...
首页> 外文期刊>Biotechnology and Bioengineering >Magnetic cell separation using nano-sized bacterial magnetic particles with reconstructed magnetosome membrane
【24h】

Magnetic cell separation using nano-sized bacterial magnetic particles with reconstructed magnetosome membrane

机译:使用纳米细菌磁性粒子和重构的磁小体膜进行磁细胞分离

获取原文
获取原文并翻译 | 示例
           

摘要

Magnetic nanoparticles produced by magnetotactic bacterium, bacterial magnetic particles (BacMPs), covered with it lipid bilayer membrane (magnetosome membrane) can be used to separate specific target cells from heterogeneous mixtures because they are easily manipulated by magnets and it is easy to display functional proteins on their surface via genetic engineering. Despite possessing unique and valuable characteristics, the potential toxicity of BacMPs to the separated cells has not been characterized in detail. Here, a novel technique was developed for the reconstruction of magnetosome membrane of BacMPs expressing protein A (protein A-BacMPs) to reduce cytotoxicity and the newly developed nanomaterial was then used for magnetic cell separation. The development of the magnetosome membrane-reconstructed protein A-BacMP was based on the characteristics of the Mms13 anchor protein, which strongly binds to the magnetite surface of BacMPs. Treatment of protein A-BacMPs with detergents removed contaminating protein but did not affect retention of Mms13-protein A fusion proteins. The particle surfaces were then reconstructed with phosphatidylcholine. The protein A-BacMPs containing reconstructed magnetosome membranes remained dispersible and retained the ability to immobilize antibody. In addition, they contained few membrane surface proteins and endotoxins, which were observed on non-treated protein A-BacMPs. Magnetic separation of monocytes and B-lymphocytes from the peripheral blood was achieved with high purity using magnetosome membrane-reconstructed protein A-BacMPs.
机译:由趋磁细菌产生的磁性纳米颗粒,覆盖有脂质双层膜(磁性体膜)的细菌磁性颗粒(BacMPs)可用于从异质混合物中分离特定的靶细胞,因为它们易于被磁体操纵并且易于展示功能性蛋白通过基因工程在他们的表面。尽管具有独特和有价值的特性,但尚未详细描述BacMP对分离细胞的潜在毒性。在这里,开发了一种新的技术来重建表达蛋白A(蛋白A-BacMPs)的BacMPs的核小体膜,以减少细胞毒性,然后将新开发的纳米材料用于磁性细胞分离。磁小体膜重建蛋白A-BacMP的开发基于Mms13锚定蛋白的特征,该蛋白牢固地结合到BacMPs的磁铁矿表面。用去污剂处理蛋白A-BacMPs去除了污染蛋白,但不影响Mms13-蛋白A融合蛋白的保留。然后用磷脂酰胆碱重建颗粒表面。包含重构的磁小体膜的蛋白A-BacMP保持可分散性,并保留了固定抗体的能力。此外,它们几乎不包含膜表面蛋白和内毒素,这在未处理的蛋白A-BacMPs上观察到。使用磁小体膜重构蛋白A-BacMPs,可以实现高纯度的单核细胞和B淋巴细胞与外周血的磁分离。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号