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Direct Magnetic Separation of Immune Cells from Whole Blood Using Bacterial Magnetic Particles Displaying Protein G

机译:使用显示蛋白质G的细菌磁性粒子从全血中直接免疫分离免疫细胞

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Direct separation of target cells from mixed population,such as peripheral blood,umbilical cord blood,and bone marrow,is an essential technique for various therapeutic or diagnosis applications.In this study,novel particles were fabricated,and direct magnetic separation of immune cells from whole blood using such particles was performed.The mag-netotactic bacterium Magnetospirillum magneticum AMB-1 synthesizes intracellular bacterial magnetic particles(BacMPs),and protein G was expressed on the surface of the BacMPs by gene fusion techniques with anchor proteins isolated from BacMP membrane.The BacMPs displaying protein G(protein G-BacMPs)had high binding capabilities to a wide range of antibody types,and various versions of protein G-BacMPs binding with different anti-CD monoclonal antibodies were constructed.Consequently,direct magnetic separation of immune cells from whole blood using protein G-BacMPs binding with anti-CD monoclonal antibodies was demonstrated.B lymphocytes(CD19~+ cells)or T lymphocytes(CD3~+ cells),which represent less than 0.05% in whole blood cells,were successfully separated at a purity level of more than 96%.This level was superior to that from previous reports using other magnetic separation approaches.The results of this study demonstrate the utility of protein G-BacMP and this particle may become a powerful tool for various therapeutic or diagnosis applications.
机译:从混合人群(如外周血,脐带血和骨髓)中直接分离靶细胞是用于各种治疗或诊断应用的必不可少的技术。在本研究中,制备了新颖的颗粒,并从中直接磁分离免疫细胞。磁致趋磁细菌Magnetospirillum magneticum AMB-1合成细胞内细菌磁颗粒(BacMPs),并通过基因融合技术与BacMP膜分离的锚定蛋白在BacMPs的表面表达G蛋白。展示蛋白G的BacMP具有与多种抗体类型的高结合能力,构建了与不同抗CD单克隆抗体结合的蛋白G-BacMP多种版本。因此,直接磁分离免疫细胞通过与抗CD单克隆抗体结合的G-BacMPs蛋白从全血中分离出B淋巴细胞(CD19〜+ c或T淋巴细胞(CD3〜+细胞)在全血细胞中所占比例不到0.05%,已成功分离出纯度超过96%的纯度,这一水平优于以前使用其他磁性分离方法的报道这项研究的结果证明了蛋白G-BacMP的实用性,该颗粒可能成为各种治疗或诊断应用的有力工具。

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