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Biologically Active Polymersomes from Amphiphilic Glycopeptides

机译:两亲性糖肽的生物活性多聚体

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摘要

Polypeptide block copolymers with different block length ratios were obtained by sequential ring-opening polymerization of benzyl-L-glutamate and prop-argylglycine (PG) N-carboxyanhydrides. Glycosylation of the poly(PG) block was obtained by Huisgens cyclo-addition "click" reaction using azide-functionalized gal-actose. All copolymers were self-assembled using the nanoprecipitation method to obtain spherical and worm-like micelles as well as polymersomes depending on the block length ratio and the nanoprecipitation conditions. These structures display bioactive galactose units in the polymersome shell, as proven by selective lectin binding experiments.
机译:通过连续的苄基-L-谷氨酸酯和炔丙基甘氨酸(PG)N-羧基酐的开环聚合反应,可以得到具有不同嵌段长度比的多肽嵌段共聚物。聚(PG)嵌段的糖基化是通过使用叠氮化物官能化的半乳糖通过Huisgens环加成的“点击”反应获得的。根据嵌段长度比和纳米沉淀条件,使用纳米沉淀法将所有共聚物自组装,以获得球形和蠕虫状的胶束以及聚合物囊泡。如选择性凝集素结合实验所证明的,这些结构在多聚体壳中显示出生物活性的半乳糖单元。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第1期|p.119-122|共4页
  • 作者单位

    School of Chemical Sciences, Dublin City University, Dublin 9, Ireland;

    Universite de Bordeaux/IPB, ENSCBP, 16 avenue Pey Berland, 33607 Pessac Cedex, France, and CNRS, Laboratoire de Chimie des Polymeres Organiques (UMR5629), Pessac, France;

    Universite de Bordeaux/IPB, ENSCBP, 16 avenue Pey Berland, 33607 Pessac Cedex, France, and CNRS, Laboratoire de Chimie des Polymeres Organiques (UMR5629), Pessac, France;

    Universite de Bordeaux/IPB, ENSCBP, 16 avenue Pey Berland, 33607 Pessac Cedex, France, and CNRS, Laboratoire de Chimie des Polymeres Organiques (UMR5629), Pessac, France;

    School of Chemical Sciences, Dublin City University, Dublin 9, Ireland,Technische Universiteit Eindhoven, Den Dolech 2, P.O. Box 513, 5600 MB Eindhoven, The Netherlands;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:13:20

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