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A polymer nanoparticle with engineered affinity for a vascular endothelial growth factor (VEGF165).
Koide, Hiroyuki; Yoshimatsu, Keiichi; Hoshino, Yu; Lee, Shih-Hui; Okajima, Ai; Ariizumi, Saki; Narita, Yudai; Yonamine, Yusuke; Weisman, Adam C; Nishimura, Yuri; Oku, Naoto; Miura, Yoshiko; Shea, Kenneth J.
Afiliação
  • Koide H; Department of Medical Biochemistry, Graduate Division of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, Shizuoka 422-8526, Japan.
  • Yoshimatsu K; Department of Chemistry, University of California Irvine, Irvine, California 92697, USA.
  • Hoshino Y; Department of Chemistry, University of California Irvine, Irvine, California 92697, USA.
  • Lee SH; Department of Chemical Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395, Japan.
  • Okajima A; Department of Chemistry, University of California Irvine, Irvine, California 92697, USA.
  • Ariizumi S; Department of Medical Biochemistry, Graduate Division of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, Shizuoka 422-8526, Japan.
  • Narita Y; Department of Medical Biochemistry, Graduate Division of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, Shizuoka 422-8526, Japan.
  • Yonamine Y; Department of Medical Biochemistry, Graduate Division of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, Shizuoka 422-8526, Japan.
  • Weisman AC; Department of Chemistry, University of California Irvine, Irvine, California 92697, USA.
  • Nishimura Y; Department of Chemistry, University of California Irvine, Irvine, California 92697, USA.
  • Oku N; Department of Chemical Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395, Japan.
  • Miura Y; Department of Medical Biochemistry, Graduate Division of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka, Shizuoka 422-8526, Japan.
  • Shea KJ; Department of Chemical Engineering, Kyushu University, 744 Motooka, Fukuoka 819-0395, Japan.
Nat Chem ; 9(7): 715-722, 2017 07.
Article em En | MEDLINE | ID: mdl-28644480
ABSTRACT
Protein affinity reagents are widely used in basic research, diagnostics and separations and for clinical applications, the most common of which are antibodies. However, they often suffer from high cost, and difficulties in their development, production and storage. Here we show that a synthetic polymer nanoparticle (NP) can be engineered to have many of the functions of a protein affinity reagent. Polymer NPs with nM affinity to a key vascular endothelial growth factor (VEGF165) inhibit binding of the signalling protein to its receptor VEGFR-2, preventing receptor phosphorylation and downstream VEGF165-dependent endothelial cell migration and invasion into the extracellular matrix. In addition, the NPs inhibit VEGF-mediated new blood vessel formation in Matrigel plugs in vivo. Importantly, the non-toxic NPs were not found to exhibit off-target activity. These results support the assertion that synthetic polymers offer a new paradigm in the search for abiotic protein affinity reagents by providing many of the functions of their protein counterparts.
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Polímeros / Engenharia de Proteínas / Fator A de Crescimento do Endotélio Vascular / Nanopartículas Limite: Humans Idioma: En Revista: Nat Chem Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Polímeros / Engenharia de Proteínas / Fator A de Crescimento do Endotélio Vascular / Nanopartículas Limite: Humans Idioma: En Revista: Nat Chem Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão