Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here to register for free online access

Sign In to gain access to subscriptions and/or personal tools.
Journal of Biomolecular Screening
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Rouleau, N.
Right arrow Articles by Bossé, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rouleau, N.
Right arrow Articles by Bossé, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Development of a Versatile Platform for Nuclear Receptor Screening Using AlphaScreenTM

Nathalie Rouleau

1744 William, Montreal, Quebec, Canada H3J 1R4. nathalie.rouleau@perkinelmer.com

Sophie Turcotte

Marie-Hélène Mondou

Philippe Roby

Roger Bossé

The interaction between nuclear receptors (NRs) and their coactivators, a key step in transcription regulation, requires a short consensus sequence called the LXXLL motif found in the coactivators’ structure. Using the AlphaScreenTM technology, the authors have taken advantage of this receptor-coactivator interaction to develop a highly sensitive assay to identify and characterize compounds modulating NR activity. Estrogen and retinoic acid receptors were chosen as models to demonstrate the versatility of the AlphaScreen technology: (1) the assay can be designed using different antibodies to capture either full-length receptors or receptor domains that have been tagged, (2) the assay can differentiate between ligands that act as agonists or antagonists because only agonists will allow recruitment of the coactivator sequence–derived peptide, and (3) the assay gives the opportunity to screen for antagonists targeting the ligand-binding site or the dimerization interface between the receptor and the coactivator. Titration of the receptor and biotinylated peptide indicates that AlphaScreen is highly sensitive, requiring nanomolar concentration of reagents. Competition isotherms performed with known receptor antagonists demonstrate that the assay is a useful tool to rank the antagonists according to their order of potency. Overall, the results presented here indicate that the versatility, sensitivity, robustness, and ease of execution of the AlphaScreen NR assay will allow for efficient screening of NR modulators. (Journal of Biomolecular Screening 2003:191-197)

Key Words: nuclear receptors • AlphaScreen • coactivators • LXXLL peptide sequence • estrogen receptor (ER) • retinoic acid receptor (RAR) • ligand-binding domains (LBD)

Journal of Biomolecular Screening, Vol. 8, No. 2, 191-197 (2003)
DOI: 10.1177/1087057103252605


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J Biomol ScreenHome page
J.-h. Zhang, X. Wu, and M. A. Sills
Probing the Primary Screening Efficiency by Multiple Replicate Testing: A Quantitative Analysis of Hit Confirmation and False Screening Results of a Biochemical Assay
J Biomol Screen, October 1, 2005; 10(7): 695 - 704.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
B. Kus, A. Gajadhar, K. Stanger, R. Cho, W. Sun, N. Rouleau, T. Lee, D. Chan, C. Wolting, A. Edwards, et al.
A High Throughput Screen to Identify Substrates for the Ubiquitin Ligase Rsp5
J. Biol. Chem., August 19, 2005; 280(33): 29470 - 29478.
[Abstract] [Full Text] [PDF]


Home page
J Biomol ScreenHome page
A. Von Leoprechting, R. Kumpf, S. Menzel, D. Reulle, R. Griebel, M. J. Valler, and F. H. Buttner
Miniaturization and Validation of a High-Throughput Serine Kinase Assay Using the Alpha Screen Platform
J Biomol Screen, December 1, 2004; 9(8): 719 - 725.
[Abstract] [PDF]