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Magnetic separation of CD14(+) cells using antibody binding with protein A expressed on bacterial magnetic particles for generating dendritic cells

机译:使用与细菌磁性颗粒上表达的蛋白A结合的抗体结合的CD14(+)细胞磁分离产生树突状细胞

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Herein the potential of a highly efficient cell separation system using bacterial magnetic particles expressing protein A (protein A-Bac-MPs) was demonstrated. Protein A was expressed on BacMPs using the transmembrane proteins Mms13 and MagA as anchor molecules. The evaluations of the numbers of bound antibody molecules and binding capabilities of the protein A-BacMPs using Mms13 indicated that the antibodies were efficiently introduced into protein A-BacMPs using Mms13 in comparison to MagA. In addition, the recovery ratio of the target cells on the magnetic cell separation system was enhanced by using protein A-BacMPs with Mms13. Using positive selection against peripheral blood mononuclear cells, the CD14(+) cells were separated at a purity of more than 99% by protein A-BacNlPs using Mms13. Furthermore, in the evaluation of the influence of protein A-BacMPs on the separated cells, the CD14(+) cells separated using protein A-BacMPs and were successfully differentiated into dendritic cells. (c) 2006 Elsevier Inc. All rights reserved.
机译:本文证明了使用表达蛋白质A(蛋白质A-Bac-MPs)的细菌磁性颗粒的高效细胞分离系统的潜力。使用跨膜蛋白Mms13和MagA作为锚分子在BacMP上表达蛋白A。使用Mms13评估结合的抗体分子数量和蛋白A-BacMP的结合能力表明,与MagA相比,使用Mms13将抗体有效地引入了蛋白A-BacMPs。此外,通过使用具有Mms13的蛋白A-BacMPs,可以提高磁性细胞分离系统上靶细胞的回收率。使用针对外周血单核细胞的阳性选择,使用Mms13通过蛋白A-BacNlPs分离CD14(+)细胞,纯度超过99%。此外,在评估蛋白A-BacMPs对分离细胞的影响时,使用蛋白A-BacMPs分离的CD14(+)细胞已成功分化为树突状细胞。 (c)2006 Elsevier Inc.保留所有权利。

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