The Alliance for Cellular Signaling Plasmid Collection

Joelle R. Zavzavadjian(California Institute of Technology), Sam Couture(California Institute of Technology), Wei Sun Park(California Institute of Technology), James H. Whalen(California Institute of Technology), Stephen Lyon(California Institute of Technology), Genie Lee(California Institute of Technology), Eileen Fung(California Institute of Technology), Qingli Mi(California Institute of Technology), Jamie Liu(California Institute of Technology), Estelle A. Wall(California Institute of Technology), Leah A. Santat(California Institute of Technology), Kavitha Dhandapani(California Institute of Technology), Christine Kivork(California Institute of Technology), Adrienne Driver(California Institute of Technology), Xiaocui Zhu(California Institute of Technology), Mi Sook Chang(California Institute of Technology), Baljinder Randhawa(California Institute of Technology), Elizabeth Gehrig(California Institute of Technology), Heather M. Bryan(California Institute of Technology), Mary Verghese(California Institute of Technology), Andreia M Maer(California Institute of Technology), Brian Saunders(California Institute of Technology), Yuhong Ning(California Institute of Technology), Shankar Subramaniam(California Institute of Technology), Tobias Meyer(California Institute of Technology), Melvin I. Simon(California Institute of Technology), Nancy O’Rourke(California Institute of Technology), Grischa Chandy(California Institute of Technology), Iain D. C. Fraser(California Institute of Technology)
Molecular & Cellular Proteomics
December 27, 2006
Cited by 14Open Access
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Abstract

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 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.


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