首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Contact Free Impedance Methodology for Investigating Enzymatic Reactions into Dielectric Polymer Microchip
Authors:Mathilde Faure  Mohammed Kechadi  Bruno Sotta  Jean Gamby  Bernard Tribollet
Institution:1. Laboratoire Interfaces et Systèmes Electrochimiques UPR 15 CNRS;2. 4 Place Jussieu, case postale 133, F‐75252 Paris, France;3. UPMC Sorbonne Universités, 4 Place Jussieu, case postale 133, F‐75252 Paris, France;4. UPMC, UR 5, Laboratoire de Physiologie cellulaire et Moléculaire des Plantes, 4 Place Jussieu, F‐75005 Paris, France
Abstract:A methodology for free contact microchannel impedance measurements through a dielectric microchip was developed for monitoring the kinetics of enzymatic reactions. For that purpose, we propose a procedure which consists of subtracting the impedance contribution of the dielectric polymer layer, which separates the two parallel microband electrodes embedded in it, from the global microchip impedance. This operation allows microchannel impedance enhancement for real time monitoring of impedance modulus changes without direct electrical contact. Application for determination of kinetic parameters of enzyme‐substrate reaction independently of optical or electrochemical properties of the substrates is demonstrated. Hydrolysis 4‐nitrophenylphosphate (pNPP) and 4‐aminophenylphosphate (pAPP), which are two substrates for Alkaline Phosphatase (ALP), are taken as examples. Moreover, signal amplification response of the impedance modulus is achieved by the use of superparamagnetic microbeads as enzyme supports. Plotting the maximum rate against the ALP concentration gives rise to straight lines with a slope that is the hydrolysis catalytic pseudo first‐order rate constant, kcat. Sensitivity, selectivity and reproducibility of these measurements have been demonstrated comparatively with both substrates. kcat values were 103 s?1 and 52 s?1 with pAPP and pNPP, respectively.
Keywords:Impedance  Dielectrics  Polymer  Microchannel  Enzyme  Microbeads
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号