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Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging
Regulatory authorities require that cell lines used in commercial production of recombinant proteins must be derived from a single cell progenitor or clone. The limiting dilution method of cell cloning required multiple rounds of low‐density cell plating and microscopic observation of a single cell...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054913/ https://www.ncbi.nlm.nih.gov/pubmed/26195345 http://dx.doi.org/10.1002/btpr.2145 |
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author | Evans, Krista Albanetti, Thomas Venkat, Raghavan Schoner, Ronald Savery, James Miro‐Quesada, Guillermo Rajan, Bhargavi Groves, Christopher |
author_facet | Evans, Krista Albanetti, Thomas Venkat, Raghavan Schoner, Ronald Savery, James Miro‐Quesada, Guillermo Rajan, Bhargavi Groves, Christopher |
author_sort | Evans, Krista |
collection | PubMed |
description | Regulatory authorities require that cell lines used in commercial production of recombinant proteins must be derived from a single cell progenitor or clone. The limiting dilution method of cell cloning required multiple rounds of low‐density cell plating and microscopic observation of a single cell in order to provide evidence of monoclonality. Other cloning methods rely on calculating statistical probability of monoclonality rather than visual microscopic observation of cells. We have combined the single cell deposition capability of the Becton Dickinson Influx™ cell sorter with the microscopic imaging capability of the SynenTec Cellavista to create a system for producing clonal production cell lines. The efficiency of single cell deposition by the Influx™ was determined to be 98% using fluorescently labeled cells. The centrifugal force required to settle the deposited cells to the bottom of the microplate well was established to be 1,126g providing a 98.1% probability that all cells will be in the focal plane of the Cellavista imaging system. The probability that a single cell was deposited by the cell sorter combined with the probability of every cell settling into the focal plane of the imager yield a combined >99% probability of documented monoclonality. © 2015 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers Biotechnol. Prog., 31:1172–1178, 2015 |
format | Online Article Text |
id | pubmed-5054913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50549132016-10-19 Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging Evans, Krista Albanetti, Thomas Venkat, Raghavan Schoner, Ronald Savery, James Miro‐Quesada, Guillermo Rajan, Bhargavi Groves, Christopher Biotechnol Prog SPECIAL SECTION: Articles presented at the Cell Culture Engineering XIV (CCE XIV) conference, Québec city, Canada, May 4–9, 2014 Regulatory authorities require that cell lines used in commercial production of recombinant proteins must be derived from a single cell progenitor or clone. The limiting dilution method of cell cloning required multiple rounds of low‐density cell plating and microscopic observation of a single cell in order to provide evidence of monoclonality. Other cloning methods rely on calculating statistical probability of monoclonality rather than visual microscopic observation of cells. We have combined the single cell deposition capability of the Becton Dickinson Influx™ cell sorter with the microscopic imaging capability of the SynenTec Cellavista to create a system for producing clonal production cell lines. The efficiency of single cell deposition by the Influx™ was determined to be 98% using fluorescently labeled cells. The centrifugal force required to settle the deposited cells to the bottom of the microplate well was established to be 1,126g providing a 98.1% probability that all cells will be in the focal plane of the Cellavista imaging system. The probability that a single cell was deposited by the cell sorter combined with the probability of every cell settling into the focal plane of the imager yield a combined >99% probability of documented monoclonality. © 2015 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers Biotechnol. Prog., 31:1172–1178, 2015 John Wiley and Sons Inc. 2015-09-18 2015 /pmc/articles/PMC5054913/ /pubmed/26195345 http://dx.doi.org/10.1002/btpr.2145 Text en © 2015 American Institute of Chemical Engineers This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/3.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | SPECIAL SECTION: Articles presented at the Cell Culture Engineering XIV (CCE XIV) conference, Québec city, Canada, May 4–9, 2014 Evans, Krista Albanetti, Thomas Venkat, Raghavan Schoner, Ronald Savery, James Miro‐Quesada, Guillermo Rajan, Bhargavi Groves, Christopher Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
title | Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
title_full | Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
title_fullStr | Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
title_full_unstemmed | Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
title_short | Assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
title_sort | assurance of monoclonality in one round of cloning through cell sorting for single cell deposition coupled with high resolution cell imaging |
topic | SPECIAL SECTION: Articles presented at the Cell Culture Engineering XIV (CCE XIV) conference, Québec city, Canada, May 4–9, 2014 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054913/ https://www.ncbi.nlm.nih.gov/pubmed/26195345 http://dx.doi.org/10.1002/btpr.2145 |
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