Lipids and membrane protein structures

被引:155
作者
Hunte, Carola [1 ]
Richers, Sebastian [2 ]
机构
[1] Univ Leeds, Inst Membrane & Syst Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Max Planck Inst Biophys, Dept Mol Membrane Biol, D-60438 Frankfurt, Germany
关键词
D O I
10.1016/j.sbi.2008.03.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membrane proteins do not work alone. The interaction of proteins with membrane lipids can be highly specific and is often important for full functional and structural integrity of the protein. Providing the appropriate lipid environment is of great importance for the purification and crystallisation of membrane proteins. The lipid content can be modulated by adjusting purification protocols or by adding back native or non-native lipids. Lipids can facilitate crystallisation by stabilising the protein and by providing lattice contacts. Of special interest is the crystallisation in lipidic cubic phase and with bicelles, as they appear to provide a membrane-like environment. These strategies have been instrumental for recent successful structure determinations of a human G-protein-coupled receptor, the beta(2)-adrenergic receptor. Lipid supplementation can also help to obtain membrane protein structures in a native conformation, as shown for voltage-gated potassium channels. Membrane protein structures, especially those derived from lipid-enriched preparations, contain bound lipid molecules. Specific protein-lipid interactions not only require careful evaluation and interpretation, but also permit a directed approach to elucidate the structural and/or functional role of these interactions.
引用
收藏
页码:406 / 411
页数:6
相关论文
共 43 条
[11]   A peptide derived from a beta(2)-adrenergic receptor transmembrane domain inhibits both receptor dimerization and activation [J].
Hebert, TE ;
Moffett, S ;
Morello, JP ;
Loisel, TP ;
Bichet, DG ;
Barret, C ;
Bouvier, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (27) :16384-16392
[12]   Specific protein-lipid interactions in membrane proteins [J].
Hunte, C .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2005, 33 :938-942
[13]   X-ray structure of a voltage-dependent K+ channel [J].
Jiang, YX ;
Lee, A ;
Chen, JY ;
Ruta, V ;
Cadene, M ;
Chait, BT ;
MacKinnon, R .
NATURE, 2003, 423 (6935) :33-41
[14]   Crystallization of a mammalian membrane protein overexpressed in Saccharomyces cerevisiae [J].
Jidenko, M ;
Nielsen, RC ;
Sorensen, TLM ;
Moller, JV ;
le Maire, M ;
Nissen, P ;
Jaxel, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (33) :11687-11691
[15]   PURIFICATION AND CHARACTERIZATION OF (NA++K+)-ATPASE .3. PURIFICATION FROM OUTER MEDULLA OF MAMMALIAN KIDNEY AFTER SELECTIVE REMOVAL OF MEMBRANE COMPONENTS BY SODIUM DODECYLSULFATE [J].
JORGENSEN, PL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1974, 356 (01) :36-52
[16]   Redox-linked protonation state changes in cytochrome bc1 identified by Poisson-Boltzmann electrostatics calculations [J].
Klingen, Astrid R. ;
Palsdottir, Hildur ;
Hunte, Carola ;
Ullmann, G. Matthias .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2007, 1767 (03) :204-221
[17]   Predicting transmembrane protein topology with a hidden Markov model: Application to complete genomes [J].
Krogh, A ;
Larsson, B ;
von Heijne, G ;
Sonnhammer, ELL .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 305 (03) :567-580
[18]   Structure of the cytochrome b6f complex of oxygenic photosynthesis:: Tuning the cavity [J].
Kurisu, G ;
Zhang, HM ;
Smith, JL ;
Cramer, WA .
SCIENCE, 2003, 302 (5647) :1009-1014
[19]   Lipidic cubic phases: A novel concept for the crystallization of membrane proteins [J].
Landau, EM ;
Rosenbusch, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14532-14535
[20]   Specific roles of protein-phospholipid interactions in the yeast cytochrome bc1 complex structure [J].
Lange, C ;
Nett, JH ;
Trumpower, BL ;
Hunte, C .
EMBO JOURNAL, 2001, 20 (23) :6591-6600