eIF2B-catalyzed nucleotide exchange and phosphoregulation by the integrated stress response

Lillian R. Kenner(University of California, San Francisco), Aditya Anand(Howard Hughes Medical Institute), Henry C. Nguyen(University of California, San Francisco), Alexander Myasnikov(Centre National de la Recherche Scientifique), Carolin J. Klose(Howard Hughes Medical Institute), Lea A. McGeever(Howard Hughes Medical Institute), Jordan C. Tsai(Howard Hughes Medical Institute), Lakshmi E. Miller-Vedam(University of California, San Francisco), Peter Walter(Howard Hughes Medical Institute), Adam Frost(University of California, San Francisco)
Science
May 2, 2019
Cited by 137Open Access
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Abstract

Integrated stress response on the brain During translation, regulation of protein synthesis by phosphorylation of eukaryotic translation initiation factor 2 (eIF2) is a common consequence of diverse stress stimuli, which leads to reprogramming of gene expression. This process, known as the integrated stress response, is one of the most fundamental mechanisms of translational control conserved throughout eukaryotes. It is also a promising therapeutic target in neurodegenerative diseases and traumatic brain injury. Kashiwagi et al. report the cryo–electron microscopy and crystal structures and Kenner et al. report the cryo–electron microscopy structure of the guanine nucleotide exchange factor eIF2B in complex with eIF2 or phosphorylated eIF2. The structures of the eIF2•eIF2B complex reveal that the single phosphorylation modification on eIF2 changes how eIF2 binds to eIF2B and locks this enzyme into an inhibited complex. Science , this issue p. 495 , p. 491


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