Recognition, Neutralization, and Clearance of Target Peptides in the Bloodstream of Living Mice by Molecularly Imprinted Polymer Nanoparticles: A Plastic Antibody
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Hoshino, Yu
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Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USAUniv Calif Irvine, Dept Chem, Irvine, CA 92697 USA
Hoshino, Yu
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Koide, Hiroyuki
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Urakami, Takeo
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Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, Shizuoka 4228526, JapanUniv Calif Irvine, Dept Chem, Irvine, CA 92697 USA
Urakami, Takeo
[2
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Kanazawa, Hiroaki
[3
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Kodama, Takashi
[4
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Oku, Naoto
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Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, Shizuoka 4228526, JapanUniv Calif Irvine, Dept Chem, Irvine, CA 92697 USA
Oku, Naoto
[2
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Shea, Kenneth J.
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Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USAUniv Calif Irvine, Dept Chem, Irvine, CA 92697 USA
Shea, Kenneth J.
[1
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机构:
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, Shizuoka 4228526, Japan
We report that simple, synthetic organic polymer nanoparticles (NPs) can capture and clear a target peptide toxin in the bloodstream of living mice. The protein-sized polymer nanoparticles, with a binding affinity and selectivity comparable to those of natural antibodies, were prepared by combining a functional monomer optimization strategy with molecular-imprinting nanoparticle synthesis. As a result of binding and removal of melittin by NPs in vivo, the mortality and peripheral toxic symptoms due to melittin were significantly diminished. In vivo imaging of the polymer nanoparticles (or "plastic antibodies") established that the NPs accelerate clearance of the peptide from blood and accumulate in the liver. Coupled with their biocompatibility and nontoxic characteristics, plastic antibodies offer the potential for neutralizing a wide range of biomacromolecules in vivo.