Kachel Volker, Sindelar Georg, Grimm Stefan
Max-Planck-Institute for Biochemistry, Am Klopferspitz 18a, 82152 Martinsried, Germany.
BMC Biotechnol. 2006 Feb 16;6:9. doi: 10.1186/1472-6750-6-9.
With the availability of complete genomes, a systematic inventory of cellular processes becomes achievable. This requires assessing the function of all individual genes. Transfection of plasmid DNA into cell culture cells is an essential technique for this aim as it allows functional overexpression or downregulation of genes. While many robotic systems isolate plasmids for sequencing purposes, for more demanding applications such as transfections there is a shortage of robots for the high-throughput isolation of plasmid DNA.
Here we describe a custom-made, automated device, which uses a special protocol to isolate plasmid DNAs with a purity sufficient for efficient transfections into mammalian cells. Approximately 1,600 ultra pure plasmids can be isolated in a 96-well plate format within 12 hours. As a unique feature the robot comprises the integration of a centrifuge instead of expensive columns, the use of a custom-made pipetting head with a movable gripper, especially designed shaking platforms and an acetone wash facility.
Using this robot we demonstrate how centrifugation steps with multiple precipitations, most notably through a precipitation step of SDS in isopropanol, lead to high purity plasmid DNA and make possible high-throughput transfections into mammalian cells for functional gene annotations.
随着完整基因组的可得性,对细胞过程进行系统编目成为可能。这需要评估所有单个基因的功能。将质粒DNA转染到细胞培养细胞中是实现这一目标的一项基本技术,因为它允许基因的功能性过表达或下调。虽然许多机器人系统用于分离质粒以进行测序,但对于诸如转染等要求更高的应用,用于高通量分离质粒DNA的机器人却很短缺。
在此我们描述了一种定制的自动化设备,它使用一种特殊方案来分离纯度足以高效转染哺乳动物细胞的质粒DNA。在12小时内可以以96孔板形式分离出约1600个超纯质粒。该机器人的独特之处在于集成了一台离心机而非昂贵的柱子,使用了带有可移动夹具的定制移液器头、特别设计的振荡平台和丙酮洗涤装置。
使用该机器人,我们展示了多次沉淀的离心步骤,尤其是通过异丙醇中SDS沉淀步骤,如何产生高纯度质粒DNA,并使对哺乳动物细胞进行高通量转染以进行功能基因注释成为可能。