TY - JOUR
T1 - A DNA nanodevice for mapping sodium at single-organelle resolution
AU - Zou, Junyi
AU - Mitra, Koushambi
AU - Anees, Palapuravan
AU - Oettinger, Daphne
AU - Ramirez, Joseph R.
AU - Veetil, Aneesh Tazhe
AU - Gupta, Priyanka Dutta
AU - Rao, Rajini
AU - Smith, Jayson J.
AU - Kratsios, Paschalis
AU - Krishnan, Yamuna
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2023.
PY - 2024/7
Y1 - 2024/7
N2 - Cellular sodium ion (Na+) homeostasis is integral to organism physiology. Our current understanding of Na+ homeostasis is largely limited to Na+ transport at the plasma membrane. Organelles may also contribute to Na+ homeostasis; however, the direction of Na+ flow across organelle membranes is unknown because organellar Na+ cannot be imaged. Here we report a pH-independent, organelle-targetable, ratiometric probe that reports lumenal Na+. It is a DNA nanodevice containing a Na+-sensitive fluorophore, a reference dye and an organelle-targeting domain. By measuring Na+ at single endosome resolution in mammalian cells and Caenorhabditiselegans, we discovered that lumenal Na+ levels in each stage of the endolysosomal pathway exceed cytosolic levels and decrease as endosomes mature. Further, we find that lysosomal Na+ levels in nematodes are modulated by the Na+/H+ exchanger NHX-5 in response to salt stress. The ability to image subcellular Na+ will unveil mechanisms of Na+ homeostasis at an increased level of cellular detail.
AB - Cellular sodium ion (Na+) homeostasis is integral to organism physiology. Our current understanding of Na+ homeostasis is largely limited to Na+ transport at the plasma membrane. Organelles may also contribute to Na+ homeostasis; however, the direction of Na+ flow across organelle membranes is unknown because organellar Na+ cannot be imaged. Here we report a pH-independent, organelle-targetable, ratiometric probe that reports lumenal Na+. It is a DNA nanodevice containing a Na+-sensitive fluorophore, a reference dye and an organelle-targeting domain. By measuring Na+ at single endosome resolution in mammalian cells and Caenorhabditiselegans, we discovered that lumenal Na+ levels in each stage of the endolysosomal pathway exceed cytosolic levels and decrease as endosomes mature. Further, we find that lysosomal Na+ levels in nematodes are modulated by the Na+/H+ exchanger NHX-5 in response to salt stress. The ability to image subcellular Na+ will unveil mechanisms of Na+ homeostasis at an increased level of cellular detail.
UR - http://www.scopus.com/inward/record.url?scp=85171652021&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85171652021&partnerID=8YFLogxK
U2 - 10.1038/s41587-023-01950-1
DO - 10.1038/s41587-023-01950-1
M3 - Article
C2 - 37735265
AN - SCOPUS:85171652021
SN - 1087-0156
VL - 42
SP - 1075
EP - 1083
JO - Nature biotechnology
JF - Nature biotechnology
IS - 7
ER -