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A highly efficient human cell-free translation system.
Aleksashin, Nikolay A; Chang, Stacey Tsai-Lan; Cate, Jamie H D.
Affiliation
  • Aleksashin NA; Innovative Genomics Institute, University of California-Berkeley, Berkeley, California 94720, USA.
  • Chang ST; Department of Molecular and Cell Biology, University of California-Berkeley, Berkeley, California 94720, USA.
  • Cate JHD; Innovative Genomics Institute, University of California-Berkeley, Berkeley, California 94720, USA.
RNA ; 29(12): 1960-1972, 2023 12.
Article in En | MEDLINE | ID: mdl-37793791
Cell-free protein synthesis (CFPS) systems enable easy in vitro expression of proteins with many scientific, industrial, and therapeutic applications. Here we present an optimized, highly efficient human cell-free translation system that bypasses many limitations of currently used in vitro systems. This CFPS system is based on extracts from human HEK293T cells engineered to endogenously express GADD34 and K3L proteins, which suppress phosphorylation of translation initiation factor eIF2α. Overexpression of GADD34 and K3L proteins in human cells before cell lysate preparation significantly simplifies lysate preparation. We find that expression of the GADD34 and K3L accessory proteins before cell lysis maintains low levels of phosphorylation of eIF2α in the extracts. During in vitro translation reactions, eIF2α phosphorylation increases moderately in a GCN2-dependent fashion that can be inhibited by GCN2 kinase inhibitors. This new CFPS system should be useful for exploring human translation mechanisms in more physiological conditions outside the cell.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Eukaryotic Initiation Factor-2 Limits: Humans Language: En Journal: RNA Journal subject: BIOLOGIA MOLECULAR Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Proteins / Eukaryotic Initiation Factor-2 Limits: Humans Language: En Journal: RNA Journal subject: BIOLOGIA MOLECULAR Year: 2023 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos