TY - JOUR
T1 - A protein-coupled fluorescent probe for organelle-specific imaging of Na+
AU - Taguchi, Ryo
AU - Terai, Takuya
AU - Ueno, Tasuku
AU - Komatsu, Toru
AU - Hanaoka, Kenjiro
AU - Urano, Yasuteru
N1 - Funding Information:
We thank Dr. Tomoya Hirata and Dr. Manabu Shimonishi for helping construction of plasmids. This work was in part supported by the Ministry of Education, Culture, Sports, Science, and Technology of Japan ( 15K05529 and 16J01710 to T.T., 16H06574 to T.U., 16H00823 and 16H05099 to K.H.). T.T. was also supported by Uehara Memorial Foundation and by JSPS fellowship .
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/7/15
Y1 - 2018/7/15
N2 - Intracellular sodium concentration plays important roles in many cellular processes, but methods to analyze dynamic change of [Na+] in organelles of interest are still lacking. To address this problem, controlled localization of fluorescent Na+ probes is a key issue. In this work, we developed a protein-coupled Na+-sensitive fluorescent probe, HaloNa-1, which covalently labelled a HaloTag protein expressed at specific organelles in living cells. Fluorescence intensity of HaloNa-1 increased by approximately three-fold when complexed with Na+, and the dissociation constant was within physiological range. Notably, by conjugating a fluorescent protein to the HaloTag protein and using it as internal standard, one can reduce unwanted variation of probe fluorescence due to different cell volume, HaloTag expression level, etc. With this technique, we could observe elevation of intracellular [Na+] after ionophore stimulation with higher reliability than conventional sensors. We believe our probe is potentially useful to understand Na+ dynamics inside cells.
AB - Intracellular sodium concentration plays important roles in many cellular processes, but methods to analyze dynamic change of [Na+] in organelles of interest are still lacking. To address this problem, controlled localization of fluorescent Na+ probes is a key issue. In this work, we developed a protein-coupled Na+-sensitive fluorescent probe, HaloNa-1, which covalently labelled a HaloTag protein expressed at specific organelles in living cells. Fluorescence intensity of HaloNa-1 increased by approximately three-fold when complexed with Na+, and the dissociation constant was within physiological range. Notably, by conjugating a fluorescent protein to the HaloTag protein and using it as internal standard, one can reduce unwanted variation of probe fluorescence due to different cell volume, HaloTag expression level, etc. With this technique, we could observe elevation of intracellular [Na+] after ionophore stimulation with higher reliability than conventional sensors. We believe our probe is potentially useful to understand Na+ dynamics inside cells.
KW - Cell imaging
KW - Fluorescence probe
KW - HaloTag
KW - Protein labeling
KW - Sodium ion
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U2 - 10.1016/j.snb.2018.03.090
DO - 10.1016/j.snb.2018.03.090
M3 - Article
AN - SCOPUS:85044145747
SN - 0925-4005
VL - 265
SP - 575
EP - 581
JO - Sensors and Actuators, B: Chemical
JF - Sensors and Actuators, B: Chemical
ER -