Suppr超能文献

生物纳米技术中的水相兼容聚合物。

Aqueous compatible polymers in bionanotechnology.

作者信息

Carter S R, Rimmer S

机构信息

Department of Chemistry (Polymer Centre), University of Sheffield, Sheffield, South Yorkshire, S3 7HF, UK.

出版信息

IEE Proc Nanobiotechnol. 2005 Oct;152(5):169-76. doi: 10.1049/ip-nbt:20050007.

Abstract

Core-shell molecularly imprinted particles (CS-MIPs) have been synthesised using the technique of emulsion polymerisation with caffeine and theophylline being used in the surface template polymerisation with ethylene glycol dimethacrylate and oleylphenyl hydrogen phosphate. A radiolabelling study with caffeine-8-14C showed that the template was completely located at the particle surface during polymerisation. Caffeine could be specifically bound to a caffeine-imprinted CS-MIP to give a biphasic Scatchard binding curve, whereas the binding profile to a theophylline-imprinted CS-MIP was monophasic. The nanoparticles have the potential to be used in the molecular recognition of small molecules in a complex biological matrix. Water soluble highly-branched imidazole end-chain functionalised polymers of nanodimensions have also been synthesised via reversible addition-fragmentation chain transfer polymerisation. The polymers have lower critical solution temperatures which occur at sub-ambient temperatures and have proven useful in the affinity precipitation of proteins which are particularly temperature sensitive, e.g. the histidine-tagged protein fragment BRCA1. An overview of both of these areas of research is described outlining the diversity of these aqueous compatible polymers in molecular recognition processes at the nanoscale.

摘要

已采用乳液聚合法合成了核壳型分子印迹颗粒(CS-MIPs),在表面模板聚合过程中,使用咖啡因和茶碱与乙二醇二甲基丙烯酸酯和油基苯基磷酸氢酯。一项用咖啡因-8-14C进行的放射性标记研究表明,聚合过程中模板完全位于颗粒表面。咖啡因能特异性结合到咖啡因印迹的CS-MIP上,得到双相Scatchard结合曲线,而与茶碱印迹的CS-MIP的结合图谱是单相的。这些纳米颗粒有潜力用于复杂生物基质中小分子的分子识别。还通过可逆加成-断裂链转移聚合合成了纳米尺寸的水溶性高支化咪唑端链功能化聚合物。这些聚合物具有在低于环境温度时出现的较低临界溶液温度,并已证明可用于对温度特别敏感的蛋白质(如组氨酸标签蛋白片段BRCA1)的亲和沉淀。本文概述了这两个研究领域,概述了这些与水相容的聚合物在纳米级分子识别过程中的多样性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验