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Site-selective immobilization of streptavidin on enzymatically biotinylated bacterial magnetic particles

机译:链霉亲和素在酶促生物素化细菌磁性颗粒上的定点固定

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Biotinylated magnetic nanoparticles were constructed by displaying biotin acceptor peptide (BAP) on the surfaces of bacterial magnetic particles (BacMPs) synthesized by Magneto spirillum magneticum AMB-1. Both BAP and green fluorescent protein (GFP) were fused to Mms13 that was isolated from BacMP membranes. The localization of the fusion protein, BAP-Mms13-GFP, was confirmed by fluorescence analysis. BacMPs that expressed BAP-Mms13-GFP (BAP/GFP-BacMPs) were extracted from bacterial cells and incubated with biotin and Escherichia coli biotin ligase. The in vitro biotinylation of BAP/GFP-BacMPs was confirmed using alkaline phosphatase (ALP)-labeled streptavidin. The conjugation system developed in this study provides a method for producing biotin- or streptavidin-labeled magnetic nanoparticles without the use of a crosslinker reagent. Various functional materials can be immobilized site-selectively onto these uniquely designed BacMPs. By combining this site-selective biotinylation technology and protein display methodology, increasingly innovative and attractive magnetic nano-materials can be constructed.
机译:通过将生物素受体肽(BAP)展示在由Magneto spirillum magneticum AMB-1合成的细菌磁性颗粒(BacMP)的表面上来构建生物素化的磁性纳米颗粒。 BAP和绿色荧光蛋白(GFP)都与从BacMP膜分离的Mms13融合。通过荧光分析证实了融合蛋白BAP-Mms13-GFP的定位。从细菌细胞中提取表达BAP-Mms13-GFP(BAP / GFP-BacMPs)的BacMP,并与生物素和大肠杆菌生物素连接酶孵育。使用碱性磷酸酶(ALP)标记的链霉亲和素可以证实BAP / GFP-BacMPs的体外生物素化。在这项研究中开发的偶联系统提供了一种无需使用交联剂即可生产生物素或链霉亲和素标记的磁性纳米颗粒的方法。可以将各种功能材料选择性地固定在这些独特设计的BacMP上。通过将这种位点选择性生物素化技术与蛋白质展示方法相结合,可以构建出日益创新和有吸引力的磁性纳米材料。

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