Interfacial Molecular Imprinting for the Production of Immunoresponsive Materials
Traditionally, molecular imprinting of proteins has proved challenging due to solvent limitations, recovery of the protein template, and most importantly, lack of specificity due to the large number of possible interaction sites. In this work, a surface imprinting technique has been developed to template hydrogel materials for specific protein recognition. Our model protein, the immunoglobulin IgG, was a unique choice due to its conserved/variable structure. Use of this 150 kDa molecule allowed for experiments to separate imprinting effects due to shape, surface chemistry, and molecular orientation. A template mask was produced whereby protein (monoclonal IgG) was immobilized in a controlled orientation through a hydrazide reaction such that the antigen binding domains were fully exposed. A monomer mixture was brought in contact with this mask and polymerized to produce a surface imprinted hydrogel specific to the target protein. Non-imprinted, control materials were produced in the absence of protein. Imprinted hydrogels formed from the monomer 2-hydroxyethylmethacrylate and crosslinker ethylene glycol dimethacrylate bound significantly more IgG (monoclonal anti-c-myc) than the non-imprinted control materials. In addition, no significant binding was seen of a second immunoglobulin (anti-pig-IgG) by the imprinted gel, indicating specificity for the target protein.
Y. Zheng and D. Henthorn, "Interfacial Molecular Imprinting for the Production of Immunoresponsive Materials," US - Japan Joint Topical Conference on Medical Engineering, Drug Delivery Systems and Therapeutic Systems, American Institute of Chemical Engineers (AIChE), Jan 2006.
Chemical and Biochemical Engineering
Keywords and Phrases
Solvent Limitations; Molecular imprinting; Proteins
Article - Conference proceedings
© 2006 American Institute of Chemical Engineers (AIChE), All rights reserved.
01 Jan 2006