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The Penn State Protein Ladder system for inexpensive protein molecular weight markers
We have created the Penn State Protein Ladder system to produce protein molecular weight markers easily and inexpensively (less than a penny a lane). The system includes plasmids which express 10, 15, 20, 30, 40, 50, 60, 80 and 100 kD proteins in E. coli. Each protein migrates appropriately on SDS-P...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373980/ https://www.ncbi.nlm.nih.gov/pubmed/34408191 http://dx.doi.org/10.1038/s41598-021-96051-x |
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author | Santilli, Ryan T. Williamson, John E. Shibata, Yoshitaka Sowers, Rosalie P. Fleischman, Andrew N. Tan, Song |
author_facet | Santilli, Ryan T. Williamson, John E. Shibata, Yoshitaka Sowers, Rosalie P. Fleischman, Andrew N. Tan, Song |
author_sort | Santilli, Ryan T. |
collection | PubMed |
description | We have created the Penn State Protein Ladder system to produce protein molecular weight markers easily and inexpensively (less than a penny a lane). The system includes plasmids which express 10, 15, 20, 30, 40, 50, 60, 80 and 100 kD proteins in E. coli. Each protein migrates appropriately on SDS-PAGE gels, is expressed at very high levels (10–50 mg per liter of culture), is easy to purify via histidine tags and can be detected directly on Western blots via engineered immunoglobulin binding domains. We have also constructed plasmids to express 150 and 250 kD proteins. For more efficient production, we have created two polycistronic expression vectors which coexpress the 10, 30, 50, 100 kD proteins or the 20, 40, 60, 80 kD proteins. 50 ml of culture is sufficient to produce 20,000 lanes of individual ladder protein or 3750 lanes of each set of coexpressed ladder proteins. These Penn State Protein Ladder expression plasmids also constitute useful reagents for teaching laboratories to demonstrate recombinant expression in E. coli and affinity protein purification, and to research laboratories desiring positive controls for recombinant protein expression and purification. |
format | Online Article Text |
id | pubmed-8373980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83739802021-08-20 The Penn State Protein Ladder system for inexpensive protein molecular weight markers Santilli, Ryan T. Williamson, John E. Shibata, Yoshitaka Sowers, Rosalie P. Fleischman, Andrew N. Tan, Song Sci Rep Article We have created the Penn State Protein Ladder system to produce protein molecular weight markers easily and inexpensively (less than a penny a lane). The system includes plasmids which express 10, 15, 20, 30, 40, 50, 60, 80 and 100 kD proteins in E. coli. Each protein migrates appropriately on SDS-PAGE gels, is expressed at very high levels (10–50 mg per liter of culture), is easy to purify via histidine tags and can be detected directly on Western blots via engineered immunoglobulin binding domains. We have also constructed plasmids to express 150 and 250 kD proteins. For more efficient production, we have created two polycistronic expression vectors which coexpress the 10, 30, 50, 100 kD proteins or the 20, 40, 60, 80 kD proteins. 50 ml of culture is sufficient to produce 20,000 lanes of individual ladder protein or 3750 lanes of each set of coexpressed ladder proteins. These Penn State Protein Ladder expression plasmids also constitute useful reagents for teaching laboratories to demonstrate recombinant expression in E. coli and affinity protein purification, and to research laboratories desiring positive controls for recombinant protein expression and purification. Nature Publishing Group UK 2021-08-18 /pmc/articles/PMC8373980/ /pubmed/34408191 http://dx.doi.org/10.1038/s41598-021-96051-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Santilli, Ryan T. Williamson, John E. Shibata, Yoshitaka Sowers, Rosalie P. Fleischman, Andrew N. Tan, Song The Penn State Protein Ladder system for inexpensive protein molecular weight markers |
title | The Penn State Protein Ladder system for inexpensive protein molecular weight markers |
title_full | The Penn State Protein Ladder system for inexpensive protein molecular weight markers |
title_fullStr | The Penn State Protein Ladder system for inexpensive protein molecular weight markers |
title_full_unstemmed | The Penn State Protein Ladder system for inexpensive protein molecular weight markers |
title_short | The Penn State Protein Ladder system for inexpensive protein molecular weight markers |
title_sort | penn state protein ladder system for inexpensive protein molecular weight markers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373980/ https://www.ncbi.nlm.nih.gov/pubmed/34408191 http://dx.doi.org/10.1038/s41598-021-96051-x |
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