An approach to rapid protein crystallization using nanodroplets

被引:211
作者
Santarsiero, BD
Yegian, DT
Lee, CC
Spraggon, G
Gu, J
Scheibe, D
Uber, DC
Cornell, EW
Nordmeyer, RA
Kolbe, WF
Jin, J
Jones, AL
Jaklevic, JM
Schultz, PG
Stevens, RC
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[2] Novartis Res Fdn, Genom Inst, San Diego, CA 92121 USA
[3] EO Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[4] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[5] Joint Ctr Struct Genom, La Jolla, CA 92037 USA
关键词
D O I
10.1107/S0021889802001474
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An approach that enables up to a two order of magnitude reduction in the amount of protein required and a tenfold reduction in the amount of time required for vapor-diffusion protein crystallization is reported. A prototype high-throughput automated system was used for the production of diffraction-quality crystals for a variety of proteins from a screen of 480 conditions using drop volumes as small as 20 nL. This approach results in a significant reduction in the time and cost of protein structure determination, and allows for larger and more efficient screens of crystallization parameter space. The ability to produce diffraction-quality crystals rapidly with minimal quantities of protein enables high-throughput efforts in structural genomics and structure-based drug discovery.
引用
收藏
页码:278 / 281
页数:4
相关论文
共 18 条
[11]  
McPherson A., 1999, CRYSTALLIZATION BIOL
[12]   X-ray structure of bacteriorhodopsin at 2.5 angstroms from microcrystals grown in lipidic cubic phases [J].
PebayPeyroula, E ;
Rummel, G ;
Rosenbusch, JP ;
Landau, EM .
SCIENCE, 1997, 277 (5332) :1676-1681
[13]   Protein microcrystals and the design of a microdiffractometer: current experience and plans at EMBL and ESRF/ID13 [J].
Perrakis, A ;
Cipriani, F ;
Castagna, JC ;
Claustre, L ;
Burghammer, M ;
Riekel, C ;
Cusack, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1999, 55 :1765-1770
[14]   A rational approach towards successful crystallization and crystal treatment of human cytomegalovirus protease and its inhibitor complex [J].
Qian, CG ;
Lagacé, L ;
Massariol, MJ ;
Chabot, C ;
Yoakim, C ;
Déziel, R ;
Tong, L .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2000, 56 :175-180
[15]   Optimization of the critical nuclear size for protein crystallization: a note [J].
Saridakis, E .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2000, 56 :106-108
[16]   SOLVENT EVAPORATION RATES IN THE CLOSED CAPILLARY VAPOR DIFFUSION METHOD OF PROTEIN CRYSTAL-GROWTH [J].
SIBILLE, L ;
CLUNIE, JC ;
BAIRD, JK .
JOURNAL OF CRYSTAL GROWTH, 1991, 110 (1-2) :80-88
[17]   High-throughput protein crystallization [J].
Stevens, RC .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2000, 10 (05) :558-563
[18]  
Weber PC, 1997, METHOD ENZYMOL, V276, P13, DOI 10.1016/S0076-6879(97)76048-8