HIGH-THROUGHPUT SCREENING OF BACTERIAL PROTEIN LOCALIZATION

被引:3
|
作者
Werner, John N. [1 ]
Gitai, Zemer [1 ]
机构
[1] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
来源
METHODS IN ENZYMOLOGY, VOL 471: TWO-COMPONENT SIGNALING SYSTEMS, PART C | 2010年 / 471卷
关键词
ORFEOME CLONING; GLOBAL ANALYSIS; PLATFORM; BIOLOGY; PARTS; GENE;
D O I
10.1016/S0076-6879(10)71011-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ever-increasing number of sequenced genomes and subsequent sequence-based analysis has provided tremendous insight into cellular processes; however, the ability to experimentally manipulate this genomic information in the laboratory requires the development of new high-throughput methods. To translate this genomic information into information on protein function, molecular and cell biological techniques are required. One strategy to gain insight into protein function is to observe where each specific protein is subcellularly localized. We have developed a pipeline of methods that allows rapid, efficient, and scalable gene cloning, imaging, and image analysis. This work focuses on a high-throughput screen of the Caulobacter crescentus proteome to identify proteins with unique subcellular localization patterns. The cloning, imaging, and image analysis techniques described here are applicable to any organism of interest.
引用
收藏
页码:185 / 204
页数:20
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