Development and Optimization of a Process for Automated Recovery of Single Cells Identified by Microengraving

被引:59
作者
Choi, Jae Hyeok [1 ,2 ]
Ogunniyi, Adebola O. [1 ]
Du, Mindy [1 ]
Du, Minna [1 ]
Kretschmann, Marcel [3 ]
Eberhardt, Jens [3 ]
Love, J. Christopher [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Whitehead Inst Biomed Res, Cambridge, MA 02139 USA
[3] AVISO GmbH, D-07747 Jena, Germany
关键词
automation; high-throughput screening; clonal selection; monoclonal antibody; HUMAN MONOCLONAL-ANTIBODIES; SURFACE DISPLAY; MICROFLUIDIC PLATFORM; MAMMALIAN-CELLS; B-CELLS; LIBRARIES; CHIP; ANTIGENS;
D O I
10.1002/btpr.374
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Microfabricated devices are useful tools for manipulating and interrogating large numbers of single cells in a rapid and cost-effective manner, but connecting these systems to the existing platforms used in routine high-throughput screening of libraries of cells remains challenging. Methods to sort individual cells of interest from custom microscale devices to standardized culture dishes in an efficient and automated manner without affecting the viability of the cells are critical. Combining a commercially available instrument for colony picking (CellCelector, AVISO GmbH) and a customized software module, we have established an optimized process for the automated retrieval of individual antibody-producing cells, secreting desirable antibodies, from dense arrays of subnanoliter containers. The selection of cells for retrieval is guided by data obtained from a high-throughput, single-cell screening method called microengraving. Using this system, 100 clones from a mixed population of two cell lines secreting different antibodies (12CA5 and HY8099-01) were sorted with 100% accuracy (50 clones of each) in similar to 2 h, and the cells retained viability. (C) 2010 American Institute of Chemical Engineers Biotechnol. Prog., 26: 888-895, 2010
引用
收藏
页码:888 / 895
页数:8
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