Lysozyme-imprinted polymer synthesized using UV free-radical polymerization

Molecular imprinting is a method to fabricate a polymeric material (molecularly imprinted polymer or MIP) capable of selectively recognizing template molecules Molecular imprinting of small molecules has been studied widely Less common however is the imprinting of biological macromolecules including proteins among which lysozyme is an important molecule in the food pharmaceutical and diagnostic sciences In this study lysozyme MIP was fabricated in two steps First lysozyme PEG600DMA and methacrylic acid were used as the template molecule cross-linking monomer and the functional monomer respectively in a UV free-radical polymerization process to synthesize a polymeric gel Second lysozyme was removed by enzymatic digestion Non-imprinted polymer (NIP) was synthesized without lysozyme addition To evaluate the preferential binding capability of MIP lysozyme RNase A or a 50 50 mixture of lysozyme and RNase A was added to MIP and NIP and then released by digestion It was found that when more lysozyme was added to the reaction mixture the quantity of protein released from the polymer increased reflecting more potential binding sites Tests of MIP with a competitive binding mixture of lysozyme and RNase A showed the MIP preferentially bound a greater amount of lysozyme up to 20 times more than RNase A NIP bound only small amounts of both proteins and did not show a preference for binding either lysozyme or RNase A These results demonstrate that lysozyme was successfully imprinted into the MIP by UV free-radical polymerization and the fabricated MIP was able to preferentially bind its template protein (C) 2010 Elsevier B V All rights reserved