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Identification of a small molecule yeast TORC1 inhibitor with a flow cytometry-based multiplex screen
dc.contributor.author | Chen, Jun | |
dc.contributor.author | Young, Susan M. | |
dc.contributor.author | Allen, Chris | |
dc.contributor.author | Seeber, Andrew | |
dc.contributor.author | Péli-Gulli, Marie-Pierre | |
dc.contributor.author | Panchaud, Nicolas | |
dc.contributor.author | Waller, Anna | |
dc.contributor.author | Ursu, Oleg | |
dc.contributor.author | Yao, Tuanli | |
dc.contributor.author | Golden, Jennifer E. | |
dc.contributor.author | Strouse, J. Jacob | |
dc.contributor.author | Carter, Mark B. | |
dc.contributor.author | Kang, Huining | |
dc.contributor.author | Bologa, Cristian G. | |
dc.contributor.author | Foutz, Terry D. | |
dc.contributor.author | Edwards, Bruce S. | |
dc.contributor.author | Peterson, Blake R. | |
dc.contributor.author | Aubé, Jeffrey | |
dc.contributor.author | Werner-Washburne, Margaret | |
dc.contributor.author | Loewith, Robbie J. | |
dc.contributor.author | De Virgilio, Claudio | |
dc.contributor.author | Sklar, Larry A. | |
dc.date.accessioned | 2017-03-30T18:16:04Z | |
dc.date.available | 2017-03-30T18:16:04Z | |
dc.date.issued | 2012-04-20 | |
dc.identifier.citation | Chen, J., Young, S. M., Allen, C., Seeber, A., Péli-Gulli, M.-P., Panchaud, N., … Sklar, L. A. (2012). Identification of a small molecule yeast TORC1 inhibitor with a flow cytometry-based multiplex screen. ACS Chemical Biology, 7(4), 715–722. http://doi.org/10.1021/cb200452r | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/23523 | |
dc.description.abstract | TOR (target of rapamycin) is a serine/threonine kinase, evolutionarily conserved from yeast to human, which functions as a fundamental controller of cell growth. The moderate clinical benefit of rapamycin in mTOR-based therapy of many cancers favors the development of new TOR inhibitors. Here we report a high throughput flow cytometry multiplexed screen using five GFPtagged yeast clones that represent the readouts of four branches of the TORC1 signaling pathway in budding yeast. Each GFP-tagged clone was differentially color-coded and the GFP signal of each clone was measured simultaneously by flow cytometry, which allows rapid prioritization of compounds that likely act through direct modulation of TORC1 or proximal signaling components. A total of 255 compounds were confirmed in dose-response analysis to alter GFP expression in one or more clones. To validate the concept of the high throughput screen, we have characterized CID 3528206, a small molecule most likely to act on TORC1 as it alters GFP expression in all five GFP clones in an analogous manner to rapamycin. We have shown that CID 3528206 inhibited yeast cell growth, and that CID 3528206 inhibited TORC1 activity both in vitro and in vivo with EC50s of 150 nM and 3.9 μM, respectively. The results of microarray analysis and yeast GFP collection screen further support the notion that CID 3528206 and rapamycin modulate similar cellular pathways. Together, these results indicate that the HTS has identified a potentially useful small molecule for further development of TOR inhibitors. | en_US |
dc.publisher | ACS Chem Biol. | en_US |
dc.rights | © 2012 American Chemical Society | en_US |
dc.title | Identification of a small molecule yeast TORC1 inhibitor with a flow cytometry-based multiplex screen | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Yao, Tuanli | |
kusw.kuauthor | Golden, Jennifer E. | |
kusw.kuauthor | Peterson, Blake R. | |
kusw.kuauthor | Aubé, Jeffrey | |
kusw.kudepartment | Specialized Chemistry Center | en_US |
kusw.kudepartment | Medicinal Chemistry | en_US |
dc.identifier.doi | 10.1021/cb200452r | en_US |
dc.identifier.orcid | https://orcid.org/0000-0003-1049-5767 | |
dc.identifier.orcid | https://orcid.org/0000-0002-6813-3710 | |
kusw.oaversion | Scholarly/refereed, author accepted manuscript | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.rights.accessrights | openAccess |