AlphaScreen®-Based Characterization of the Bifunctional Kinase/RNase IRE1α: A Novel and Atypical Drug Target

被引:12
作者
Bouchecareilh, Marion [1 ,2 ]
Caruso, Marie-Elaine [1 ]
Roby, Philippe [3 ]
Parent, Stephane [3 ]
Rouleau, Nathalie [3 ]
Taouji, Said [1 ]
Pluquet, Olivier [1 ]
Bosse, Roger [3 ]
Moenner, Michel [2 ]
Chevet, Eric [1 ]
机构
[1] INSERM, U889, F-33076 Bordeaux, France
[2] INSERM, U920, F-33076 Bordeaux, France
[3] PerkinElmer Biosignal Inc, Montreal, PQ, Canada
关键词
endoplasmic reticulum; stress; IRE1; AlphaScreen (R); UNFOLDED PROTEIN RESPONSE; ENDOPLASMIC-RETICULUM STRESS; MESSENGER-RNA; IRE1; ACTIVATION; INTEGRATION; PATHWAY; CELLS; ER;
D O I
10.1177/1087057110363823
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Assay technologies that were originally developed for high-throughput screening (HTS) have recently proven useful in drug discovery for activities located upstream (target identification and validation) and downstream (ADMET) of HTS. Here the authors investigated and characterized the biological properties of a novel target, IRE1 alpha, a bifunctional kinase/RNase stress sensor of the endoplasmic reticulum (ER). They have developed a novel assay platform using the HTS technology AlphaScreen(R) to monitor the dimerization/oligomerization and phosphorylation properties of the cytosolic domain of IRE1a. They show in vitro that dimerization/oligomerization of the cytosolic domain of IRE1 correlated with the autophosphorylation ability of this domain and its endoribonuclease activity toward XBP1 mRNA. Using orthogonal in vitro and cell-based approaches, the authors show that the results obtained using AlphaScreen(R) were biologically relevant. Preliminary characterization of assay robustness indicates that both AlphaScreen(R) assays should be useful in HTS for the identification of IRE1 activity modulators. (Journal of Biomolecular Screening 2010:406-417)
引用
收藏
页码:406 / 417
页数:12
相关论文
共 26 条
[1]   Messenger RNA targeting to endoplasmic reticulum stress signalling sites [J].
Aragon, Tomas ;
van Anken, Eelco ;
Pincus, David ;
Serafimova, Iana M. ;
Korennykh, Alexei V. ;
Rubio, Claudia A. ;
Walter, Peter .
NATURE, 2009, 457 (7230) :736-U9
[2]   GTPase-mediated regulation of the unfolded protein response in Caenorhabditis elegans is dependent on the AAA+ ATPase CDC-48 [J].
Caruso, Marie-Elaine ;
Jenna, Sarah ;
Bouchecareilh, Marion ;
Baillie, David L. ;
Boismenu, Daniel ;
Halawani, Dalia ;
Latterich, Martin ;
Chevet, Eric .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (13) :4261-4274
[3]   Biochemical clustering of monomeric GTPases of the Ras superfamily [J].
Caruso, ME ;
Jenna, S ;
Beaulne, S ;
Lee, EH ;
Bergeron, A ;
Chauve, C ;
Roby, P ;
Rual, JF ;
Hill, DE ;
Vidal, M ;
Bossé, R ;
Chevet, E .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (07) :936-944
[4]   The endoplasmic reticulum: integration of protein folding, quality control, signaling and degradation [J].
Chevet, E ;
Cameron, PH ;
Pelletier, MF ;
Thomas, DY ;
Bergeron, JJM .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2001, 11 (01) :120-124
[5]   On the mechanism of sensing unfolded protein in the endoplasmic reticulum [J].
Credle, JJ ;
Finer-Moore, JS ;
Papa, FR ;
Stroud, RM ;
Walter, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (52) :18773-18784
[6]   IRE1 signaling is essential for ischemia-induced vascular endothelial growth factor-a expression and contributes to angiogenesis and tumor growth in vivo [J].
Drogat, Benjamin ;
Auguste, Patrick ;
Nguyen, Duc Thang ;
Bouchecareilh, Marion ;
Pineau, Raphael ;
Nalbantoglu, Josephine ;
Kaufman, Randal J. ;
Chevet, Eric ;
Bikfalvi, Andreas ;
Moenner, Michel .
CANCER RESEARCH, 2007, 67 (14) :6700-6707
[7]   IRE1α Kinase Activation Modes Control Alternate Endoribonuclease Outputs to Determine Divergent Cell Fates [J].
Han, Dan ;
Lerner, Alana G. ;
Vande Walle, Lieselotte ;
Upton, John-Paul ;
Xu, Weihong ;
Hagen, Andrew ;
Backes, Bradley J. ;
Oakes, Scott A. ;
Papa, Feroz R. .
CELL, 2009, 138 (03) :562-575
[8]   Fine-Tuning of the Unfolded Protein Response: Assembling the IRE1α Interactome [J].
Hetz, Claudio ;
Glimcher, Laurie H. .
MOLECULAR CELL, 2009, 35 (05) :551-561
[9]   Chemical Biology Investigation of Cell Death Pathways Activated by Endoplasmic Reticulum Stress Reveals Cytoprotective Modulators of ASK1 [J].
Kim, InKi ;
Shu, Chih-Wen ;
Xu, Wenjie ;
Shiau, Chung-Wai ;
Grant, Daniel ;
Vasile, Stefan ;
Cosford, Nicholas D. P. ;
Reed, John C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (03) :1593-1603
[10]   The unfolded protein response signals through high-order assembly of Ire1 [J].
Korennykh, Alexei V. ;
Egea, Pascal F. ;
Korostelev, Andrei A. ;
Finer-Moore, Janet ;
Zhang, Chao ;
Shokat, Kevan M. ;
Stroud, Robert M. ;
Walter, Peter .
NATURE, 2009, 457 (7230) :687-U2