A structure of human Scap bound to Insig-2 suggests how their interaction is regulated by sterols

A cellular cholesterol sensor Cholesterol levels in cells are controlled by the sterol regulatory element–binding protein (SREBP) pathway. When the cell has sufficient cholesterol, the transcription factor that regulates cholesterol metabolism is sequestered at the endoplasmic reticulum membrane, but when cholesterol is depleted, the transcription factor is released to activate the expression of genes involved in cholesterol synthesis and uptake. Yan et al. determined the structure of a central complex in human SREBP containing the proteins Scap and Insig-2. These two membrane-embedded proteins undergo 25-hydroxycholesterol (25HC)–dependent association and must dissociate for the pathway to be activated. The structure shows that 25HC is sandwiched between Scap and Insig-2 to facilitate their association. A mutational analysis is consistent with the structural model. Science , this issue p. eabb2224