Abstract

Interaction between nanostructured semiconductor thin layers and immune complex based proteins is a fundamental issue of the formation of nanobiointerface in the various biosensors, in particular, optical biosensors. In this work, the main aspects of the interaction between photoluminescent TiO2 nanoparticles and Bovine leucosis virus (BLV) protein gp51, used as a model protein, during the formation of photoluminescence based immunosensor have been discussed. The antigens of gp51 were immobilized on the surface of a nanostructured TiO2 thin film formed on the glass substrates. As a result, an increase of the photoluminescence (PL) signal intensity and PL peak shift from 517 nm to 499 nm were observed. An incubation of TiO2/gp51 structure in a solution containing anti-gp51 antibodies resulted in the backward PL peak shift from 499 nm to 516 nm and decrease of the PL intensity. The main reason of the changes in the PL spectra (i.e. PL maxima shifts and PL intensity variations) as a result of BLV protein gp51 adsorption on the surface TiO2 thin film is an electrostatic interaction between negatively charged surface of TiO2 and positively charged atoms and groups provided by the adsorbed gp51 protein due to the presence of partial uncompensated charges within the proteins.

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