SLC33A1 exports oxidized glutathione to maintain endoplasmic reticulum redox homeostasis
Rockefeller University · Memorial Sloan Kettering Cancer Center · +3 more institutions
Abstract
The endoplasmic reticulum (ER) requires an oxidative environment to support the efficient maturation of secretory and membrane proteins. This is in part established by glutathione, a redox-active metabolite present in reduced (GSH) and oxidized (GSSG) forms. The ER maintains a higher GSSG:GSH ratio than the cytosol; however, the mechanisms controlling ER redox balance remain poorly understood. To address this, we developed a method for the rapid immunopurification of the ER, enabling comprehensive profiling of its proteome and metabolome. Combining this approach with CRISPR screening, we identified SLC33A1 as the major ER GSSG exporter in mammalian cells. Loss of SLC33A1 leads to GSSG accumulation in the ER…
Citation impact
- FWCI
- 44.72
- Percentile
- 99%
- References
- 78
Authors
17- SLShanshan Liu
Rockefeller University
- MGMark Gad
Memorial Sloan Kettering Cancer Center, Rockefeller University
- CLCaifan Li
Rockefeller University
- KCKevin Cho
Washington University in St. Louis
- YLYuyang Liu
Rockefeller University
Topics & keywords
- Endoplasmic reticulum
- Homeostasis
- Redox
- Glutathione
- Unfolded protein response
- Protein disulfide-isomerase
- Glutathione disulfide
- Oxidative stress