4.5 Article

STIM1 gates the store-operated calcium channel ORAI1 in vitro

Journal

NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 17, Issue 1, Pages 112-U137

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.1724

Keywords

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Funding

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NIAID NIH HHS [R01 AI084167, R01 AI084167-07, AI084167, R01 AI040127-20, R01 AI040127, AI40127] Funding Source: Medline
  3. NIDA NIH HHS [RC1 DA028422, RC1 DA028422-02] Funding Source: Medline
  4. NIGMS NIH HHS [GM075256, R01 GM075256] Funding Source: Medline
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI040127, R01AI084167] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM075256] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE ON DRUG ABUSE [RC1DA028422] Funding Source: NIH RePORTER

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Store-operated Ca2+ entry through the plasma membrane Ca2+ release-activated Ca2+ (CRAC) channel in mammalian T cells and mast cells depends on the sensor protein stromal interaction molecule 1 (STIM1) and the channel subunit ORAI1. To study STIM1-ORAI1 signaling in vitro, we have expressed human ORAI1 in a sec6-4 strain of the yeast Saccharomyces cerevisiae and isolated sealed membrane vesicles carrying ORAI1 from the Golgi compartment to the plasma membrane. We show by in vitro Ca2+ flux assays that bacterially expressed recombinant STIM1 opens wild-type ORAI1 channels but not channels assembled from the ORAI1 pore mutant E106Q or the ORAI1 severe combined immunodeficiency (SCID) mutant R91W. These experiments show that the STIM1-ORAI1 interaction is sufficient to gate recombinant human ORAI1 channels in the absence of other proteins of the human ORAI1 channel complex, and they set the stage for further biochemical and biophysical dissection of ORAI1 channel gating.

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