TY - JOUR
T1 - Subcellular metal imaging identifies dynamic sites of Cu accumulation in Chlamydomonas
AU - Hong-Hermesdorf, Anne
AU - Miethke, Marcus
AU - Gallaher, Sean D.
AU - Kropat, Janette
AU - Dodani, Sheel C.
AU - Chan, Jefferson
AU - Barupala, Dulmini
AU - Domaille, Dylan W.
AU - Shirasaki, Dyna I.
AU - Loo, Joseph A.
AU - Weber, Peter K.
AU - Pett-Ridge, Jennifer
AU - Stemmler, Timothy L.
AU - Chang, Christopher J.
AU - Merchant, Sabeeha S.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - 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.
AB - 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.
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U2 - 10.1038/nchembio.1662
DO - 10.1038/nchembio.1662
M3 - Article
C2 - 25344811
AN - SCOPUS:84922481706
SN - 1552-4450
VL - 10
SP - 1034
EP - 1042
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 12
ER -