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Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG
Human ether-a-gogo related gene (hERG) product is the membrane potassium channel Kv11.1, which is involved in the electrical activity of the heart. As such, it is a key player in the toxicity of many drug candidates. Therefore, having this protein at hand during earlier stages of drug discovery is i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651182/ https://www.ncbi.nlm.nih.gov/pubmed/31261773 http://dx.doi.org/10.3390/ijms20133181 |
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author | Vasseur, Lucie Cens, Thierry Wagner, Renaud Saint, Nathalie Kugler, Valérie Chavanieu, Alain Ouvry, Christine Dupré, Clémence Ferry, Gilles Boutin, Jean A. |
author_facet | Vasseur, Lucie Cens, Thierry Wagner, Renaud Saint, Nathalie Kugler, Valérie Chavanieu, Alain Ouvry, Christine Dupré, Clémence Ferry, Gilles Boutin, Jean A. |
author_sort | Vasseur, Lucie |
collection | PubMed |
description | Human ether-a-gogo related gene (hERG) product is the membrane potassium channel Kv11.1, which is involved in the electrical activity of the heart. As such, it is a key player in the toxicity of many drug candidates. Therefore, having this protein at hand during earlier stages of drug discovery is important for preventing later toxicity. Furthermore, having a fair quantity of functional channels may help in the development of the necessary techniques for gaining insight in this channel structure. Thus, we performed a comparative study of methods for over-expressing a mutated but functional, hERG in different orthologous hosts, such as yeast, bacteria, insect and human cell lines. We also engineered the protein to test various constructs of a functional channel. We obtained a significant amount of a functional mutant channel from HEK cells that we thoroughly characterized. The present work paves the way for the expression of large amounts of this protein, with which protein crystallization or cryo-electronic microscopy will be attempted. This will be a way to gain information on the structure of the hERG active site and its modelization to obtain data on the pauses of various reference compounds from the pharmacopeia, as well as to gain information about the thermodynamics of the hERG/ligand relationship. |
format | Online Article Text |
id | pubmed-6651182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66511822019-08-07 Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG Vasseur, Lucie Cens, Thierry Wagner, Renaud Saint, Nathalie Kugler, Valérie Chavanieu, Alain Ouvry, Christine Dupré, Clémence Ferry, Gilles Boutin, Jean A. Int J Mol Sci Article Human ether-a-gogo related gene (hERG) product is the membrane potassium channel Kv11.1, which is involved in the electrical activity of the heart. As such, it is a key player in the toxicity of many drug candidates. Therefore, having this protein at hand during earlier stages of drug discovery is important for preventing later toxicity. Furthermore, having a fair quantity of functional channels may help in the development of the necessary techniques for gaining insight in this channel structure. Thus, we performed a comparative study of methods for over-expressing a mutated but functional, hERG in different orthologous hosts, such as yeast, bacteria, insect and human cell lines. We also engineered the protein to test various constructs of a functional channel. We obtained a significant amount of a functional mutant channel from HEK cells that we thoroughly characterized. The present work paves the way for the expression of large amounts of this protein, with which protein crystallization or cryo-electronic microscopy will be attempted. This will be a way to gain information on the structure of the hERG active site and its modelization to obtain data on the pauses of various reference compounds from the pharmacopeia, as well as to gain information about the thermodynamics of the hERG/ligand relationship. MDPI 2019-06-28 /pmc/articles/PMC6651182/ /pubmed/31261773 http://dx.doi.org/10.3390/ijms20133181 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vasseur, Lucie Cens, Thierry Wagner, Renaud Saint, Nathalie Kugler, Valérie Chavanieu, Alain Ouvry, Christine Dupré, Clémence Ferry, Gilles Boutin, Jean A. Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG |
title | Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG |
title_full | Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG |
title_fullStr | Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG |
title_full_unstemmed | Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG |
title_short | Importance of the Choice of a Recombinant System to Produce Large Amounts of Functional Membrane Protein hERG |
title_sort | importance of the choice of a recombinant system to produce large amounts of functional membrane protein herg |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6651182/ https://www.ncbi.nlm.nih.gov/pubmed/31261773 http://dx.doi.org/10.3390/ijms20133181 |
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