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High-throughput isolation of ultra-pure plasmid DNA by a robotic system

BACKGROUND: 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 ove...

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Autores principales: Kachel, Volker, Sindelar, Georg, Grimm, Stefan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1395312/
https://www.ncbi.nlm.nih.gov/pubmed/16483377
http://dx.doi.org/10.1186/1472-6750-6-9
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author Kachel, Volker
Sindelar, Georg
Grimm, Stefan
author_facet Kachel, Volker
Sindelar, Georg
Grimm, Stefan
author_sort Kachel, Volker
collection PubMed
description BACKGROUND: 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. RESULTS: 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. CONCLUSION: 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.
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spelling pubmed-13953122006-03-09 High-throughput isolation of ultra-pure plasmid DNA by a robotic system Kachel, Volker Sindelar, Georg Grimm, Stefan BMC Biotechnol Methodology Article BACKGROUND: 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. RESULTS: 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. CONCLUSION: 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. BioMed Central 2006-02-16 /pmc/articles/PMC1395312/ /pubmed/16483377 http://dx.doi.org/10.1186/1472-6750-6-9 Text en Copyright © 2006 Kachel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Kachel, Volker
Sindelar, Georg
Grimm, Stefan
High-throughput isolation of ultra-pure plasmid DNA by a robotic system
title High-throughput isolation of ultra-pure plasmid DNA by a robotic system
title_full High-throughput isolation of ultra-pure plasmid DNA by a robotic system
title_fullStr High-throughput isolation of ultra-pure plasmid DNA by a robotic system
title_full_unstemmed High-throughput isolation of ultra-pure plasmid DNA by a robotic system
title_short High-throughput isolation of ultra-pure plasmid DNA by a robotic system
title_sort high-throughput isolation of ultra-pure plasmid dna by a robotic system
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1395312/
https://www.ncbi.nlm.nih.gov/pubmed/16483377
http://dx.doi.org/10.1186/1472-6750-6-9
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