Protein biophysical properties that correlate with crystallization success in Thermotoga maritima:: Maximum clustering strategy for structural genomics

被引:71
作者
Canaves, JM
Page, R
Wilson, IA
Stevens, RC
机构
[1] Univ Calif San Diego, Ctr Res Biol Syst, La Jolla, CA 92093 USA
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[3] Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
structural genomics; protein properties; expression; crystallization;
D O I
10.1016/j.jmb.2004.09.076
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
Cost and time reduction are two of the driving forces in the development of new strategies for protein crystallization and subsequent structure determination. Here, we report the analysis of the Thermotoga maritima proteome, in which we compare the proteins that were successfully expressed, purified and crystallized versus the rest of the proteome. This set of almost 500 proteins represents one of the largest, internally consistent, protein expression and crystallization datasets available. The analysis shows that individual parameters, such as isoelectric point, sequence length, average hydropathy, low complexity regions (SEG), and combinations of these biophysical properties for crystallized proteins define a distinct subset of the T. maritinia proteome. The distribution profiles of the various biophysical properties in the expression/ crystallization set are then used to extract rules to improve target selection and improve the efficiency and output of structural genomics, as well as general structural biology efforts. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:977 / 991
页数:15
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