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Selective extraction systems for detection and purification of membrane proteins

Sivars, Ulf LU (2000)
Abstract
Increased understanding of membrane proteins is important for characterization of biochemical processes. Improved membrane protein isolation methods is a key issue for effective functional and structural determination of the large amount of unknown membrane proteins.



In this thesis, a novel approach towards selective membrane protein purification is introduced. Polymer induced micelle extraction (PIME) systems are formed in mixtures between nonionic detergents and water-soluble polymers. Over a critical concentration the detergent/polymer/water mixture separates into two phases and forms a detergent-rich and a polymer-rich phase. Separation of membrane proteins from cytosolic proteins and insoluble materials is achieved... (More)
Increased understanding of membrane proteins is important for characterization of biochemical processes. Improved membrane protein isolation methods is a key issue for effective functional and structural determination of the large amount of unknown membrane proteins.



In this thesis, a novel approach towards selective membrane protein purification is introduced. Polymer induced micelle extraction (PIME) systems are formed in mixtures between nonionic detergents and water-soluble polymers. Over a critical concentration the detergent/polymer/water mixture separates into two phases and forms a detergent-rich and a polymer-rich phase. Separation of membrane proteins from cytosolic proteins and insoluble materials is achieved by the large difference in distribution between the phases. In general, membrane proteins are extracted into the micelle-enriched phase, while water-soluble proteins partitions in the polymer-rich phase. Membranes can be solubilized directly into the PIME system at low temperature with many commonly used nonionic detergents. The developed micelle-based extraction system is suggested to replace the traditional solubilization step in membrane protein purification. A combined solubilization and primary purification of the target proteins can be obtained. Such smart solubilization in PIME systems was utilized to pre-fractionate membrane proteins prior to detection of a putative membrane bound receptor.



The partitioning and phase separation mechanism in the PIME systems was examined in detail and explained in a thermodynamic context. An understanding how to optimize the system for membrane protein extraction was gained. Several approaches to further increase the separation between hydrophobic and hydrophilic proteins was studied such as addition of affinity ligands, salts and ionic detergents. A novel high-resolution method was developed, called affinity PIME systems. A selective membrane protein extraction system was obtained by affinity partitioning of the target membrane protein into the polymer-rich phase, while contaminating membrane proteins remained in the opposite micelle-rich phase. The concept was successfully demonstrated by metal affinity purification of the His-tagged integral membrane protein, cytochrome bo3 ubiquinol oxidase from Escherichia coli membranes. Affinity PIME systems should be of great importance for a fast purification of structural intact membrane proteins due the mild and selective properties of the system.



