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开发并优化微刻痕识别的单细胞自动回收工艺。

Development and optimization of a process for automated recovery of single cells identified by microengraving.

机构信息

Dept. of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139.

出版信息

Biotechnol Prog. 2010 May-Jun;26(3):888-95. doi: 10.1002/btpr.374.

Abstract

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 HYB099-01) were sorted with 100% accuracy (50 clones of each) in approximately 2 h, and the cells retained viability.

摘要

微纳加工设备是一种非常有用的工具,可以快速、经济有效地操纵和检测大量的单细胞,但将这些系统与现有的高通量筛选细胞文库的平台相连接仍然具有挑战性。能够以高效、自动化的方式将感兴趣的单细胞从定制的微尺度设备中分拣到标准培养皿中,而不影响细胞活力,这一点至关重要。我们结合了一种商业上可用的集落挑选仪器(CellCelector,AVISO GmbH)和一个定制的软件模块,为从密集的亚纳升级容器阵列中自动检索分泌所需抗体的单个抗体产生细胞建立了一个优化的过程。细胞检索的选择是由一种称为微雕刻的高通量单细胞筛选方法获得的数据来指导的。使用该系统,在大约 2 小时内,可以 100%准确(每个 50 个克隆)地对来自分泌两种不同抗体(12CA5 和 HYB099-01)的两种细胞系的混合群体中的 100 个克隆进行分拣,并且细胞保持活力。

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