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Revolutionizing membrane protein overexpression in bacteria

The bacterium Escherichia coli is the most widely used expression host for overexpression trials of membrane proteins. Usually, different strains, culture conditions and expression regimes are screened for to identify the optimal overexpression strategy. However, yields are often not satisfactory, e...

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Detalles Bibliográficos
Autores principales: Schlegel, Susan, Klepsch, Mirjam, Gialama, Dimitra, Wickström, David, Slotboom, Dirk Jan, De Gier, Jan‐Willem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815807/
https://www.ncbi.nlm.nih.gov/pubmed/21255339
http://dx.doi.org/10.1111/j.1751-7915.2009.00148.x
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author Schlegel, Susan
Klepsch, Mirjam
Gialama, Dimitra
Wickström, David
Slotboom, Dirk Jan
De Gier, Jan‐Willem
author_facet Schlegel, Susan
Klepsch, Mirjam
Gialama, Dimitra
Wickström, David
Slotboom, Dirk Jan
De Gier, Jan‐Willem
author_sort Schlegel, Susan
collection PubMed
description The bacterium Escherichia coli is the most widely used expression host for overexpression trials of membrane proteins. Usually, different strains, culture conditions and expression regimes are screened for to identify the optimal overexpression strategy. However, yields are often not satisfactory, especially for eukaryotic membrane proteins. This has initiated a revolution of membrane protein overexpression in bacteria. Recent studies have shown that it is feasible to (i) engineer or select for E. coli strains with strongly improved membrane protein overexpression characteristics, (ii) use bacteria other than E. coli for the expression of membrane proteins, (iii) engineer or select for membrane protein variants that retain functionality but express better than the wild‐type protein, and (iv) express membrane proteins using E. coli‐based cell‐free systems.
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spelling pubmed-38158072014-02-12 Revolutionizing membrane protein overexpression in bacteria Schlegel, Susan Klepsch, Mirjam Gialama, Dimitra Wickström, David Slotboom, Dirk Jan De Gier, Jan‐Willem Microb Biotechnol Minireviews The bacterium Escherichia coli is the most widely used expression host for overexpression trials of membrane proteins. Usually, different strains, culture conditions and expression regimes are screened for to identify the optimal overexpression strategy. However, yields are often not satisfactory, especially for eukaryotic membrane proteins. This has initiated a revolution of membrane protein overexpression in bacteria. Recent studies have shown that it is feasible to (i) engineer or select for E. coli strains with strongly improved membrane protein overexpression characteristics, (ii) use bacteria other than E. coli for the expression of membrane proteins, (iii) engineer or select for membrane protein variants that retain functionality but express better than the wild‐type protein, and (iv) express membrane proteins using E. coli‐based cell‐free systems. Blackwell Publishing Ltd 2010-07 2010-06-24 /pmc/articles/PMC3815807/ /pubmed/21255339 http://dx.doi.org/10.1111/j.1751-7915.2009.00148.x Text en Copyright © 2009 The Authors. Journal compilation © 2009 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Minireviews
Schlegel, Susan
Klepsch, Mirjam
Gialama, Dimitra
Wickström, David
Slotboom, Dirk Jan
De Gier, Jan‐Willem
Revolutionizing membrane protein overexpression in bacteria
title Revolutionizing membrane protein overexpression in bacteria
title_full Revolutionizing membrane protein overexpression in bacteria
title_fullStr Revolutionizing membrane protein overexpression in bacteria
title_full_unstemmed Revolutionizing membrane protein overexpression in bacteria
title_short Revolutionizing membrane protein overexpression in bacteria
title_sort revolutionizing membrane protein overexpression in bacteria
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815807/
https://www.ncbi.nlm.nih.gov/pubmed/21255339
http://dx.doi.org/10.1111/j.1751-7915.2009.00148.x
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