Despite
evidence showing that polymer brushes (PBs) are a powerful
tool used in biosensing for minimizing nonspecific interactions, allowing
for optimization of biosensing performance, and the fact that GaAs
semiconductors have proven to have a remarkable potential for sensitive
biomolecule detection, the combination of these two robust components
has never been considered nor evaluated as a platform for biosensing
applications. This work reports different methodologies to prepare
and tune PBs on the GaAs interface (PB–GaAs) and their potential
as useful platforms for antibody grafting, with the ultimate goal
of demonstrating the innovative and attractive character of the PB–GaAs
interfaces in the enhanced capture of antibodies and control of nonspecific
interactions. Three different functionalization approaches were explored,
one “grafting-to” and two “grafting-from,”
in which atom transfer radical polymerization (ATRP) was performed,
followed by their corresponding characterizations. Demonstration of
the compatibility of Escherichia coli (E. coli) and Legionella
pneumophila (Lp) antibodies with
the PB–GaAs platform compared to the results obtained with
conventional biosensing architectures developed for GaAs indicates
the attractive potential for operation of a sensitive biosensor. Furthermore,
these results showed that by carefully choosing the nature and preparation
methodology of a PB–GaAs interface, it is possible to effectively
tune the affinity of PB–GaAs-based sensors toward E. coli and Lp antibodies ultimately demonstrating
the superior specificity of the developed biosensing platform.