UMMS Affiliation
Department of Biochemistry and Molecular Pharmacology; Graduate School of Biomedical Sciences
Publication Date
2018-12-17
Document Type
Article
Disciplines
Amino Acids, Peptides, and Proteins | Biochemistry | Biophysics | Lipids | Molecular Biology | Structural Biology
Abstract
The use of styrene-maleic acid (SMA) for the purification of a wide range of membrane proteins (MPs) from both prokaryotic and eukaryotic sources has begun to make an impact in the field of MP biology. This method is growing in popularity as a means to purify and thoroughly investigate the structure and function of MPs and biological membranes. The amphiphilic SMA copolymer can effectively extract MPs directly from a native lipid bilayer to form discs approximately 10 nm in diameter. The resulting lipid particles, or styrene-maleic acid lipid particles (SMALPs), contain SMA, protein and membrane lipid. MPs purified in SMALPs are able to retain their native structure and, in many cases, functional activity, and growing evidence suggests that MPs purified using SMA have enhanced thermal stability compared with detergent-purified proteins. The SMALP method is versatile and is compatible with a wide range of cell types across taxonomic domains. It can readily be adapted to replace detergent in many protein purification methods, often with only minor changes made to the existing protocol. Moreover, biophysical analysis and structural determination may now be a possibility for many large, unstable MPs. Here, we review recent advances in the area of SMALP purification and how it is affecting the field of MP biology, critically assess recent progress made with this method, address some of the associated technical challenges which may remain unresolved and discuss opportunities for exploiting SMALPs to expand our understanding of structural and functional properties of MPs.
Keywords
membrane proteins, protein purification, structural biology, structural characterisation
Rights and Permissions
© 2018 The Author(s). This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND).
DOI of Published Version
10.1042/BST20180139
Source
Biochem Soc Trans. 2018 Dec 17;46(6):1495-1504. doi: 10.1042/BST20180139. Epub 2018 Nov 21. Link to article on publisher's site
Journal/Book/Conference Title
Biochemical Society transactions
Related Resources
PubMed ID
30464048
Repository Citation
Simon, Kailene S.; Pollock, Naomi L.; and Lee, Sarah C., "Membrane protein nanoparticles: the shape of things to come" (2018). Open Access Articles. 3696.
https://escholarship.umassmed.edu/oapubs/3696
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Included in
Amino Acids, Peptides, and Proteins Commons, Biochemistry Commons, Biophysics Commons, Lipids Commons, Molecular Biology Commons, Structural Biology Commons