Overcoming the challenges of membrane protein crystallography

被引:346
作者
Carpenter, Elisabeth P. [1 ,2 ,3 ]
Beis, Konstantinos [1 ,2 ,3 ]
Cameron, Alexander D. [1 ,2 ,3 ]
Iwata, So [1 ,2 ,3 ,4 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Diamond Light Source Ltd, Membrane Prot Lab, Didcot OX11 ODE, Oxon, England
[2] Univ London Imperial Coll Sci Technol & Med, Div Mol Biosci, Membrane Prot Crystallog Grp, London SW7 2AZ, England
[3] Univ London Imperial Coll Sci Technol & Med, Membrane Prot Lab, London SW7 2AZ, England
[4] Kyoto Univ, ERATO Human Receptor Crystallog Project, Grad Sch Med, Sakyo Ku, Kyoto 6068501, Japan
关键词
D O I
10.1016/j.sbi.2008.07.001
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 protein structural biology is still a largely unconquered area, given that approximately 25% of all proteins are membrane proteins and yet less than 150 unique structures are available. Membrane proteins have proven to be difficult to study owing to their partially hydrophobic surfaces, flexibility and lack of stability. The field is now taking advantage of the high-throughput revolution in structural biology and methods are emerging for effective expression, solubilisation, purification and crystallisation of membrane proteins. These technical advances will lead to a rapid increase in the rate at which membrane protein structures are solved in the near future.
引用
收藏
页码:581 / 586
页数:6
相关论文
共 61 条
[1]   Microscale fluorescent thermal stability assay for membrane proteins [J].
Alexandrov, Alexander I. ;
Mileni, Mauro ;
Chien, Ellen Y. T. ;
Hanson, Michael A. ;
Stevens, Raymond C. .
STRUCTURE, 2008, 16 (03) :351-359
[2]   Structure of human monoamine oxidase B, a drug target for the treatment of neurological disorders [J].
Binda, C ;
Newton-Vinson, P ;
Hubálek, F ;
Edmondson, DE ;
Mattevi, A .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (01) :22-26
[3]   Structural genomics: inside a protein structure initiative center [J].
Blow, Nathan .
NATURE METHODS, 2008, 5 (02) :203-206
[4]   Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling [J].
Bracey, MH ;
Hanson, MA ;
Masuda, KR ;
Stevens, RC ;
Cravatt, BF .
SCIENCE, 2002, 298 (5599) :1793-1796
[5]   A robotic system for crystallizing membrane and soluble proteins in lipidic mesophases [J].
Cherezov, V ;
Peddi, A ;
Muthusubramaniam, L ;
Zheng, YF ;
Caffrey, M .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2004, 60 :1795-1807
[6]   In meso structure of the cobalamin transporter, BtuB, at 1.95 Å resolution [J].
Cherezov, V. ;
Yamashita, E. ;
Liu, W. ;
Zhalnina, M. ;
Cramer, W. A. ;
Caffrey, M. .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 364 (04) :716-734
[7]   High-resolution crystal structure of an engineered human β2-adrenergic G protein-coupled receptor [J].
Cherezov, Vadim ;
Rosenbaum, Daniel M. ;
Hanson, Michael A. ;
Rasmussen, Soren G. F. ;
Thian, Foon Sun ;
Kobilka, Tong Sun ;
Choi, Hee-Jung ;
Kuhn, Peter ;
Weis, William I. ;
Kobilka, Brian K. ;
Stevens, Raymond C. .
SCIENCE, 2007, 318 (5854) :1258-1265
[8]   Colony filtration blot:: a new screening method for soluble protein expression in Escherichia coli [J].
Cornvik, T ;
Dahlroth, SL ;
Magnusdottir, A ;
Herman, MD ;
Knaust, R ;
Ekberg, M ;
Nordlund, P .
NATURE METHODS, 2005, 2 (07) :507-509
[9]   A monoclonal antibody for G protein-coupled receptor crystallography [J].
Day, Peter W. ;
Rasmussen, Soren G. F. ;
Parnot, Charles ;
Fung, Juan Jose ;
Masood, Asna ;
Kobilka, Tong Sun ;
Yao, Xiao-Jie ;
Choi, Hee-Jung ;
Weis, William I. ;
Rohrer, Daniel K. ;
Kobilka, Brian K. .
NATURE METHODS, 2007, 4 (11) :927-929
[10]   Three-dimensional structure of human monoamine oxidase A (MAO A): Relation to the structures of rat MAO A and human MAO B [J].
De Colibus, L ;
Li, M ;
Binda, C ;
Lustig, A ;
Edmondson, DE ;
Mattevi, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12684-12689