A selective inhibitor of eIF2alpha dephosphorylation protects cells from ER stress.

Article Details

Citation

Boyce M, Bryant KF, Jousse C, Long K, Harding HP, Scheuner D, Kaufman RJ, Ma D, Coen DM, Ron D, Yuan J

A selective inhibitor of eIF2alpha dephosphorylation protects cells from ER stress.

Science. 2005 Feb 11;307(5711):935-9.

PubMed ID
15705855 [ View in PubMed
]
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 broadly, salubrinal demonstrates the feasibility of selective pharmacological targeting of cellular dephosphorylation events.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Serine/threonine-protein phosphatase PP1-gamma catalytic subunitP36873Details
Serine/threonine-protein phosphatase PP1-alpha catalytic subunitP62136Details