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Journal Article

Novel Caspase-Suicide Proteins for Tamoxifen-Inducible Apoptosis

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Wurst,  W.
Max Planck Institute of Psychiatry, Max Planck Society;

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Citation

Chu, Y. Y., Senghaas, N., Köster, R. W., Wurst, W., & Kühn, R. (2008). Novel Caspase-Suicide Proteins for Tamoxifen-Inducible Apoptosis. Genesis, 46(10), 530-536.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-93BF-3
Abstract
Taking advantage of a mutant estrogen receptor ligand binding domain (ER T), we developed novel Caspase fusion proteins for inducible apoptosis. We show that Caspase-ERT2 fusion proteins become specifically activated by the synthetic ligand 4-OH-tamoxifen and rapidly induce apoptotic cell death in human, murine, and zebrafish cells. This novel tool for targeted cell ablation greatly facilitates the generation of disease models as well as developmental and regeneration studies in model organisms. genesis 46:530-536, 2008. (C) 2008 Wiley-Liss, Inc.