A pedestrian guide to membrane protein crystallization

被引:137
作者
Wiener, MC [1 ]
机构
[1] Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院; 美国国家航空航天局;
关键词
membrane protein; crystallization; detergent; X-ray crystallography;
D O I
10.1016/j.ymeth.2004.03.025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Membrane protein structural biology is a frontier area of modern biomedical research. Twenty to thirty-five percent of the proteins encoded by an organism's genome are integral membrane proteins. Integral membrane proteins, such as channels, transporters, and receptors, are critical components of many fundamental biological processes. Also, many integral membrane proteins are important in biomedical and biotechnological applications; the majority of drug targets are integral membrane proteins. The sharp increase in the number of membrane protein structures over the last several years gives some indication that this field is poised for rather explosive growth as more and more investigators take on membrane protein projects. The purpose of this brief practical review was to take a snapshot of a field at the onset of its likely exponential growth phase, and to lay out the methods that have worked to date for obtaining membrane protein crystals suitable for structure determination by X-ray crystallography. Many of the successful experimental methods are identical to those used for soluble proteins. The major difference, and a non-trivial difference, is the necessity for inclusion of detergents above the critical micelle concentration in the purified membrane protein solution. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:364 / 372
页数:9
相关论文
共 76 条
[1]   CRYSTALLIZATION OF REACTION CENTER FROM RHODOPSEUDOMONAS-SPHAEROIDES - PRELIMINARY CHARACTERIZATION [J].
ALLEN, JP ;
FEHER, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (15) :4795-4799
[2]   A robust, detergent-friendly method for mass spectrometric analysis of integral membrane proteins [J].
Cadene, M ;
Chait, BT .
ANALYTICAL CHEMISTRY, 2000, 72 (22) :5655-5658
[3]   MICELLE FORMATION BY BILE-SALTS - PHYSICAL-CHEMICAL AND THERMODYNAMIC CONSIDERATIONS [J].
CAREY, MC ;
SMALL, DM .
ARCHIVES OF INTERNAL MEDICINE, 1972, 130 (04) :506-+
[4]   MICELLAR PROPERTIES OF DIHYDROXY AND TRIHYDROXY BILE SALTS - EFFECTS OF COUNTERION AND TEMPERATURE [J].
CAREY, MC ;
SMALL, DM .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1969, 31 (03) :382-&
[5]   Stabilization of integral membrane proteins in aqueous solution using fluorinated surfactants [J].
Chabaud, E ;
Barthélémy, P ;
Mora, N ;
Popot, JL ;
Pucci, B .
BIOCHIMIE, 1998, 80 (5-6) :515-530
[6]   Structure of the MscL homolog from Mycobacterium tuberculosis:: A gated mechanosensitive ion channel [J].
Chang, G ;
Spencer, RH ;
Lee, AT ;
Barclay, MT ;
Rees, DC .
SCIENCE, 1998, 282 (5397) :2220-2226
[7]   DnaK and DnaJ facilitated the folding process and reduced inclusion body formation of magnesium transporter CorA overexpressed in Escherichia coli [J].
Chen, Y ;
Song, JM ;
Sui, SF ;
Wang, DN .
PROTEIN EXPRESSION AND PURIFICATION, 2003, 32 (02) :221-231
[8]   Substrate-induced transmembrane signaling in the cobalamin transporter BtuB [J].
Chimento, DP ;
Mohanty, AK ;
Kadner, RJ ;
Wiener, MC .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (05) :394-401
[9]   Crystallization and initial X-ray diffraction of BtuB, the integral membrane cobalamin transporter of Escherichia coli [J].
Chimento, DP ;
Mohanty, AK ;
Kadner, RJ ;
Wiener, MC .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2003, 59 :509-511
[10]  
Christie WW, 2003, LIPID ANAL