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Journal Article

Phase separation in the isolation and purification of membrane proteins

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Arnold,  T
Department Protein Evolution, Max Planck Institute for Developmental Biology, Max Planck Society;

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Linke,  D
Department Protein Evolution, Max Planck Institute for Developmental Biology, Max Planck Society;

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Citation

Arnold, T., & Linke, D. (2007). Phase separation in the isolation and purification of membrane proteins. Biotechniques, 43(4), 427-430. doi:10.2144/000112566.


Cite as: https://hdl.handle.net/21.11116/0000-000A-F2F0-5
Abstract
Phase separation is a simple, efficient, and cheap method to purify and concentrate detergent-solubilized membrane proteins. In spite of this, phase separation is not widely used or even known among membrane protein scientists, and ready-to-use protocols are available for only relatively few detergent/membrane protein combinations. Here, we summarize the physical and chemical parameters that influence the phase separation behavior of detergents commonly used for membrane protein studies. Examples for the successful purification of membrane proteins using this method with different classes of detergents are provided. As the choice of the detergent is critical in many downstream applications (e.g., membrane protein crystallization or functional assays), we discuss how new phase separation protocols can be developed for a given detergent buffer system.