A Selective Inhibitor of eIF2α Dephosphorylation Protects Cells from ER Stress

Author:

Boyce Michael12345,Bryant Kevin F.12345,Jousse Céline12345,Long Kai12345,Harding Heather P.12345,Scheuner Donalyn12345,Kaufman Randal J.12345,Ma Dawei12345,Coen Donald M.12345,Ron David12345,Yuan Junying12345

Affiliation:

1. Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

2. Department of Biological Chemistry and Molecular Pharmacology and Committee on Virology, Harvard Medical School, Boston, MA 02115, USA.

3. Skirball Institute, New York University School of Medicine, New York, NY 10016, USA.

4. Shanghai Institute of Organic Chemistry, Shanghai, China.

5. Department of Biological Chemistry and Howard Hughes Medical Institute, University of Michigan Medical Center, Ann Arbor, MI 48109, USA.

Abstract

Most protein phosphatases have little intrinsic substrate specificity, making selective pharmacological inhibition of specific dephosphorylation reactions a challenging problem. In a screen for small molecules that protect cells from endoplasmic reticulum (ER) stress, we identified salubrinal, a selective inhibitor of cellular complexes that dephosphorylate eukaryotic translation initiation factor 2 subunit α (eIF2α). Salubrinal also blocks eIF2α dephosphorylation mediated by a herpes simplex virus protein and inhibits viral replication. These results suggest that selective chemical inhibitors of eIF2α dephosphorylation may be useful in diseases involving ER stress or viral infection. More broadly, salubrinal demonstrates the feasibility of selective pharmacological targeting of cellular dephosphorylation events.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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