Membrane proteins, lipids and detergents: not just a soap opera

@article{citeulike:941956, abstract = {Studying membrane proteins represents a major challenge in protein biochemistry, with one of the major difficulties being the problems encountered when working outside the natural lipid environment. In vitro studies such as crystallization are reliant on the successful solubilization or reconstitution of membrane proteins, which generally involves the careful selection of solubilizing detergents and mixed lipid/detergent systems. This review will concentrate on the methods currently available for efficient reconstitution and solubilization of membrane proteins through the use of detergent micelles, mixed lipid/detergent micelles and bicelles or liposomes. We focus on the relevant molecular properties of the detergents and lipids that aid understanding of these processes. A significant barrier to membrane protein research is retaining the stability and function of the protein during solubilization, reconstitution and crystallization. We highlight some of the lessons learnt from studies of membrane protein folding in vitro and give an overview of the role that lipids can play in stabilizing the proteins.}, author = {Seddon, Annela M. and Curnow, Paul and Booth, Paula J. }, booktitle = {Lipid-Protein Interactions}, citeulike-article-id = {941956}, doi = {10.1016/j.bbamem.2004.04.011}, journal = {Biochimica et Biophysica Acta (BBA) - Biomembranes}, keywords = {detergent, lipid, membrane, protein}, month = {November}, number = {1-2}, pages = {105--117}, posted-at = {2006-11-13 17:52:31}, priority = {4}, title = {Membrane proteins, lipids and detergents: not just a soap opera}, url = {http://dx.doi.org/10.1016/j.bbamem.2004.04.011}, volume = {1666}, year = {2004} }

TY - JOUR ID - citeulike:941956 L3 - citeulike-article-id:941956 TI - Membrane proteins, lipids and detergents: not just a soap opera T2 - Lipid-Protein Interactions JF - Biochimica et Biophysica Acta (BBA) - Biomembranes VL - 1666 IS - 1-2 SP - 105 EP - 117 N2 - Studying membrane proteins represents a major challenge in protein biochemistry, with one of the major difficulties being the problems encountered when working outside the natural lipid environment. In vitro studies such as crystallization are reliant on the successful solubilization or reconstitution of membrane proteins, which generally involves the careful selection of solubilizing detergents and mixed lipid/detergent systems. This review will concentrate on the methods currently available for efficient reconstitution and solubilization of membrane proteins through the use of detergent micelles, mixed lipid/detergent micelles and bicelles or liposomes. We focus on the relevant molecular properties of the detergents and lipids that aid understanding of these processes. A significant barrier to membrane protein research is retaining the stability and function of the protein during solubilization, reconstitution and crystallization. We highlight some of the lessons learnt from studies of membrane protein folding in vitro and give an overview of the role that lipids can play in stabilizing the proteins. KW - detergent KW - lipid KW - membrane KW - protein AU - Seddon, Annela AU - Curnow, Paul AU - Booth, Paula PY - 2004/11/03/ UR - http://dx.doi.org/10.1016/j.bbamem.2004.04.011 ER -