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Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development
Studying the biophysical characteristics of glycosylated proteins and solving their three-dimensional structures requires homogeneous recombinant protein of high quality.We introduce here a new approach to produce glycoproteins in homogenous form with the well-established, glycosylation mutant CHO L...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235087/ https://www.ncbi.nlm.nih.gov/pubmed/22174749 http://dx.doi.org/10.1371/journal.pone.0027829 |
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author | Wilke, Sonja Groebe, Lothar Maffenbeier, Vitali Jäger, Volker Gossen, Manfred Josewski, Jörn Duda, Agathe Polle, Lilia Owens, Raymond J. Wirth, Dagmar Heinz, Dirk W. van den Heuvel, Joop Büssow, Konrad |
author_facet | Wilke, Sonja Groebe, Lothar Maffenbeier, Vitali Jäger, Volker Gossen, Manfred Josewski, Jörn Duda, Agathe Polle, Lilia Owens, Raymond J. Wirth, Dagmar Heinz, Dirk W. van den Heuvel, Joop Büssow, Konrad |
author_sort | Wilke, Sonja |
collection | PubMed |
description | Studying the biophysical characteristics of glycosylated proteins and solving their three-dimensional structures requires homogeneous recombinant protein of high quality.We introduce here a new approach to produce glycoproteins in homogenous form with the well-established, glycosylation mutant CHO Lec3.2.8.1 cells. Using preparative cell sorting, stable, high-expressing GFP ‘master’ cell lines were generated that can be converted fast and reliably by targeted integration via Flp recombinase-mediated cassette exchange (RMCE) to produce any glycoprotein. Small-scale transient transfection of HEK293 cells was used to identify genetically engineered constructs suitable for constructing stable cell lines. Stable cell lines expressing 10 different proteins were established. The system was validated by expression, purification, deglycosylation and crystallization of the heavily glycosylated luminal domains of lysosome-associated membrane proteins (LAMP). |
format | Online Article Text |
id | pubmed-3235087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32350872011-12-15 Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development Wilke, Sonja Groebe, Lothar Maffenbeier, Vitali Jäger, Volker Gossen, Manfred Josewski, Jörn Duda, Agathe Polle, Lilia Owens, Raymond J. Wirth, Dagmar Heinz, Dirk W. van den Heuvel, Joop Büssow, Konrad PLoS One Research Article Studying the biophysical characteristics of glycosylated proteins and solving their three-dimensional structures requires homogeneous recombinant protein of high quality.We introduce here a new approach to produce glycoproteins in homogenous form with the well-established, glycosylation mutant CHO Lec3.2.8.1 cells. Using preparative cell sorting, stable, high-expressing GFP ‘master’ cell lines were generated that can be converted fast and reliably by targeted integration via Flp recombinase-mediated cassette exchange (RMCE) to produce any glycoprotein. Small-scale transient transfection of HEK293 cells was used to identify genetically engineered constructs suitable for constructing stable cell lines. Stable cell lines expressing 10 different proteins were established. The system was validated by expression, purification, deglycosylation and crystallization of the heavily glycosylated luminal domains of lysosome-associated membrane proteins (LAMP). Public Library of Science 2011-12-09 /pmc/articles/PMC3235087/ /pubmed/22174749 http://dx.doi.org/10.1371/journal.pone.0027829 Text en Wilke et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wilke, Sonja Groebe, Lothar Maffenbeier, Vitali Jäger, Volker Gossen, Manfred Josewski, Jörn Duda, Agathe Polle, Lilia Owens, Raymond J. Wirth, Dagmar Heinz, Dirk W. van den Heuvel, Joop Büssow, Konrad Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development |
title | Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development |
title_full | Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development |
title_fullStr | Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development |
title_full_unstemmed | Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development |
title_short | Streamlining Homogeneous Glycoprotein Production for Biophysical and Structural Applications by Targeted Cell Line Development |
title_sort | streamlining homogeneous glycoprotein production for biophysical and structural applications by targeted cell line development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235087/ https://www.ncbi.nlm.nih.gov/pubmed/22174749 http://dx.doi.org/10.1371/journal.pone.0027829 |
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