High-throughput crystallography at an affordable cost: The TB Structural Genomics Consortium Crystallization Facility

被引:50
作者
Rupp, B [1 ]
机构
[1] Lawrence Livermore Natl Lab, Macromol Crystallog & TB Struct Genom Consortium, Livermore, CA 94551 USA
关键词
D O I
10.1021/ar020021t
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The crystallization facility of the TB Structural Genomics Consortium, one of nine P50 structural genomics centers sponsored by the National Institutes of Health, provides TB consortium members with automated crystallization, data collection, and basic molecular replacement structure solution up to bias-minimized maps. In contrast to venture capital -funded commercial enterprises, the TB consortium facilities are decentralized and aim to develop high-throughput crystallography methods and automation on a comparatively small budget. In addition to financial constraints, the logistics and organization of a production environment differ considerably from academic settings. The TB Structural Genomics Consortium crystallization facility may thus provide a model for cost-effective, efficient high-throughput crystallography. Processes and methods presented in this review should assist academic institutions planning to invest in high-throughput structural biology to assess both the rewards and risks of establishing structural genomics programs.
引用
收藏
页码:173 / 181
页数:9
相关论文
共 42 条
[1]   Extending the limits of molecular replacement through combined simulated annealing and maximum-likelihood refinement [J].
Adams, PD ;
Pannu, NS ;
Read, RJ ;
Brunger, AT .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1999, 55 :181-190
[2]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[3]  
BRICOGNE G, 2002, ICCBM9 JEN MARC 23 2
[4]  
CARTER CW, 1979, J BIOL CHEM, V254, P2219
[5]  
CARTER CW, 1999, CRYSTALLIZATION NUCL
[6]   Comparative studies of protein crystallization by vapour-diffusion and microbatch techniques [J].
Chayen, NE .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 1998, 54 :8-15
[7]   Crystal engineering:: deletion mutagenesis of the 24 kDa fragment of the DNA gyrase B subunit from Staphylococcus aureus [J].
Dale, GE ;
Kostrewa, D ;
Gsell, B ;
Stieger, M ;
D'Arcy, A .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1999, 55 :1626-1629
[8]   CRYSTALLIZING PROTEINS - A RATIONAL APPROACH [J].
DARCY, A .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :469-471
[9]  
Dauter Z, 2001, INT TABLES CRYSTALLO, VF, P177
[10]   Protein production: feeding the crystallographers and NMR spectroscopists [J].
Edwards, AM ;
Arrowsmith, CH ;
Christendat, D ;
Dharamsi, A ;
Friesen, JD ;
Greenblatt, JF ;
Vedadi, M .
NATURE STRUCTURAL BIOLOGY, 2000, 7 (Suppl 11) :970-972