Synthetic Biology-Based Solution NMR Studies on Membrane Proteins in Lipid Environments.


Journal

Methods in enzymology
ISSN: 1557-7988
Titre abrégé: Methods Enzymol
Pays: United States
ID NLM: 0212271

Informations de publication

Date de publication:
2019
Historique:
entrez: 7 1 2019
pubmed: 7 1 2019
medline: 20 8 2019
Statut: ppublish

Résumé

Although membrane proteins are in the focus of biochemical research for many decades the general knowledge of this important class is far behind soluble proteins. Despite several recent technical developments, the most challenging feature still is the generation of high-quality samples in environments suitable for the selected application. Reconstitution of membrane proteins into lipid bilayers will generate the most native-like environment and is therefore commonly desired. However, it poses tremendous problems to solution-state NMR analysis due to the dramatic increase in particle size resulting in high rotational correlation times. Nevertheless, a few promising strategies for the solution NMR analysis of membrane inserted proteins are emerging and will be discussed in this chapter. We focus on the generation of membrane protein samples in nanodisc membranes by cell-free systems and will describe the characteristic advantages of that platform in providing tailored protein expression and folding environments. We indicate frequent problems that have to be overcome in cell-free synthesis, nanodisc preparation, and customization for samples dedicated for solution-state NMR. Detailed instructions for sample preparation are given, and solution NMR approaches suitable for membrane proteins in bilayers are compiled. We further discuss the current strategies applied for signal detection from such difficult samples and describe the type of information that can be extracted from the various experiments. In summary, a comprehensive guideline for the analysis of membrane proteins in native-like membrane environments by solution-state NMR techniques will be provided.

Identifiants

pubmed: 30611423
pii: S0076-6879(18)30297-0
doi: 10.1016/bs.mie.2018.08.019
pii:
doi:

Substances chimiques

Lipid Bilayers 0
Membrane Proteins 0
Viral Proteins 0
Phosphorylcholine 107-73-3
dodecylphosphocholine 53949-18-1
bacteriophage T7 RNA polymerase EC 2.7.7.-
DNA-Directed RNA Polymerases EC 2.7.7.6
Sodium Cholate NU3Y4CCH8Z

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

143-185

Informations de copyright

© 2019 Elsevier Inc. All rights reserved.

Auteurs

Erik Henrich (E)

Institute of Biophysical Chemistry, Centre for Biomolecular Magnetic Resonance, J.W. Goethe-University, Frankfurt am Main, Germany.

Frank Löhr (F)

Institute of Biophysical Chemistry, Centre for Biomolecular Magnetic Resonance, J.W. Goethe-University, Frankfurt am Main, Germany.

Julija Mezhyrova (J)

Institute of Biophysical Chemistry, Centre for Biomolecular Magnetic Resonance, J.W. Goethe-University, Frankfurt am Main, Germany.

Aisha Laguerre (A)

Institute of Biophysical Chemistry, Centre for Biomolecular Magnetic Resonance, J.W. Goethe-University, Frankfurt am Main, Germany.

Frank Bernhard (F)

Institute of Biophysical Chemistry, Centre for Biomolecular Magnetic Resonance, J.W. Goethe-University, Frankfurt am Main, Germany.

Volker Dötsch (V)

Institute of Biophysical Chemistry, Centre for Biomolecular Magnetic Resonance, J.W. Goethe-University, Frankfurt am Main, Germany. Electronic address: vdoetsch@em.uni-frankfurt.de.

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Classifications MeSH