A Selective Inhibitor of eIF2α Dephosphorylation Protects Cells from ER Stress
Howard Hughes Medical Institute · Harvard University · +2 more institutions
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 alpha (eIF2alpha). Salubrinal also blocks eIF2alpha dephosphorylation mediated by a herpes simplex virus protein and inhibits viral replication. These results suggest that selective chemical inhibitors of eIF2alpha dephosphorylation may be useful in diseases involving ER stress or viral infection. More…
Citation impact
- FWCI
- 20.53
- Percentile
- 100%
- References
- 27
Authors
11- MBMichael Boyce
Howard Hughes Medical Institute, Harvard University, Shanghai Institute of Organic Chemistry, New York University
- KFKevin F. BryantCorresponding
Howard Hughes Medical Institute, Harvard University, Shanghai Institute of Organic Chemistry, New York University
- CJCéline JousseCorresponding
Howard Hughes Medical Institute, Harvard University, Shanghai Institute of Organic Chemistry, New York University
- KLKai LongCorresponding
Howard Hughes Medical Institute, Harvard University, Shanghai Institute of Organic Chemistry, New York University
- HPHeather P. Harding
Howard Hughes Medical Institute, Harvard University, Shanghai Institute of Organic Chemistry, New York University
Topics & keywords
- Dephosphorylation
- Endoplasmic reticulum
- Cell biology
- Phosphatase
- Unfolded protein response
- Phosphorylation
- Chemistry
- Protein subunit
- Good health and well-being