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Protein‐responsive imprinted polymers with specific shrinking and rebinding
Author(s) -
Chen Zhiyong,
Hua Zhendong,
Xu Li,
Huang Yong,
Zhao Meiping,
Li Yuanzong
Publication year - 2008
Publication title -
journal of molecular recognition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.401
H-Index - 79
eISSN - 1099-1352
pISSN - 0952-3499
DOI - 10.1002/jmr.870
Subject(s) - methacrylic acid , lysozyme , molecularly imprinted polymer , polymer , monomer , hydrogen bond , molecular imprinting , acrylamide , copolymer , chemistry , protein adsorption , adsorption , polymer chemistry , materials science , chemical engineering , biophysics , organic chemistry , molecule , biochemistry , selectivity , engineering , catalysis , biology
Stimuli‐responsive protein imprinted polymers were obtained via a combination of molecular imprinting and reversible stimuli‐responsive polymer using lysozyme or cytochrome c as template, N ‐isopropylacrylamide (NIPA) as major monomer, methacrylic acid (MAA) and acrylamide (AAm) as functional co‐monomers, and N , N ‐methylenebisacrylamide (MBAAm) as crosslinker. The molecularly imprinted polymers (MIPs) can respond not only to external stimuli such as temperature and salt concentration, but also to the corresponding template protein with significant specific volume shrinking. This specific shrinking behavior was attributed to the synergistic effect of multiple‐site weak interactions (electrostatic force, hydrogen bonding and hydrophobic interaction) and the cavity effect. The MIPs showed highly selective adsorption of template proteins with specific shrinking compared with the non‐imprinted polymers. The results indicated that the MIPs seemed to change shape to accommodate the conformation of the template protein leading to the formation of a shape complementary cavity. Copyright © 2008 John Wiley & Sons, Ltd.