High-throughput proteomics: A flexible and efficient pipeline for protein production

被引:15
作者
Doyle, SA [1 ]
Murphy, MB [1 ]
Massi, JM [1 ]
Richardson, PM [1 ]
机构
[1] US DOE, Joint Genome Inst, Walnut Creek, CA 94598 USA
关键词
high-throughput; protein purification; ligation-independent cloning;
D O I
10.1021/pr025554a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Many studies that aim to characterize the proteome require the production of pure protein in a high-throughput format. We have developed a system for high-throughput subcloning, protein expression and purification that is simple, fast, and inexpensive. We utilized ligation-independent cloning with a custom-designed vector and developed an expression screen to test multiple parameters for optimal protein production in E. coli. A 96-well format purification protocol that produced microgram quantities of pure protein was also developed.
引用
收藏
页码:531 / 536
页数:6
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