articlebioRxiv (Cold Spring Harbor Laboratory)Feb 3, 2026GREEN OA

SLC33A1 exports oxidized glutathione to maintain endoplasmic reticulum redox homeostasis

SLShanshan LiuMGMark GadCLCaifan LiKCKevin ChoYLYuyang Liu

Rockefeller University · Memorial Sloan Kettering Cancer Center · +3 more institutions

PubMed
Indexed incrossrefpubmed

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…

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Authors

17
  • SL
    Shanshan Liu

    Rockefeller University

  • MG
    Mark Gad

    Memorial Sloan Kettering Cancer Center, Rockefeller University

  • CL
    Caifan Li

    Rockefeller University

  • KC
    Kevin Cho

    Washington University in St. Louis

  • YL
    Yuyang Liu

    Rockefeller University

Topics & keywords

Keywords
  • Endoplasmic reticulum
  • Homeostasis
  • Redox
  • Glutathione
  • Unfolded protein response
  • Protein disulfide-isomerase
  • Glutathione disulfide
  • Oxidative stress
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