Zinc regulates ERp44-dependent protein quality control in the early secretory pathway.

Zinc ions (Zn²⁺) are imported into the early secretory pathway by Golgi-resident transporters, but their handling and functions are not fully understood. Here, we show that Zn²⁺ binds with high affinity to the pH-sensitive chaperone ERp44, modulating its localization and ability to retrieve clients like Ero1α and ERAP1 to the endoplasmic reticulum (ER). Silencing the Zn²⁺ transporters that uptake Zn²⁺ into the Golgi led to ERp44 dysfunction and increased secretion of Ero1α and ERAP1. High-resolution crystal structures of Zn²⁺-bound ERp44 reveal that Zn²⁺ binds to a conserved histidine-cluster. The consequent large displacements of the regulatory C-terminal tail expose the substrate-binding surface and RDEL motif, ensuring client capture and retrieval. ERp44 also forms Zn²⁺-bridged homodimers, which dissociate upon client binding. Histidine mutations in the Zn²⁺-binding sites compromise ERp44 activity and localization. Our findings reveal a role of Zn²⁺ as a key regulator of protein quality control at the ER-Golgi interface.

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