Molecularly imprinted polymers are ideal alternatives to natural recognition elements for a variety of reasons, including facile synthesis, greater chemical and long term stability, and reusability. One of the most challenging tasks in developing such polymers is provide them of a signal transduction capability, enabling to respond to a specific binding event. In this thesis, protein-imprinted polymers, capable of specific transduction of binding event into a fluorescence change were prepared using an assistant-peptide bearing an environment-sensitive fluorophore. The preparation has included the synthesis of the environment-sensitive peptide and subsequent incorporation into the polymer network through the imprinting process. Binding studies proved that MIP-SA-allyl-peptide has large absorption capacity and good affinity and selectivity toward BSA when compared with pure MIP. The greater binding properties of MIP-SA-allyl-peptide were found to derive from the assistant-peptide that suitably oriented into the cavity, acts as binding site in cooperation with the imprinted cavity. Furthermore, transduction signaling studies proved that MIP-SA-allyl-dansyl-peptide is able to detect and report the protein binding into a precise detection range. The proposed fluorescent-imprinted polymer provides a new and general strategy for protein-sensing platforms and opens up to the field of biosensors.

Molecularly imprinted polymers with assistant recognition biomolecule for protein detection

2015

Abstract

Molecularly imprinted polymers are ideal alternatives to natural recognition elements for a variety of reasons, including facile synthesis, greater chemical and long term stability, and reusability. One of the most challenging tasks in developing such polymers is provide them of a signal transduction capability, enabling to respond to a specific binding event. In this thesis, protein-imprinted polymers, capable of specific transduction of binding event into a fluorescence change were prepared using an assistant-peptide bearing an environment-sensitive fluorophore. The preparation has included the synthesis of the environment-sensitive peptide and subsequent incorporation into the polymer network through the imprinting process. Binding studies proved that MIP-SA-allyl-peptide has large absorption capacity and good affinity and selectivity toward BSA when compared with pure MIP. The greater binding properties of MIP-SA-allyl-peptide were found to derive from the assistant-peptide that suitably oriented into the cavity, acts as binding site in cooperation with the imprinted cavity. Furthermore, transduction signaling studies proved that MIP-SA-allyl-dansyl-peptide is able to detect and report the protein binding into a precise detection range. The proposed fluorescent-imprinted polymer provides a new and general strategy for protein-sensing platforms and opens up to the field of biosensors.
2015
it
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/315439
Il codice NBN di questa tesi è URN:NBN:IT:BNCF-315439