Affinity-based biosensors employing surface-bound biomolecules for analyte detection are important tools in clinical diagnostics and drug development. In this context, electrolyte-gated organic transistors (EGOTs) are emerging as ultrasensitive label-free biosensors. In this study, we present an EGOT sensor integrated within a microfluidic system. The sensor utilizes the cytomegalovirus (CMV) phosphoprotein 65 as a biorecognition element to detect the pathological biomarker human anti-cytomegalovirus antibody in solution. The biorecognition element is grafted onto the gate electrode by exploiting the polyhistidine-tag technology. Real-time monitoring of the EGOT response, coupled with a twocompartment kinetic model analysis, enables the determination of analyte concentration, binding kinetics, and thermodynamics of the interaction. The analysis of the relevant kinetic parameters of the binding process yields a reliable value for the thermodynamic equilibrium constant and suggests that the measured deviations from the Langmuir binding model arise from the co-existence of binding sites with different affinities toward the antibodies.
Dynamic studies of antibody-antigen interactions with an electrolyte-gated organic transistor / Manco Urbina, P. A.; Paradisi, A.; Hasler, R.; Sensi, M.; Berto, M.; Saygin, G. D.; Dostalek, J.; Pinti, M.; Greco, P.; Borsari, M.; Knoll, W.; Bortolotti, C. A.; Biscarini, F.. - In: CELL REPORTS PHYSICAL SCIENCE. - ISSN 2666-3864. - 5:8(2024), pp. N/A-N/A. [10.1016/j.xcrp.2024.101919]
Dynamic studies of antibody-antigen interactions with an electrolyte-gated organic transistor
Manco Urbina P. A.;Paradisi A.
;Sensi M.;Berto M.;Saygin G. D.;Pinti M.;Borsari M.;Bortolotti C. A.
;Biscarini F.
2024
Abstract
Affinity-based biosensors employing surface-bound biomolecules for analyte detection are important tools in clinical diagnostics and drug development. In this context, electrolyte-gated organic transistors (EGOTs) are emerging as ultrasensitive label-free biosensors. In this study, we present an EGOT sensor integrated within a microfluidic system. The sensor utilizes the cytomegalovirus (CMV) phosphoprotein 65 as a biorecognition element to detect the pathological biomarker human anti-cytomegalovirus antibody in solution. The biorecognition element is grafted onto the gate electrode by exploiting the polyhistidine-tag technology. Real-time monitoring of the EGOT response, coupled with a twocompartment kinetic model analysis, enables the determination of analyte concentration, binding kinetics, and thermodynamics of the interaction. The analysis of the relevant kinetic parameters of the binding process yields a reliable value for the thermodynamic equilibrium constant and suggests that the measured deviations from the Langmuir binding model arise from the co-existence of binding sites with different affinities toward the antibodies.File | Dimensione | Formato | |
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Descrizione: Pubblicata in OA gold sulla rivista Cell Reports Physical Science all'indirizzo: http://www.cell.com/article/S2666386424001668/
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