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Heterologous Expression of Membrane Proteins

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Cover of 'Heterologous Expression of Membrane Proteins'

Table of Contents

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    Book Overview
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    Chapter 1 Heterologous Expression of Membrane Proteins
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    Chapter 2 Heterologous Expression of Membrane Proteins
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    Chapter 3 Membrane Protein Production in Escherichia coli: Protocols and Rules.
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    Chapter 4 Codon Optimizing for Increased Membrane Protein Production: A Minimalist Approach.
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    Chapter 5 Generation of Tetracycline-Inducible Mammalian Cell Lines by Flow Cytometry for Improved Overproduction of Membrane Proteins.
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    Chapter 6 Membrane Protein Production in Lactococcus lactis for Functional Studies.
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    Chapter 7 Heterologous Expression of Membrane Proteins
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    Chapter 8 Leishmania tarentolae as a Promising Tool for Expressing Polytopic and Multi-Transmembrane Spans Eukaryotic Membrane Proteins: The Case of the ABC Pump ABCG6.
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    Chapter 9 Overexpression, Membrane Preparation, and Purification of a Typical Multidrug ABC Transporter BmrA.
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    Chapter 10 Heterologous Expression of Membrane Proteins
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    Chapter 11 Heterologous Expression of Membrane Proteins
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    Chapter 12 Heterologous Expression of Membrane Proteins
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    Chapter 13 Heterologous Expression of Membrane Proteins
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    Chapter 14 Heterologous Expression of Membrane Proteins
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    Chapter 15 Membrane Protein Solubilization and Composition of Protein Detergent Complexes.
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    Chapter 16 Detergent-Free Membrane Protein Purification.
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    Chapter 17 Conformational Dynamics and Interactions of Membrane Proteins by Hydrogen/Deuterium Mass Spectrometry.
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    Chapter 18 Lessons from an α-Helical Membrane Enzyme: Expression, Purification, and Detergent Optimization for Biophysical and Structural Characterization.
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    Chapter 19 Heterologous Expression of Membrane Proteins
Attention for Chapter 15: Membrane Protein Solubilization and Composition of Protein Detergent Complexes.
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Chapter title
Membrane Protein Solubilization and Composition of Protein Detergent Complexes.
Chapter number 15
Book title
Heterologous Expression of Membrane Proteins
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3637-3_15
Pubmed ID
Book ISBNs
978-1-4939-3635-9, 978-1-4939-3637-3
Authors

Katia Duquesne, Valérie Prima, James N. Sturgis

Editors

Isabelle Mus-Veteau

Abstract

Membrane proteins are typically expressed in heterologous systems with a view to in vitro characterization. A critical step in the preparation of membrane proteins after expression in any system is the solubilization of the protein in aqueous solution, typically using detergents and lipids, to obtain the protein in a form suitable for purification, structural or functional analysis. This process is particularly difficult as the objective is to prepare the protein in an unnatural environment, a protein detergent complex, separating it from its natural lipid partners while causing the minimum destabilization or modification of the structure. Although the process is difficult, and relatively hard to master, an increasing number of membrane proteins have been successfully isolated after expression in a wide variety of systems. In this chapter we give a general protocol for preparing protein detergent complexes that is aimed at guiding the reader through the different critical steps. In the second part of the chapter we illustrate how to analyze the composition of protein detergent complexes; this analysis is important as it has been found that compositional variation often causes irreproducible results.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 24%
Student > Bachelor 3 18%
Researcher 3 18%
Professor > Associate Professor 2 12%
Student > Master 2 12%
Other 1 6%
Unknown 2 12%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 41%
Agricultural and Biological Sciences 3 18%
Pharmacology, Toxicology and Pharmaceutical Science 1 6%
Social Sciences 1 6%
Neuroscience 1 6%
Other 0 0%
Unknown 4 24%