PIME systems can be applied for purification of amphiphilic fusion proteins. An effective purification of the amphiphilic fusion protein endoglucanase I-hydrophobin I was obtained from a Trichoderma reesei fermentation filtrate. A method was developed for removal of detergent from the purified fusion protein. (Less)
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author
supervisor
opponent
  • Professor Lundahl, Per, Department of Biochemistry, Uppsala University, Sweden
organization
publishing date
type
Thesis
publication status
published
subject
keywords
partitioning, Aqueous two-phase systems, separation, membrane proteins, detergent, micelle, polymer, Biochemistry, affinity, Metabolism, Biokemi
pages
116 pages
publisher
Ulf Sivars, Department of Biochemistry, Center for Chemistry and Chemical Engineering, Lund University
defense location
Lecture Hall C, Chemical Center, Sölvegatan 39, Lund.
defense date
2000-06-06 10:15:00
external identifiers
  • other:ISRN: LUNKDL/(NKBK-1064)/1-116/2000
language
English
LU publication?
yes
additional info
Article: Protein Partitioning in Weakly Charged Polymer/Surfactant Aqueous Two-Phase Systems, Ulf Sivars, Karin Bergfeldt, Lennart Piculell and Folke Tjerneld, Journal of Chromatography B, 680 (1996) 43-53. Article: Mechanisms of Phase Behavior and Protein Partitioning in Detergent/Polymer Aqueous Two-Phase Systems for Purification of Integral Membrane Proteins, Ulf Sivars and Folke Tjerneld, Biochimica et Biophysica Acta, 1474 2 (2000) 133-146. Article: Affinity Partitioning of a Poly(histidine) Tagged Integral Membrane, Cytochrome bo3 Ubiquinol Oxidase from E. coli in Detergent/Polymer Aqueous Two-Phase System Containing Metal Chelating Polymer, Ulf Sivars, Jeff Abramson, So Iwata and Folke Tjerneld, Journal of Chromatography B, 2000 (in press) Article: Purification of an integral membrane protein cytochrome bo3 ubiquinol oxidase from Escherichia coli membranes by affinity partitioning in polymer induced micelle extraction systems,Ulf Sivars, Viveka Dolby, So Iwata and Folke Tjerneld, (manuscript) Article: Purification of amphiphilic fusion protein in robust polymer induced micelle extraction systems and back-extraction by addition of EOPO-copolymers, Anna Collén, Josefine Persson, Markus Linder, Tiina Nakari-Setälä, Michael Bailey, Merja Penttilä, Folke Tjerneld and Ulf Sivars (manuscript).
id
3c77cf97-3269-4e04-b311-d9855542517a (old id 40586)
date added to LUP
2016-04-04 11:10:55
date last changed
2018-11-21 21:03:11
@phdthesis{3c77cf97-3269-4e04-b311-d9855542517a,
  abstract     = {Increased understanding of membrane proteins is important for characterization of biochemical processes. Improved membrane protein isolation methods is a key issue for effective functional and structural determination of the large amount of unknown membrane proteins.<br/><br>
<br/><br>
In this thesis, a novel approach towards selective membrane protein purification is introduced. Polymer induced micelle extraction (PIME) systems are formed in mixtures between nonionic detergents and water-soluble polymers. Over a critical concentration the detergent/polymer/water mixture separates into two phases and forms a detergent-rich and a polymer-rich phase. Separation of membrane proteins from cytosolic proteins and insoluble materials is achieved by the large difference in distribution between the phases. In general, membrane proteins are extracted into the micelle-enriched phase, while water-soluble proteins partitions in the polymer-rich phase. Membranes can be solubilized directly into the PIME system at low temperature with many commonly used nonionic detergents. The developed micelle-based extraction system is suggested to replace the traditional solubilization step in membrane protein purification. A combined solubilization and primary purification of the target proteins can be obtained. Such smart solubilization in PIME systems was utilized to pre-fractionate membrane proteins prior to detection of a putative membrane bound receptor.<br/><br>
<br/><br>
The partitioning and phase separation mechanism in the PIME systems was examined in detail and explained in a thermodynamic context. An understanding how to optimize the system for membrane protein extraction was gained. Several approaches to further increase the separation between hydrophobic and hydrophilic proteins was studied such as addition of affinity ligands, salts and ionic detergents. A novel high-resolution method was developed, called affinity PIME systems. A selective membrane protein extraction system was obtained by affinity partitioning of the target membrane protein into the polymer-rich phase, while contaminating membrane proteins remained in the opposite micelle-rich phase. The concept was successfully demonstrated by metal affinity purification of the His-tagged integral membrane protein, cytochrome bo3 ubiquinol oxidase from Escherichia coli membranes. Affinity PIME systems should be of great importance for a fast purification of structural intact membrane proteins due the mild and selective properties of the system.<br/><br>
<br/><br>
PIME systems can be applied for purification of amphiphilic fusion proteins. An effective purification of the amphiphilic fusion protein endoglucanase I-hydrophobin I was obtained from a Trichoderma reesei fermentation filtrate. A method was developed for removal of detergent from the purified fusion protein.},
  author       = {Sivars, Ulf},
  language     = {eng},
  publisher    = {Ulf Sivars, Department of Biochemistry, Center for Chemistry and Chemical Engineering, Lund University},
  school       = {Lund University},
  title        = {Selective extraction systems for detection and purification of membrane proteins},
  year         = {2000},
}