It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
l-Lactate, traditionally considered a metabolic waste product, is increasingly recognized as an important intercellular energy currency in mammals. To enable investigations of the emerging roles of intercellular shuttling of l-lactate, we now report an intensiometric green fluorescent genetically encoded biosensor for extracellular l-lactate. This biosensor, designated eLACCO1.1, enables cellular resolution imaging of extracellular l-lactate in cultured mammalian cells and brain tissue.
l-lactate is an important intercellular energy currency. Here the authors report a genetically encoded biosensor eLACCO1.1 to monitor extracellular l-lactate; they use eLACCO1.1 to image extracellular l-lactate in cultured mammalian cells and brain tissue.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details









1 The University of Tokyo, Bunkyo-ku, Department of Chemistry, School of Science, Tokyo, Japan (GRID:grid.26999.3d) (ISNI:0000 0001 2151 536X)
2 Hotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada (GRID:grid.22072.35) (ISNI:0000 0004 1936 7697); Centre Hospitalier de l’Université de Montréal, Department of Neuroscience, Faculty of Medicine, University of Montreal, Montreal, Canada (GRID:grid.410559.c) (ISNI:0000 0001 0743 2111)
3 University of Alberta, Department of Biochemistry, Edmonton, Canada (GRID:grid.17089.37); The First Affiliated Hospital, Xi’an Jiaotong University, Department of Talent Highland, Xi’an, China (GRID:grid.452438.c) (ISNI:0000 0004 1760 8119)
4 Hotchkiss Brain Institute, Cumming School of Medicine, Department of Physiology and Pharmacology, University of Calgary, Calgary, Canada (GRID:grid.22072.35) (ISNI:0000 0004 1936 7697)
5 Montana State University, Department of Microbiology and Cell Biology, Bozeman, USA (GRID:grid.41891.35) (ISNI:0000 0001 2156 6108)
6 Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, USA (GRID:grid.443970.d)
7 University of Alberta, Department of Chemistry, Edmonton, Canada (GRID:grid.17089.37)
8 CERVO Brain Research Center, Laval University, Québec, Canada (GRID:grid.23856.3a) (ISNI:0000 0004 1936 8390); Microbiology and Bioinformatics, Laval University, Department of Biochemistry, Québec, Canada (GRID:grid.23856.3a) (ISNI:0000 0004 1936 8390)
9 University of Alberta, Department of Biochemistry, Edmonton, Canada (GRID:grid.17089.37)
10 The University of Tokyo, Bunkyo-ku, Department of Chemistry, School of Science, Tokyo, Japan (GRID:grid.26999.3d) (ISNI:0000 0001 2151 536X); University of Alberta, Department of Chemistry, Edmonton, Canada (GRID:grid.17089.37)