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David Engelberg

 
david-engelberg.jpg

Professor David Engelberg
PhD
Principal Investigator
MMID2

Professor
Department of Biological Chemistry
The Hebrew University of Jerusalem

engelber@mail.huji.ac.il
micde@nus.edu.sg
+972 2 6584718
+65 6601 2710

Research Interests

The molecular basis of inflammatory diseases is complex and far from being understood. Unlike the case of cancer, in which genes and mutations that cause the disease were identified, the trigger and the etiology of chronic inflammation is unknown. However, several biochemical pathways are abnormally overactive in most inflammatory diseases and serve as prime suspects for causing the disease.

Such critical pathways are those of the p38 stress/MAP kinase and the ERK MAP kinase. Yet, although considered a target for therapy and is strongly associated with inflammation, the exact role of p38 and ERK in inflammation is not known. It is not even known if their activation would be sufficient to impose inflammation in cells, animals or humans. Such experiments cannot be performed because it is not known how to activate p38 individually in cells or animals. My group is focusing on engineering p38 and other MAP kinases to render them intrinsically active. Using specifically designed Molecular Evolution approaches we were able to isolate intrinsically active variants of p38 and ERK. When these engineered molecules are expressed in biological systems, they are spontaneously active, namely, without the need to expose the system to any stimulation. Thus, only the transgenic molecule is active disclosing most accurately the very specific functions of p38. Using transgenic cells and mice expressing these molecules we shall now be able to answer the question of the linkage between p38, ERK and inflammatory diseases.

Project: MAPK p38α on the inflammatory process

Selected Publications

Engelberg, D., Klein, C., Martinetto, H., Struhl, K. and Karin, M. 1994. The UV response involving the Ras signaling pathway and AP-1 transcription factors is conserved between yeast and mammals. Cell 77, 381-390.

Bell, M., Capone, R., Pashtan, I., Levitzki, A. and Engelberg, D. (2001). Isolation of hyperactive mutants of the MAPK p38/Hog1 that are independent of MAPKK activation. J. Biol. Chem. 276, 25351-25338.

Engelberg, D. 2004. Stress-activated protein kinases – tumor suppressor or tumor initiators? Seminar in Cancer Biology, 14, 271-282

Levin, V., Kogan, K., Ahn, NG., Livnah, O. and Engelberg, D. 2008. Isolation of intrinsically active (MEK-independent) variants of the ERK family of MAP kinases. J. Biol. Chem. 283, 34500-34510.

Smorodinsky-Atias, K., Goshen-Lago, T., Carp, A., Melamed, D., Shir, A., Mooshayef, N., Beenstock, J., Karamansha, Y., Livnah, O., Ahn, N.G., Admon, and Engelberg, D. 2016. Intrinsically active variants of Erk oncogenically transform cells and disclose unexpected autophosphorylation capability that is independent of TEY phosphorylation. Mol.Biol. Cell. 27, 1026-1039.

Beenstock, J., Melamed, D., Mooshayef, N., Mordechay, D., Garfinkel, BP., Ahn, NG., Admon, A., and Engelberg, D (2016). The p38β MAPK Modulates Its Own Basal Activity by Autophosphorylation of the Activating Residue Thr180 and the Inhibitory Residues Thr241 and Ser261. Mol. Cell. Biol. 36, 1540-1554.

Goshen-Lago, T., Goldberg-Carp, A., Melamed, D., Darlyuk-Saadon, I., Ahn, NG., Admon, A., and Engelberg, D. (2016). Variants of the yeast MAPK Mpk1 are biologically functional in a MEK-independent manner, via mechanisms that do not require activation loop phosphorylation. Mol. Biol. Cell. 27, 2771 – 2783.

Beenstock, J., Mooshayf, N. and Engelberg, D. (2016). How kinases take a selfie (autophosphotylate)? An invited review. Trends in Biochemical Sciences (TIBS) 41, 938- 953.

Laboratory Staff

Bai Chen
Snr Research Fellow
micbc@nus.edu.sg

Ilona Saadon
Research Fellow
icis@nus.edu.sg