- Hong-Hermesdorf, Anne;
- Miethke, Marcus;
- Gallaher, Sean D;
- Kropat, Janette;
- Dodani, Sheel C;
- Chan, Jefferson;
- Barupala, Dulmini;
- Domaille, Dylan W;
- Shirasaki, Dyna I;
- Loo, Joseph A;
- Weber, Peter K;
- Pett-Ridge, Jennifer;
- Stemmler, Timothy L;
- Chang, Christopher J;
- Merchant, Sabeeha S
We identified a Cu-accumulating structure with a dynamic role in intracellular Cu homeostasis. During Zn limitation, Chlamydomonas reinhardtii hyperaccumulates Cu, a process dependent on the nutritional Cu sensor CRR1, but it is functionally Cu deficient. Visualization of intracellular Cu revealed major Cu accumulation sites coincident with electron-dense structures that stained positive for low pH and polyphosphate, suggesting that they are lysosome-related organelles. Nano-secondary ion MS showed colocalization of Ca and Cu, and X-ray absorption spectroscopy was consistent with Cu(+) accumulation in an ordered structure. Zn resupply restored Cu homeostasis concomitant with reduced abundance of these structures. Cu isotope labeling demonstrated that sequestered Cu(+) became bioavailable for the synthesis of plastocyanin, and transcriptome profiling indicated that mobilized Cu became visible to CRR1. Cu trafficking to intracellular accumulation sites may be a strategy for preventing protein mismetallation during Zn deficiency and enabling efficient cuproprotein metallation or remetallation upon Zn resupply.