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• W2268689553 endingPage "190" @default.
• W2268689553 startingPage "179" @default.
• W2268689553 abstract "Molecularly imprinted polymers (MIPs) for the recognition of proteins are expected to possess high affinity through the establishment of multiple interactions between the polymer matrix and the large number of functional groups of the target. However, while highly affine recognition sites need building blocks rich in complementary functionalities to their target, such units are likely to generate high levels of non-specific binding. This paradox, that nature solved by evolution for biological receptors, needs to be addressed by the implementation of new concepts in molecular imprinting of proteins. Additionally, the structural variability, large size and incompatibility with a range of monomers made the development of protein MIPs to take a slow start. While the majority of MIP preparation methods are variants of chemical polymerization, the polymerization of electroactive functional monomers emerged as a particularly advantageous approach for chemical sensing application. Electropolymerization can be performed from aqueous solutions to preserve the natural conformation of the protein templates, with high spatial resolution and electrochemical control of the polymerization process. This review compiles the latest results, identifying major trends and providing an outlook on the perspectives of electrosynthesised protein-imprinted MIPs for chemical sensing." @default.
• W2268689553 created "2016-06-24" @default.
• W2268689553 creator A5007527159 @default.
• W2268689553 creator A5022203074 @default.
• W2268689553 creator A5024640881 @default.
• W2268689553 creator A5037893812 @default.
• W2268689553 creator A5058663837 @default.
• W2268689553 date "2016-05-01" @default.
• W2268689553 modified "2023-10-18" @default.
• W2268689553 title "Electrosynthesized molecularly imprinted polymers for protein recognition" @default.
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