Synthetic Polymer Nanoparticles with Antibody-like Affinity for a Hydrophilic Peptide

被引:107
作者
Zeng, Zhiyang [1 ]
Hoshino, Yu [1 ]
Rodriguez, Andy [1 ]
Yoo, Hoseong [1 ]
Shea, Kenneth J. [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
selective peptide capture; synthetic nanoparticles; molecular imprinting; QCM; inverse microemulsion polymerization; plastic antibodies; INVERSE MICROEMULSION POLYMERIZATION; RECOGNITION; MICROGELS; PROTEINS; BINDING; PH;
D O I
10.1021/nn901256s
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic polymer nanoparticles with antibody-like affinity for a hydrophilic peptide have been prepared by inverse microemulsion polymerization. Peptide affinity was achieved in part by incorporating the target (imprint) peptide in the polymerization reaction mixture. Incorporation of the imprint peptide assists in the creation of complementary binding sites in the resulting polymer nanoparticle (NP). To orient the imprint peptide at the interface of the water and oil domains during polymerization, the peptide target was coupled with fatty acid chains of varying length. The peptide-NP binding affinities (ca. 90-900 nM) were quantitatively evaluated by a quartz crystal microbalance (QCM). The optimal chain length was established that created high affinity peptide binding sites on the surface of the nanoparticles. This method can be used for the preparation of nanosized synthetic polymers with antibody-like affinity for hydrophilic peptides and proteins ("plastic antibodies").
引用
收藏
页码:199 / 204
页数:6
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