TY - JOUR
T1 - A dual-fluorophore sensor approach for ratiometric fluorescence imaging of potassium in living cells
AU - Wang, Zeming
AU - Detomasi, Tyler C.
AU - Chang, Christopher J.
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2020.
PY - 2021/2/7
Y1 - 2021/2/7
N2 - Potassium is the most abundant intracellular metal in the body, playing vital roles in regulating intracellular fluid volume, nutrient transport, and cell-to-cell communication through nerve and muscle contraction. On the other hand, aberrant alterations in K+homeostasis contribute to a diverse array of diseases spanning cardiovascular and neurological disorders to diabetes to kidney disease to cancer. There is an unmet need for studies of K+physiology and pathology owing to the large differences in intracellularversusextracellular K+concentrations ([K+]intra= 150 mM, [K+]extra= 3-5 mM). With a relative dearth of methods to reliably measure dynamic changes in intracellular K+in biological specimens that meet the dual challenges of low affinity and high selectivity for K+, particularly over Na+, currently available fluorescent K+sensors are largely optimized with high-affinity receptors that are more amenable for extracellular K+detection. We report the design, synthesis, and biological evaluation of Ratiometric Potassium Sensor 1 (RPS-1), a dual-fluorophore sensor that enables ratiometric fluorescence imaging of intracellular potassium in living systems.RPS-1links a potassium-responsive fluorescent sensor fragment (PS525) with a low-affinity, high-selectivity crown ether receptor for K+to a potassium-insensitive reference fluorophore (Coumarin 343) as an internal calibration standard through ester bonds. Upon intracellular delivery, esterase-directed cleavage splits these two dyes into separate fragments to enable ratiometric detection of K+.RPS-1responds to K+in aqueous buffer with high selectivity over competing metal ions and is sensitive to potassium ions at steady-state intracellular levels and can respond to decreases or increases from that basal set point. Moreover,RPS-1was applied for comparative screening of K+pools across a panel of different cancer cell lines, revealing elevations in basal intracellular K+in metastatic breast cancer cell linesvs.normal breast cells. This work provides a unique chemical tool for the study of intracellular potassium dynamics and a starting point for the design of other ratiometric fluorescent sensors based on two-fluorophore approaches that do not rely on FRET or related energy transfer designs.
AB - Potassium is the most abundant intracellular metal in the body, playing vital roles in regulating intracellular fluid volume, nutrient transport, and cell-to-cell communication through nerve and muscle contraction. On the other hand, aberrant alterations in K+homeostasis contribute to a diverse array of diseases spanning cardiovascular and neurological disorders to diabetes to kidney disease to cancer. There is an unmet need for studies of K+physiology and pathology owing to the large differences in intracellularversusextracellular K+concentrations ([K+]intra= 150 mM, [K+]extra= 3-5 mM). With a relative dearth of methods to reliably measure dynamic changes in intracellular K+in biological specimens that meet the dual challenges of low affinity and high selectivity for K+, particularly over Na+, currently available fluorescent K+sensors are largely optimized with high-affinity receptors that are more amenable for extracellular K+detection. We report the design, synthesis, and biological evaluation of Ratiometric Potassium Sensor 1 (RPS-1), a dual-fluorophore sensor that enables ratiometric fluorescence imaging of intracellular potassium in living systems.RPS-1links a potassium-responsive fluorescent sensor fragment (PS525) with a low-affinity, high-selectivity crown ether receptor for K+to a potassium-insensitive reference fluorophore (Coumarin 343) as an internal calibration standard through ester bonds. Upon intracellular delivery, esterase-directed cleavage splits these two dyes into separate fragments to enable ratiometric detection of K+.RPS-1responds to K+in aqueous buffer with high selectivity over competing metal ions and is sensitive to potassium ions at steady-state intracellular levels and can respond to decreases or increases from that basal set point. Moreover,RPS-1was applied for comparative screening of K+pools across a panel of different cancer cell lines, revealing elevations in basal intracellular K+in metastatic breast cancer cell linesvs.normal breast cells. This work provides a unique chemical tool for the study of intracellular potassium dynamics and a starting point for the design of other ratiometric fluorescent sensors based on two-fluorophore approaches that do not rely on FRET or related energy transfer designs.
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U2 - 10.1039/d0sc03844j
DO - 10.1039/d0sc03844j
M3 - Article
C2 - 34163931
AN - SCOPUS:85101165848
SN - 2041-6520
VL - 12
SP - 1720
EP - 1729
JO - Chemical Science
JF - Chemical Science
IS - 5
ER -