Perturbations of Native Membrane Protein Structure in Alkyl Phosphocholine Detergents: A Critical Assessment of NMR and Biophysical Studies.
Schnell, Jason R
Catoire, Laurent J
Cross, Timothy A
American Chemical Society (ACS)
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Chipot, C., Dehez, F., Schnell, J. R., Zitzmann, N., Pebay-Peyroula, E., Catoire, L. J., Miroux, B., et al. (2018). Perturbations of Native Membrane Protein Structure in Alkyl Phosphocholine Detergents: A Critical Assessment of NMR and Biophysical Studies.. Chem Rev, 118 (7), 3559-3607. https://doi.org/10.1021/acs.chemrev.7b00570
Membrane proteins perform a host of vital cellular functions. Deciphering the molecular mechanisms whereby they fulfill these functions requires detailed biophysical and structural investigations. Detergents have proven pivotal to extract the protein from its native surroundings. Yet, they provide a milieu that departs significantly from that of the biological membrane, to the extent that the structure, the dynamics, and the interactions of membrane proteins in detergents may considerably vary, as compared to the native environment. Understanding the impact of detergents on membrane proteins is, therefore, crucial to assess the biological relevance of results obtained in detergents. Here, we review the strengths and weaknesses of alkyl phosphocholines (or foscholines), the most widely used detergent in solution-NMR studies of membrane proteins. While this class of detergents is often successful for membrane protein solubilization, a growing list of examples points to destabilizing and denaturing properties, in particular for α-helical membrane proteins. Our comprehensive analysis stresses the importance of stringent controls when working with this class of detergents and when analyzing the structure and dynamics of membrane proteins in alkyl phosphocholine detergents.
Cell Membrane, Animals, Humans, Phosphorylcholine, Membrane Proteins, Detergents, Magnetic Resonance Spectroscopy, Protein Conformation, Protein Folding, Kinetics, Micelles, Solubility, Models, Molecular, Protein Stability, Biophysical Phenomena, Hydrophobic and Hydrophilic Interactions
Medical Research Council (MC_U105663139)
Biotechnology and Biological Sciences Research Council (BB/R50564X/1)
Medical Research Council (MC_UU_00015/1)
External DOI: https://doi.org/10.1021/acs.chemrev.7b00570
This record's URL: https://www.repository.cam.ac.uk/handle/1810/275103