TY - JOUR
T1 - Green fluorescent protein-based lactate and pyruvate indicators suitable for biochemical assays and live cell imaging
AU - Harada, Kazuki
AU - Chihara, Takami
AU - Hayasaka, Yuki
AU - Mita, Marie
AU - Takizawa, Mai
AU - Ishida, Kentaro
AU - Arai, Mary
AU - Tsuno, Saki
AU - Matsumoto, Mitsuharu
AU - Ishihara, Takeshi
AU - Ueda, Hiroshi
AU - Kitaguchi, Tetsuya
AU - Tsuboi, Takashi
N1 - Funding Information:
The authors would like to thank Dr. Daniel Drucker, Dr. Atsushi Miyawaki and Dr. Tomokazu Ito for kindly providing GLUTag cells, Inverse-pericam and D-serine dehydratase plasmids, respectively. The authors also would like to thank Dr. Keitaro Yoshimoto for technical assistance, and Enago (www.enago.jp) for the English language review. This work was supported by Japan Society for the Promotion of Science (JSPS) Grant-in-aid for Scientific Re-search (KAKENHI) (JP16J06838, JP19K23820, and JP20K16118 to K.H., JP18H05135 and JP19H03326 to T.I., JP17K08529, JP20H00575, JP20H04121, JP20H04765, and JP20H04836 to T.T., JP16K01922 and JP18H04832 to T.K.), Kowa Life Science Foundation (to K.H.), The Uehara Memorial Foundation (to K.H.) and Research Foundation for Opto-Science and Technology (to K.H.).
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12
Y1 - 2020/12
N2 - Glycolysis is the metabolic pathway that converts glucose into pyruvate, whereas fermentation can then produce lactate from pyruvate. Here, we developed single fluorescent protein (FP)-based lactate and pyruvate indicators with low EC50 for trace detection of metabolic molecules and live cell imaging and named them “Green Lindoblum” and “Green Pegassos,” respectively. Green Lindoblum (EC50 of 30 µM for lactate) and Green Pegassos (EC50 of 70 µM for pyruvate) produced a 5.2- and 3.3-fold change in fluorescence intensity in response to lactate and pyruvate, respectively. Green Lindoblum measured lactate levels in mouse plasma, and Green Pegassos in combination with D-serine dehydratase successfully estimated D-serine levels released from mouse primary cultured neurons and astrocytes by measuring pyruvate level. Furthermore, live cell imaging analysis revealed their utility for dual-colour imaging, and the interplay between lactate, pyruvate, and Ca2+ in human induced pluripotent stem cell-derived cardiomyocytes. Therefore, Green Lindoblum and Green Pegassos will be useful tools that detect specific molecules in clinical use and monitor the interplay of metabolites and other related molecules in diverse cell types.
AB - Glycolysis is the metabolic pathway that converts glucose into pyruvate, whereas fermentation can then produce lactate from pyruvate. Here, we developed single fluorescent protein (FP)-based lactate and pyruvate indicators with low EC50 for trace detection of metabolic molecules and live cell imaging and named them “Green Lindoblum” and “Green Pegassos,” respectively. Green Lindoblum (EC50 of 30 µM for lactate) and Green Pegassos (EC50 of 70 µM for pyruvate) produced a 5.2- and 3.3-fold change in fluorescence intensity in response to lactate and pyruvate, respectively. Green Lindoblum measured lactate levels in mouse plasma, and Green Pegassos in combination with D-serine dehydratase successfully estimated D-serine levels released from mouse primary cultured neurons and astrocytes by measuring pyruvate level. Furthermore, live cell imaging analysis revealed their utility for dual-colour imaging, and the interplay between lactate, pyruvate, and Ca2+ in human induced pluripotent stem cell-derived cardiomyocytes. Therefore, Green Lindoblum and Green Pegassos will be useful tools that detect specific molecules in clinical use and monitor the interplay of metabolites and other related molecules in diverse cell types.
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U2 - 10.1038/s41598-020-76440-4
DO - 10.1038/s41598-020-76440-4
M3 - Article
C2 - 33177605
AN - SCOPUS:85095822260
SN - 2045-2322
VL - 10
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 19562
ER -