Redox-active concanavalin a: Synthesis, characterization, and recognition-driven assembly of interfacial architectures for bioelectronic applications

The convergence of chemistry, biology, and materials science has paved the way to the emergence of hybrid nanobuilding blocks that incorporate the highly selective recognition properties of biomolecules, with the tailorable functional capabilities of inorganic molecules. In this work, we describe fo...

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Autor principal: Pallarola, D.
Otros Autores: Queralto, N., Knoll, W., Ceoli, Azzaroni, O., Battaglini, Fernando
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2010
Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a concanavalin A, 11028-71-0; Concanavalin A, 11028-71-0 
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100 1 |a Pallarola, D. 
245 1 0 |a Redox-active concanavalin a: Synthesis, characterization, and recognition-driven assembly of interfacial architectures for bioelectronic applications 
260 |c 2010 
270 1 0 |m Azzaroni, O.; Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Departamento de Química, Universidad Nacional de la Plata, CC 16 Suc. 4, (1900) La Plata, Argentina; email: azzaroni@inifta.unlp.edu.ar 
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506 |2 openaire  |e Política editorial 
520 3 |a The convergence of chemistry, biology, and materials science has paved the way to the emergence of hybrid nanobuilding blocks that incorporate the highly selective recognition properties of biomolecules, with the tailorable functional capabilities of inorganic molecules. In this work, we describe for the first time the decoration of concanavalin A (Con A), a protein with the ability to recognize sugars and form glycoconjugates, with Os(II) redox-active complexes. This strategy enabled the construction of electroactive biosupramolecular materials whose redox potentials could be easily modulated through the facile molecular modification of the electroactive inorganic complexes. Small-angle X-ray scattering (SAXS), steady-state fluorescence, surface plasmon resonance (SPR) spectroscopy, matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF-MS), and differential-pulsed (DPV) and cyclic voltammetry (CV) were used to characterize the structural and functional features of the synthesized biohybrid building blocks as well as their respective supramolecular assemblies built up on gold electrodes. By harnessing the electroactive and carbohydrate-recognition properties of these tailor-made biohybrid building blocks, we were able to integrate glucose oxidase (GOx) onto gold electrodes via sugar'lectin interactions. The redox activity of the Os-modified Con A interlayer allowed the electronic connection between the multilayered GOx assemblies and the metal electrode as evidenced by the well-defined bioelectrocatalytic response exhibited by the biomolecular assemblies in the presence of the glucose in solution. We consider that this approach based on the spontaneous formation of redox-active biosupramolecular assemblies driven by recognition processes can be of practical relevance for the facile design of biosensors, as well as for the construction of new multifunctional bioelectrochemical systems. © 2010 American Chemical Society.  |l eng 
593 |a Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas (INIFTA), Departamento de Química, Universidad Nacional de la Plata, CC 16 Suc. 4, (1900) La Plata, Argentina 
593 |a Max-Planck-Institut für Polymerforschung, Ackermannweg 10, (55128) Mainz, Germany 
593 |a Austrian Institute of Technology (AIT), Donau-City-Strasse 1, (1220) Vienna, Austria 
593 |a INQUIMAE, Departamento de Química InorgÁnica, Ciudad Universitaria, Pabellón 2, C1428EHA Buenos Aires, Argentina 
690 1 0 |a BIO-MOLECULAR 
690 1 0 |a BIOELECTROCHEMICAL SYSTEMS 
690 1 0 |a BIOELECTRONIC APPLICATIONS 
690 1 0 |a BUILDING BLOCKES 
690 1 0 |a CONCANAVALIN A 
690 1 0 |a ELECTROACTIVE 
690 1 0 |a FUNCTIONAL CAPABILITIES 
690 1 0 |a FUNCTIONAL FEATURES 
690 1 0 |a GLYCOCONJUGATES 
690 1 0 |a GOLD ELECTRODES 
690 1 0 |a INORGANIC COMPLEXES 
690 1 0 |a INORGANIC MOLECULES 
690 1 0 |a INTERFACIAL ARCHITECTURE 
690 1 0 |a MALDI TOF MS 
690 1 0 |a MATRIX-ASSISTED LASER DESORPTION/IONIZATION-TIME-OF-FLIGHT MASS SPECTROMETRY 
690 1 0 |a METAL ELECTRODES 
690 1 0 |a MOLECULAR MODIFICATION 
690 1 0 |a MULTI-LAYERED 
690 1 0 |a NANOBUILDING BLOCKS 
690 1 0 |a RECOGNITION PROCESS 
690 1 0 |a RECOGNITION PROPERTIES 
690 1 0 |a REDOX ACTIVITY 
690 1 0 |a REDOX POTENTIALS 
690 1 0 |a REDOX-ACTIVE 
690 1 0 |a SELECTIVE RECOGNITION 
690 1 0 |a SMALL ANGLE X-RAY SCATTERING 
690 1 0 |a SPONTANEOUS FORMATION 
690 1 0 |a STEADY-STATE FLUORESCENCE 
690 1 0 |a SUPRAMOLECULAR ASSEMBLIES 
690 1 0 |a SURFACE PLASMON RESONANCE SPECTROSCOPY 
690 1 0 |a BIOSENSORS 
690 1 0 |a CARBOHYDRATES 
690 1 0 |a CHARACTERIZATION 
690 1 0 |a COMPLEXATION 
690 1 0 |a CYCLIC VOLTAMMETRY 
690 1 0 |a DESORPTION 
690 1 0 |a ELECTRODES 
690 1 0 |a FUNCTIONAL POLYMERS 
690 1 0 |a GLUCOSE 
690 1 0 |a GLUCOSE OXIDASE 
690 1 0 |a GLUCOSE SENSORS 
690 1 0 |a HYBRID MATERIALS 
690 1 0 |a MASS SPECTROMETRY 
690 1 0 |a MOLECULAR BIOLOGY 
690 1 0 |a OSMIUM 
690 1 0 |a PULSED LASER APPLICATIONS 
690 1 0 |a PULSED LASERS 
690 1 0 |a REDOX REACTIONS 
690 1 0 |a SUGAR (SUCROSE) 
690 1 0 |a SURFACE PLASMON RESONANCE 
690 1 0 |a X RAY SCATTERING 
690 1 0 |a BUILDING MATERIALS 
690 1 0 |a CONCANAVALIN A 
690 1 0 |a NANOMATERIAL 
690 1 0 |a ARTICLE 
690 1 0 |a CHEMISTRY 
690 1 0 |a ELECTROCHEMISTRY 
690 1 0 |a MASS SPECTROMETRY 
690 1 0 |a SMALL ANGLE SCATTERING 
690 1 0 |a SURFACE PLASMON RESONANCE 
690 1 0 |a THEORETICAL MODEL 
690 1 0 |a CONCANAVALIN A 
690 1 0 |a ELECTROCHEMISTRY 
690 1 0 |a MODELS, THEORETICAL 
690 1 0 |a NANOSTRUCTURES 
690 1 0 |a SCATTERING, SMALL ANGLE 
690 1 0 |a SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION 
690 1 0 |a SURFACE PLASMON RESONANCE 
700 1 |a Queralto, N. 
700 1 |a Knoll, W. 
700 1 |a Ceoli 
700 1 |a Azzaroni, O. 
700 1 |a Battaglini, Fernando 
773 0 |d 2010  |g v. 26  |h pp. 13684-13696  |k n. 16  |p Langmuir  |x 07437463  |t Langmuir 
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856 4 0 |u https://doi.org/10.1021/la100486g  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_07437463_v26_n16_p13684_Pallarola  |y Handle 
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