA. The reactions, and diffusion/release processes were investigated by means of theoretical modeling. A bottleneck reaction step associated with one of the enzymes was observed. The developed system provides a model for biochemical actuation triggered by a biocomputing network of reactions. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen
dc.description.sponsorshipNational Science Foundation, NSF: CBET-1403208en
dc.description.sponsorshipRussian Science Foundation, RSF: 17-13-01096en
dc.description.sponsorshipThis work was supported by National Science Foundation, USA, (award CBET-1403208) and by Russian Science Foundation (project no. 17-13-01096).en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherWiley-VCH Verlagen
dc.relationinfo:eu-repo/grantAgreement/RSF//17-13-01096en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightspublisher-specific, author manuscript: http://onlinelibrary.wiley.com/termsAndConditions#amother
dc.sourceElectroanalysisen
dc.subjectALGINATEen
dc.subjectBIOCATALYTIC CASCADEen
dc.subjectBIOMOLECULAR COMPUTINGen
dc.subjectENZYME LOGICen
dc.subjectMODIFIED ELECTRODEen
dc.subjectSIGNAL-CONTROLLED RELEASEen
dc.titleBiomolecular Release from Alginate-modified Electrode Triggered by Chemical Inputs Processed through a Biocatalytic Cascade – Integration of Biomolecular Computing and Actuationen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/acceptedVersionen
dc.identifier.doi10.1002/elan.201700810-
dc.identifier.scopus85043592679-
local.affiliationDepartment of Chemistry and Biomolecular Science, Clarkson University, Potsdam, NY 13699, United Statesen
local.affiliationDepartment of Physics, Clarkson University, Potsdam, NY 13699, United Statesen
local.affiliationDepartment of Analytical Chemistry, Institute of Chemical Engineering, Ural Federal University, Yekaterinburg, 620002, Russian Federationen
local.contributor.employeeOkhokhonin, A.V., Department of Chemistry and Biomolecular Science, Clarkson University, Potsdam, NY 13699, United States, Department of Analytical Chemistry, Institute of Chemical Engineering, Ural Federal University, Yekaterinburg, 620002, Russian Federationru
local.contributor.employeeDomanskyi, S., Department of Physics, Clarkson University, Potsdam, NY 13699, United Statesru
local.contributor.employeeFilipov, Y., Department of Chemistry and Biomolecular Science, Clarkson University, Potsdam, NY 13699, United States, Department of Physics, Clarkson University, Potsdam, NY 13699, United Statesru
local.contributor.employeeGamella, M., Department of Chemistry and Biomolecular Science, Clarkson University, Potsdam, NY 13699, United Statesru
local.contributor.employeeKozitsina, A.N., Department of Analytical Chemistry, Institute of Chemical Engineering, Ural Federal University, Yekaterinburg, 620002, Russian Federationru
local.contributor.employeePrivman, V., Department of Physics, Clarkson University, Potsdam, NY 13699, United Statesru
local.contributor.employeeKatz, E., Department of Chemistry and Biomolecular Science, Clarkson University, Potsdam, NY 13699, United Statesru
local.description.firstpage426-
local.description.lastpage435-
local.issue30-
local.volume3-
dc.identifier.wos000427246500004-
local.identifier.pure7033540-
local.identifier.eid2-s2.0-85043592679-
local.fund.rsf17-13-01096-
local.identifier.wosWOS:000427246500004-
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