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Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature
BACKGROUND: HERG potassium channel blockade is the major cause for drug-induced long QT syndrome, which sometimes cause cardiac disrhythmias and sudden death. There is a strong interest in the pharmaceutical industry to develop high quality medium to high-throughput assays for detecting compounds wi...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241608/ https://www.ncbi.nlm.nih.gov/pubmed/18096051 http://dx.doi.org/10.1186/1472-6750-7-93 |
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author | Chen, Mao Xiang Sandow, Shaun L Doceul, Virginie Chen, Yu Hua Harper, Heather Hamilton, Bruce Meadows, Helen J Trezise, Derek J Clare, Jeff J |
author_facet | Chen, Mao Xiang Sandow, Shaun L Doceul, Virginie Chen, Yu Hua Harper, Heather Hamilton, Bruce Meadows, Helen J Trezise, Derek J Clare, Jeff J |
author_sort | Chen, Mao Xiang |
collection | PubMed |
description | BACKGROUND: HERG potassium channel blockade is the major cause for drug-induced long QT syndrome, which sometimes cause cardiac disrhythmias and sudden death. There is a strong interest in the pharmaceutical industry to develop high quality medium to high-throughput assays for detecting compounds with potential cardiac liability at the earliest stages of drug development. Cultivation of cells at lower temperature has been used to improve the folding and membrane localization of trafficking defective hERG mutant proteins. The objective of this study was to investigate the effect of lower temperature maintenance on wild type hERG expression and assay performance. RESULTS: Wild type hERG was stably expressed in CHO-K1 cells, with the majority of channel protein being located in the cytoplasm, but relatively little on the cell surface. Expression at both locations was increased several-fold by cultivation at lower growth temperatures. Intracellular hERG protein levels were highest at 27°C and this correlated with maximal (3)H-dofetilide binding activity. In contrast, the expression of functionally active cell surface-associated hERG measured by patch clamp electrophysiology was optimal at 30°C. The majority of the cytoplasmic hERG protein was associated with the membranes of cytoplasmic vesicles, which markedly increased in quantity and size at lower temperatures or in the presence of the Ca(2+)-ATPase inhibitor, thapsigargin. Incubation with the endocytic trafficking blocker, nocodazole, led to an increase in hERG activity at 37°C, but not at 30°C. CONCLUSION: Our results are consistent with the concept that maintenance of cells at reduced temperature can be used to boost the functional expression of difficult-to-express membrane proteins and improve the quality of assays for medium to high-throughput compound screening. In addition, these results shed some light on the trafficking of hERG protein under these growth conditions. |
format | Text |
id | pubmed-2241608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22416082008-02-13 Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature Chen, Mao Xiang Sandow, Shaun L Doceul, Virginie Chen, Yu Hua Harper, Heather Hamilton, Bruce Meadows, Helen J Trezise, Derek J Clare, Jeff J BMC Biotechnol Research Article BACKGROUND: HERG potassium channel blockade is the major cause for drug-induced long QT syndrome, which sometimes cause cardiac disrhythmias and sudden death. There is a strong interest in the pharmaceutical industry to develop high quality medium to high-throughput assays for detecting compounds with potential cardiac liability at the earliest stages of drug development. Cultivation of cells at lower temperature has been used to improve the folding and membrane localization of trafficking defective hERG mutant proteins. The objective of this study was to investigate the effect of lower temperature maintenance on wild type hERG expression and assay performance. RESULTS: Wild type hERG was stably expressed in CHO-K1 cells, with the majority of channel protein being located in the cytoplasm, but relatively little on the cell surface. Expression at both locations was increased several-fold by cultivation at lower growth temperatures. Intracellular hERG protein levels were highest at 27°C and this correlated with maximal (3)H-dofetilide binding activity. In contrast, the expression of functionally active cell surface-associated hERG measured by patch clamp electrophysiology was optimal at 30°C. The majority of the cytoplasmic hERG protein was associated with the membranes of cytoplasmic vesicles, which markedly increased in quantity and size at lower temperatures or in the presence of the Ca(2+)-ATPase inhibitor, thapsigargin. Incubation with the endocytic trafficking blocker, nocodazole, led to an increase in hERG activity at 37°C, but not at 30°C. CONCLUSION: Our results are consistent with the concept that maintenance of cells at reduced temperature can be used to boost the functional expression of difficult-to-express membrane proteins and improve the quality of assays for medium to high-throughput compound screening. In addition, these results shed some light on the trafficking of hERG protein under these growth conditions. BioMed Central 2007-12-20 /pmc/articles/PMC2241608/ /pubmed/18096051 http://dx.doi.org/10.1186/1472-6750-7-93 Text en Copyright © 2007 Chen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Mao Xiang Sandow, Shaun L Doceul, Virginie Chen, Yu Hua Harper, Heather Hamilton, Bruce Meadows, Helen J Trezise, Derek J Clare, Jeff J Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature |
title | Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature |
title_full | Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature |
title_fullStr | Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature |
title_full_unstemmed | Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature |
title_short | Improved functional expression of recombinant human ether-a-go-go (hERG) K(+ )channels by cultivation at reduced temperature |
title_sort | improved functional expression of recombinant human ether-a-go-go (herg) k(+ )channels by cultivation at reduced temperature |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241608/ https://www.ncbi.nlm.nih.gov/pubmed/18096051 http://dx.doi.org/10.1186/1472-6750-7-93 |
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