JPCB2010-Preparation and Recognition Properties of Bovine Hemoglobin.pdfVIP

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JPCB2010-Preparation and Recognition Properties of Bovine Hemoglobin.pdf

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JPCB2010-Preparation and Recognition Properties of Bovine Hemoglobin

Preparation and Recognition Properties of Bovine Hemoglobin Magnetic Molecularly Imprinted Polymers Xianwen Kan,?,? Qun Zhao,? Dalin Shao,? Zhirong Geng,? Zhilin Wang,*,? and Jun-Jie Zhu*,? State Key Laboratory of Coordination Chemistry, The Key Lab of Analytical chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing UniVersity, 22 Hankou Road, Nanjing 210093, People’s Republic of China, and Anhui Key Laboratory of Functional Molecular Solids, College of Chemistry and Materials Science, Anhui Normal UniVersity, Wuhu, 241000, People’s Republic of China ReceiVed: October 21, 2009; ReVised Manuscript ReceiVed: February 4, 2010 A simple method for the preparation of core-shell micro/nanostructured magnetic molecularly imprinted polymers (MIPs) for protein recognition is described. Magnetic MIPs were synthesized by copolymering γ-aminopropyltrimethoxysilane and tetraethyl orthosilicate at the surface of Fe3O4 nanospheres, which were directly covalently bound with template molecule, bovine hemoglobin (BHb), through imine bond. Transmission electron microscopy and scanning electron microscopy images showed that the Fe3O4 nanospheres with diameter about 50-150 nm were coated with the MIPs layer with average thickness about 10 nm, which enabled the magnetic MIPs to have a sensitive and fast magnetic response. The proximity between the thickness of MIPs layer and the spatial size of BHb indicated that the imprinted sites almost situated at the surface of magnetic MIPs, leading a rapid adsorption saturation within 1 h. And the adsorption amounts of magnetic MIPs toward BHb were estimated to be 10.52 mg/g at pH 6.5, which was 4.6 times higher than that of magnetic nonmolecularly imprinted polymers. Meanwhile, the result of selective test showed that the magnetic MIPs had an excellent recognition capacity to BHb compared to the other nontemplate proteins. Except for the spatial size complementary between BHb and the binding sites in magnetic MIPs, the