{Reference Type}: Journal Article
{Title}: A Strep-tag Imprinted Polymer Platform for Heterogenous Bio(electro)catalysis.
{Author}: Yarman A;Waffo AFT;Katz S;Bernitzky CCM;Kovács N;Borrero P;Frielingsdorf S;Supala E;Dragelj J;Kurbanoglu S;Neumann B;Lenz O;Gyurcsányi RE;Mroginski MA;Wollenberger U;Scheller FW;Caserta G;Zebger I;
{Journal}: Angew Chem Int Ed Engl
{Volume}: 0
{Issue}: 0
{Year}: 2024 Jul 9
{Factor}: 16.823
{DOI}: 10.1002/anie.202408979
{Abstract}: Molecularly imprinted polymers (MIPs) are artificial receptors equipped with selective recognition sites for target molecules. One of the most promising-strategies for protein MIPs relies on the exploitation of short surface-exposed protein fragments, termed epitopes, as templates to imprint binding sites in a polymer scaffold for a desired protein. However, the lack of high-resolution structural data of flexible surface-exposed regions challenges the selection of suitable epitopes. Here, we addressed this drawback by developing a polyscopoletin-based MIP that recognizes recombinant proteins via the widely used Strep-tag II affinity peptide. Electrochemistry, surface-sensitive spectroscopy, and molecular dynamics simulations were employed to ensure an utmost control of the Strep-MIP electrosynthesis. The functionality of this novel platform was verified with two Strep-tag labeled enzymes: an O2-tolerant [NiFe]-hydrogenase, and an alkaline phosphatase. The enzymes preserved their biocatalytic activities after multiple utilization confirming the efficiency of Strep-MIP as a general biocompatible platform to confine recombinant proteins for exploitation in biotechnology.