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A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology

Generating a highly productive cell line is resource intensive and typically involves long timelines because of the need to screen large numbers of candidates in protein production studies. This has led to miniaturization and automation strategies to allow for reductions in resources and higher thro...

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Autores principales: Le, Kim, Tan, Christopher, Gupta, Shivani, Guhan, Trupti, Barkhordarian, Hedieh, Lull, Jonathan, Stevens, Jennitte, Munro, Trent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585769/
https://www.ncbi.nlm.nih.gov/pubmed/30009534
http://dx.doi.org/10.1002/btpr.2690
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author Le, Kim
Tan, Christopher
Gupta, Shivani
Guhan, Trupti
Barkhordarian, Hedieh
Lull, Jonathan
Stevens, Jennitte
Munro, Trent
author_facet Le, Kim
Tan, Christopher
Gupta, Shivani
Guhan, Trupti
Barkhordarian, Hedieh
Lull, Jonathan
Stevens, Jennitte
Munro, Trent
author_sort Le, Kim
collection PubMed
description Generating a highly productive cell line is resource intensive and typically involves long timelines because of the need to screen large numbers of candidates in protein production studies. This has led to miniaturization and automation strategies to allow for reductions in resources and higher throughput. Current approaches rely on the use of standard cell culture vessels and bulky liquid handling equipment. New nanofludic technologies offer novel solutions to surpass these limits, further miniaturizing cell culture volumes (10(5) times smaller) by growing cells on custom nanofluidic chips. Berkeley Lights’ OptoElectro Positioning technology projects light patterns to activate photoconductors that gently repel cells to manipulate single cells on nanofluidic culturing chips. Using a fully integrated technology platform (Beacon), common cell culture tasks can be programmed through software, allowing maintenance and analysis of thousands of cell lines in parallel on a single chip. Here, we describe the ability to perform key cell line development work on the Beacon platform. We demonstrate that commercial production Chinese hamster ovary cell lines can be isolated, cultured, screened, and exported at high efficiency. We compare this process head to head with a FACS‐enabled microtiter plate‐based workflow and demonstrate generation of comparable clonal cell lines with reduced resources. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 34:1438–1446, 2018
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spelling pubmed-65857692019-06-27 A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology Le, Kim Tan, Christopher Gupta, Shivani Guhan, Trupti Barkhordarian, Hedieh Lull, Jonathan Stevens, Jennitte Munro, Trent Biotechnol Prog RESEARCH ARTICLES Generating a highly productive cell line is resource intensive and typically involves long timelines because of the need to screen large numbers of candidates in protein production studies. This has led to miniaturization and automation strategies to allow for reductions in resources and higher throughput. Current approaches rely on the use of standard cell culture vessels and bulky liquid handling equipment. New nanofludic technologies offer novel solutions to surpass these limits, further miniaturizing cell culture volumes (10(5) times smaller) by growing cells on custom nanofluidic chips. Berkeley Lights’ OptoElectro Positioning technology projects light patterns to activate photoconductors that gently repel cells to manipulate single cells on nanofluidic culturing chips. Using a fully integrated technology platform (Beacon), common cell culture tasks can be programmed through software, allowing maintenance and analysis of thousands of cell lines in parallel on a single chip. Here, we describe the ability to perform key cell line development work on the Beacon platform. We demonstrate that commercial production Chinese hamster ovary cell lines can be isolated, cultured, screened, and exported at high efficiency. We compare this process head to head with a FACS‐enabled microtiter plate‐based workflow and demonstrate generation of comparable clonal cell lines with reduced resources. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 34:1438–1446, 2018 John Wiley & Sons, Inc. 2018-09-19 2018 /pmc/articles/PMC6585769/ /pubmed/30009534 http://dx.doi.org/10.1002/btpr.2690 Text en © 2018 The Authors. Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle RESEARCH ARTICLES
Le, Kim
Tan, Christopher
Gupta, Shivani
Guhan, Trupti
Barkhordarian, Hedieh
Lull, Jonathan
Stevens, Jennitte
Munro, Trent
A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
title A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
title_full A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
title_fullStr A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
title_full_unstemmed A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
title_short A novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
title_sort novel mammalian cell line development platform utilizing nanofluidics and optoelectro positioning technology
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585769/
https://www.ncbi.nlm.nih.gov/pubmed/30009534
http://dx.doi.org/10.1002/btpr.2690
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