Protein conformational changes revealed by optical spectroscopic reflectometry in porous silicon multilayers

J Phys Condens Matter. 2009 Jan 21;21(3):035115. doi: 10.1088/0953-8984/21/3/035115. Epub 2008 Dec 15.

Abstract

The protein-ligand molecular interactions imply strong geometrical and structural rearrangements of the biological complex which are normally detected by high sensitivity optical techniques such as time-resolved fluorescence microscopy. In this work, we have measured, by optical spectroscopic reflectometry in the visible-near-infrared region, the interaction between a sugar binding protein (SBP), covalently bound on the surface of a porous silicon (PSi) microcavity, and glucose, at different concentrations and temperatures. Variable-angle spectroscopic ellipsometric (VASE) characterization of protein-functionalized PSi layers confirms that the protein-ligand system has an overall volume smaller than the SBP alone.