Eukaryotic translation initiation factor, eIF2B, is a guanine nucleotide exchange factor (GEF) composed of five dissimilar subunits. eIF2B is important for regenerating GTP-bound eIF2 during the initiation process. This event is obligatory for eIF2 to bind initiator methionyl-tRNA, forming the ternary initiation complex. In the current investigation, deletion mutants of the catalytic subunit, eIF2Bε, were constructed to identify regions that are necessary for eIF2B catalytic activity and formation of the holoprotein. We used the baculovirus expression system to coexpress wild-type and truncated forms of the ε-subunit of mammalian eIF2B (eIF2Bε) with the other four subunits (α, β, γ, δ) of the protein in Sf9 cells. Removal of either the N- or the C-terminal conserved domains of eIF2Bε resulted in a significant loss of GEF activity and reduced or abolished interaction with the α-, γ- and δ-subunits of eIF2B. Removal of the C-terminal 552 amino acids of eIF2Bε markedly reduced its interaction with the β-subunit of eIF2 whereas loss of the N-terminal 431 amino acids did not. The results suggest that intact eIF2Bε is required for full catalytic activity and formation of the eIF2B holoprotein. In contrast, the C-terminal domain of eIF2Bε is sufficient alone for binding the β-subunit of its substrate, eIF2, in vitro. Copyright (C) 2000 Elsevier Science B.V.
|Original language||English (US)|
|Number of pages||7|
|Journal||Biochimica et Biophysica Acta - Gene Structure and Expression|
|State||Published - Jun 21 2000|
All Science Journal Classification (ASJC) codes
- Structural Biology