Enzyme solid-state support assays: a surface plasmon resonance and mass spectrometry coupled study of immobilized insulin degrading enzyme(862 views) Grasso G, Bush AI, D'Agata R, Rizzarelli E, Spoto G
Keywords: Conformational Change, Insulin Degrading Enzyme, Mass Spectrometry, Solid-State Assay, Surface Plasmon Resonance, Animals, Atmospheric Pressure, Cattle, Immobilized, Gold, Insulysin, Kinetics, Microfluidics, Protein Binding, Protein Conformation, Matrix-Assisted Laser Desorption-Ionization, Spodoptera,
Affiliations: *** IBB - CNR ***
Dipartimento Scienze Chimiche, Universita di Catania, v.le A. Doria 6, 95125, Catania, Italy. grassog@unict.it
Department of Psychiatry, Massachusetts General Hospital, Charlestone, MA, United States
Department of Pathology, Mental Health Research Institute of Victoria, University of Melbourne, Parkville, Australia
Istituto di Biostrutture e Bioimmagini, CNR, v.le A. Doria 6, 95125 Catania, Italy
References: Not available.
Enzyme solid-state support assays: a surface plasmon resonance and mass spectrometry coupled study of immobilized insulin degrading enzyme
Solid-support based assays offer several advantages that are not normally available in solution. Enzymes that are anchored on gold surfaces can interact with several different molecules, opening the way to high throughput array format based assays. In this scenario, surface plasmon resonance (SPR) and mass spectrometry (MS) investigations have often been applied to analyze the interaction between immobilized enzyme and its substrate molecules in a tag-free environment. Here, we propose a SPR-MS combined experimental approach aimed at studying insulin degrading enzyme (IDE) immobilized onto gold surfaces and its ability to interact with insulin. The latter is delivered by a microfluidic system to the IDE functionalized surface and the activity of the immobilized enzyme is verified by atmospheric pressure/matrix assisted laser desorption ionization (AP/MALDI) MS analysis. The SPR experiments allow the calculation of the kinetic constants involved for the interaction between immobilized IDE and insulin molecules and evidence of IDE conformational change upon insulin binding is also obtained.
Enzyme solid-state support assays: a surface plasmon resonance and mass spectrometry coupled study of immobilized insulin degrading enzyme