Gastric ATPase phosphorylation/dephosphorylation monitored by new FTIR-based BIA–ATR biosensors
Author(s) -
A. Goldsztein,
S. Babar,
M. Voué,
J. De Coninck,
J. Conti,
Jacqueline MarchandBrynaert,
Sabrina Devouge,
Fabrice Homblé,
Erik Goormaghtigh
Publication year - 2010
Publication title -
spectroscopy an international journal
Language(s) - English
Resource type - Journals
eISSN - 1875-922X
pISSN - 0712-4813
DOI - 10.1155/2010/793594
Subject(s) - attenuated total reflection , dephosphorylation , biosensor , fourier transform infrared spectroscopy , chemistry , membrane , ligand (biochemistry) , phosphorylation , infrared spectroscopy , biophysics , biochemistry , receptor , phosphatase , organic chemistry , chemical engineering , biology , engineering
Biosensors are composite devices suitable for the investigation of receptor–ligand interactions. In this paper we present the specific application to a membrane embedded protein of a new sensor device, so-called BIA–ATR, based on Attenuated Total Reflection–Fourier Transform Infrared (ATR–FTIR) spectroscopy. It consists in a functionalised ATR germanium crystal whose surface has been covalently modified to adsorb a biomembrane. Detection of the ligand–receptor interaction is achieved using FTIR spectroscopy. We report the specific detection of the phosphorylation/dephosphorylation of the H + /K + gastric ATPase. The H + , K + -ATPase is a particularly large protein entity. This glycosylated protein contains more than 1300 residues and is embedded in a lipid membrane. Yet we demonstrate that the BIA–ATR sensor is capable of monitoring the binding of a single phosphate on such a large protein entity. Furthermore, we also demonstrate the potential of the approach to monitor the kinetics of binding and dissociation of the ligand.
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