Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. Signal., 15 May 2012
Vol. 5, Issue 224, p. rs4
[DOI: 10.1126/scisignal.2002612]
RESEARCH RESOURCES
Editor's Summary
Scaling Up Drug Discovery with Functional Genomics
The ability to perform high-throughput gain- and loss-of-function screens with mammalian cells in culture is a potentially important tool for exploring both basic cellular biology and drug discovery. Wood et al. describe a method they call "MicroSCALE screening," which overcomes several technical limitations and enables rapid, high-throughput screening of mammalian cells plated on patterned surfaces and infected with viral libraries to achieve overexpression of specific proteins or with RNA interference vectors to achieve protein knockdown. Their procedure overcomes issues related to cellular migration and lack of uniformity in cellular infection. In addition, the authors devised simple, inexpensive image-based screening methods that allow rapid data collection. With this MicroSCALE screening system, Wood et al. overexpressed a kinome library and identified proteins that influenced the sensitivity of melanoma cells to various clinically used antineoplastic agents. Thus, this method should advance drug discovery and enhance identification of effective combination therapies.
Citation: K. C. Wood, D. J. Konieczkowski, C. M. Johannessen, J. S. Boehm, P. Tamayo, O. B. Botvinnik, J. P. Mesirov, W. C. Hahn, D. E. Root, L. A. Garraway, D. M. Sabatini, MicroSCALE Screening Reveals Genetic Modifiers of Therapeutic Response in Melanoma. Sci. Signal.5, rs4 (2012).
The editors suggest the following Related Resources on Science sites:
In Science Signaling
PERSPECTIVES
Michael B. Yaffe (2 April 2013) Sci. Signal.6 (269), pe13.
[DOI: 10.1126/scisignal.2003684] |Abstract »|Full Text »|PDF »
EDITORIAL GUIDES
Nancy R. Gough (26 March 2013) Sci. Signal.6 (268), eg3.
[DOI: 10.1126/scisignal.2004149] |Abstract »|Full Text »|PDF »
PODCASTS
Friedegund Meier and Annalisa M. VanHook (29 January 2013) Sci. Signal.6 (260), pc3.
[DOI: 10.1126/scisignal.2003968] |Abstract »|Full Text »|Podcast »
RESEARCH ARTICLES
Daniela Beck, Heike Niessner, Keiran S. M. Smalley, Keith Flaherty, Kim H. T. Paraiso, Christian Busch, Tobias Sinnberg, Sophie Vasseur, Juan Lucio Iovanna, Stefan Drießen, Björn Stork, Sebastian Wesselborg, Martin Schaller, Tilo Biedermann, Jürgen Bauer, Konstantinos Lasithiotakis, Benjamin Weide, Jürgen Eberle, Birgit Schittek, Dirk Schadendorf, Claus Garbe, Dagmar Kulms, and Friedegund Meier (29 January 2013) Sci. Signal.6 (260), ra7.
[DOI: 10.1126/scisignal.2003057] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
PERSPECTIVES
Edward C. Stites (16 October 2012) Sci. Signal.5 (246), pe46.
[DOI: 10.1126/scisignal.2003354] |Abstract »|Full Text »|PDF »
Woo-Jeong Jeong, Juyong Yoon, Jong-Chan Park, Soung-Hoon Lee, Seung-Hoon Lee, Saluja Kaduwal, Hoguen Kim, Jong-Bok Yoon, and Kang-Yell Choi (10 April 2012) Sci. Signal.5 (219), ra30.
[DOI: 10.1126/scisignal.2002242] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
RESEARCH ARTICLES
Travis L. Biechele, Rima M. Kulikauskas, Rachel A. Toroni, Olivia M. Lucero, Reyna D. Swift, Richard G. James, Nick C. Robin, David W. Dawson, Randall T. Moon, and Andy J. Chien (10 January 2012) Sci. Signal.5 (206), ra3.
[DOI: 10.1126/scisignal.2002274] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »