Novel buffer systems for macromolecular crystallization

被引:111
作者
Newman, J
机构
[1] Encinitas, CA 92024
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2004年 / 60卷
关键词
D O I
10.1107/S0907444903029640
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In protein crystallization, screening is initially performed to obtain an indication of the conditions under which a macromolecule might crystallize. These preliminary conditions are then optimized to produce (in a perfect world) well diffracting crystals; this process of optimization often involves fine grid screening around the initial conditions. An issue in optimization is to find factors which are independent, so as to simplify the analysis of the results of optimization trials. This is necessarily difficult with buffers, as a buffer and its pH range tend to be very highly correlated. Multi-buffer systems for pH modulation are presented which enable a broad pH range to be sampled without changing the chemical composition of the buffering component.
引用
收藏
页码:610 / 612
页数:3
相关论文
共 4 条
  • [1] High-performance chromatofocusing using linear and concave pH gradients formed with simple buffer mixtures I. Effect of buffer composition on the gradient shape
    Bates, RC
    Kang, XZ
    Frey, DD
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2000, 890 (01) : 25 - 36
  • [2] The Protein Data Bank
    Berman, HM
    Westbrook, J
    Feng, Z
    Gilliland, G
    Bhat, TN
    Weissig, H
    Shindyalov, IN
    Bourne, PE
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (01) : 235 - 242
  • [3] SPARSE-MATRIX SAMPLING - A SCREENING METHOD FOR CRYSTALLIZATION OF PROTEINS
    JANCARIK, J
    KIM, SH
    [J]. JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1991, 24 : 409 - 411
  • [4] Databases in protein Crystallography
    Kleywegt, GJ
    Jones, TA
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 1998, 54 : 1119 - 1131