The alliance for cellular signaling plasmid collection: A flexible resource for protein localization studies and signaling pathway analysis

被引:14
作者
Zavzavadjian, Joelle R.
Couture, Sam
Park, Wei Sun
Whalen, James
Lyon, Stephen
Lee, Genie
Fung, Eileen
Mi, Qingli
Liu, Jamie
Wall, Estelle
Santat, Leah
Dhandapani, Kavitha
Kivork, Christine
Driver, Adrienne
Zhu, Xiaocui
Chang, Mi Sook
Randhawa, Baljinder
Gehrig, Elizabeth
Bryan, Heather
Verghese, Mary
Maer, Andreia
Saunders, Brian
Ning, Yuhong
Subramaniam, Shankar
Meyer, Tobias
Simon, Melvin I.
O'Rourke, Nancy
Chandy, Grischa
Fraser, Iain D. C.
机构
[1] CALTECH, Div Biol, Alliance Cellular Signaling, Pasadena, CA 91125 USA
[2] CALTECH, Mol Biol Lab, Pasadena, CA 91125 USA
[3] Stanford Univ, Microscopy Lab, Palo Alto, CA 94305 USA
[4] Univ Calif San Diego, Bioinformat & Data Coordinat Lab, La Jolla, CA 92093 USA
关键词
ORFEOME; CLONING; KINASE; GENOMICS; ACTIVATION; PLATFORM; GATEWAY; BIOLOGY; MAP;
D O I
10.1074/mcp.M600437-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cellular responses to inputs that vary both temporally and spatially are determined by complex relationships between the components of cell signaling networks. Analysis of these relationships requires access to a wide range of experimental reagents and techniques, including the ability to express the protein components of the model cells in a variety of contexts. As part of the Alliance for Cellular Signaling, we developed a robust method for cloning large numbers of signaling ORFs into Gateway (R) entry vectors, and we created a wide range of compatible expression platforms for proteomics applications. To date, we have generated over 3000 plasmids that are available to the scientific community via the American Type Culture Collection. We have established a website at www.signaling-gateway.org/data/plasmid/ that allows users to browse, search, and blast Alliance for Cellular Signaling plasmids. The collection primarily contains murine signaling ORFs with an emphasis on kinases and G protein signaling genes. Here we describe the cloning, databasing, and application of this proteomics resource for large scale subcellular localization screens in mammalian cell lines.
引用
收藏
页码:413 / 424
页数:12
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