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A simple procedure for bacterial expression and purification of the fragile X protein family
The fragile X protein family consists of three RNA-binding proteins involved in translational regulation. Fragile X mental retardation protein (FMRP) is well-studied, as its loss leads to fragile X syndrome, a neurodevelopmental disorder which is the most prevalent form of inherited mental retardati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522082/ https://www.ncbi.nlm.nih.gov/pubmed/32985615 http://dx.doi.org/10.1038/s41598-020-72984-7 |
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author | Edwards, Madison Xu, Mingzhi Joseph, Simpson |
author_facet | Edwards, Madison Xu, Mingzhi Joseph, Simpson |
author_sort | Edwards, Madison |
collection | PubMed |
description | The fragile X protein family consists of three RNA-binding proteins involved in translational regulation. Fragile X mental retardation protein (FMRP) is well-studied, as its loss leads to fragile X syndrome, a neurodevelopmental disorder which is the most prevalent form of inherited mental retardation and the primary monogenetic cause of autism. Fragile X related proteins 1 and 2 (FXR1P and FXR2P) are autosomal paralogs of FMRP that are involved in promoting muscle development and neural development, respectively. There is great interest in studying this family of proteins, yet researchers have faced much difficulty in expressing and purifying the full-length versions of these proteins in sufficient quantities. We have developed a simple, rapid, and inexpensive procedure that allows for the recombinant expression and purification of full-length human FMRP, FXR1P, and FXR2P from Escherichia coli in high yields, free of protein and nucleic acid contamination. In order to assess the proteins’ function after purification, we confirmed their binding to pseudoknot and G-quadruplex forming RNAs as well as their ability to regulate translation in vitro. |
format | Online Article Text |
id | pubmed-7522082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75220822020-09-29 A simple procedure for bacterial expression and purification of the fragile X protein family Edwards, Madison Xu, Mingzhi Joseph, Simpson Sci Rep Article The fragile X protein family consists of three RNA-binding proteins involved in translational regulation. Fragile X mental retardation protein (FMRP) is well-studied, as its loss leads to fragile X syndrome, a neurodevelopmental disorder which is the most prevalent form of inherited mental retardation and the primary monogenetic cause of autism. Fragile X related proteins 1 and 2 (FXR1P and FXR2P) are autosomal paralogs of FMRP that are involved in promoting muscle development and neural development, respectively. There is great interest in studying this family of proteins, yet researchers have faced much difficulty in expressing and purifying the full-length versions of these proteins in sufficient quantities. We have developed a simple, rapid, and inexpensive procedure that allows for the recombinant expression and purification of full-length human FMRP, FXR1P, and FXR2P from Escherichia coli in high yields, free of protein and nucleic acid contamination. In order to assess the proteins’ function after purification, we confirmed their binding to pseudoknot and G-quadruplex forming RNAs as well as their ability to regulate translation in vitro. Nature Publishing Group UK 2020-09-28 /pmc/articles/PMC7522082/ /pubmed/32985615 http://dx.doi.org/10.1038/s41598-020-72984-7 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Edwards, Madison Xu, Mingzhi Joseph, Simpson A simple procedure for bacterial expression and purification of the fragile X protein family |
title | A simple procedure for bacterial expression and purification of the fragile X protein family |
title_full | A simple procedure for bacterial expression and purification of the fragile X protein family |
title_fullStr | A simple procedure for bacterial expression and purification of the fragile X protein family |
title_full_unstemmed | A simple procedure for bacterial expression and purification of the fragile X protein family |
title_short | A simple procedure for bacterial expression and purification of the fragile X protein family |
title_sort | simple procedure for bacterial expression and purification of the fragile x protein family |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522082/ https://www.ncbi.nlm.nih.gov/pubmed/32985615 http://dx.doi.org/10.1038/s41598-020-72984-7 |
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