Abstract:Lactate is an energy substrate and intercellular signaling molecule with multiple bodily functions. Lactate has physiological roles in neurogenesis, axon integrity, memory consolidation, immune response, exercise, adipose tissue lipolysis, etc, and is involved in inflammation, cancer and neurodegeneration. The FRET lactate indicator Laconic has been instrumental in the discovery of mechanisms involved in neurometabolic coupling, and has advanced the understanding of lactate transport, glycolysis and mitochondr… Show more
“…Moreover, the ratiometric signal and high dynamic range of HYlight combined with the large changes in FBP that track with alterations of flux ( 30 ) make this sensor an especially useful tool for monitoring metabolism in live cells. HYlight thus complements existing fluorescent biosensors covering the major glycolytic pathway inputs [glucose ( 31 )], outputs [pyruvate ( 32 ) and lactate ( 33 , 34 )], and cofactors [NAD + :NADH ( 35 ) and ATP:ADP ( 8 )].…”
Cellular metabolism is regulated over space and time to ensure that energy production is efficiently matched with consumption. Fluorescent biosensors are useful tools for studying metabolism as they enable real-time detection of metabolite abundance with single-cell resolution. For monitoring glycolysis, the intermediate fructose 1,6-bisphosphate (FBP) is a particularly informative signal as its concentration is strongly correlated with flux through the whole pathway. Using GFP insertion into the ligand-binding domain of the
Bacillus subtilis
transcriptional regulator CggR, we developed a fluorescent biosensor for FBP termed HYlight. We demonstrate that HYlight can reliably report the real-time dynamics of glycolysis in living cells and tissues, driven by various metabolic or pharmacological perturbations, alone or in combination with other physiologically relevant signals. Using this sensor, we uncovered previously unknown aspects of β-cell glycolytic heterogeneity and dynamics.
“…Moreover, the ratiometric signal and high dynamic range of HYlight combined with the large changes in FBP that track with alterations of flux ( 30 ) make this sensor an especially useful tool for monitoring metabolism in live cells. HYlight thus complements existing fluorescent biosensors covering the major glycolytic pathway inputs [glucose ( 31 )], outputs [pyruvate ( 32 ) and lactate ( 33 , 34 )], and cofactors [NAD + :NADH ( 35 ) and ATP:ADP ( 8 )].…”
Cellular metabolism is regulated over space and time to ensure that energy production is efficiently matched with consumption. Fluorescent biosensors are useful tools for studying metabolism as they enable real-time detection of metabolite abundance with single-cell resolution. For monitoring glycolysis, the intermediate fructose 1,6-bisphosphate (FBP) is a particularly informative signal as its concentration is strongly correlated with flux through the whole pathway. Using GFP insertion into the ligand-binding domain of the
Bacillus subtilis
transcriptional regulator CggR, we developed a fluorescent biosensor for FBP termed HYlight. We demonstrate that HYlight can reliably report the real-time dynamics of glycolysis in living cells and tissues, driven by various metabolic or pharmacological perturbations, alone or in combination with other physiologically relevant signals. Using this sensor, we uncovered previously unknown aspects of β-cell glycolytic heterogeneity and dynamics.
“…We and others have recently reported a variety of genetically encoded biosensors for the measurement and imaging of lactate in tissues. [11][12][13][14][15][16][17][18][19][20][21][22][23][24] Applications of these measurement tools would be complemented by a tool for perturbing lactate concentrations. A molecule that enables the photorelease of lactate (that is, a 'caged' lactate) could be a particularly powerful tool for the spatiotemporal manipulation of lactate concentration in tissues.…”
L-Lactate, once considered a metabolic waste product of glycolysis, is now recognized as a vitally important metabolite and signaling molecule in multiple biological pathways. However, exploring L-lactate's emerging intra- and extra-cellular roles is hindered by a lack of tools to locally perturb L-lactate concentration intracellularly and extracellularly. Photocaged compounds are a powerful way to introduce bioactive molecules with spatial and temporal precision using illumination. Here, we report the development of a photocaged derivative of L- lactate, 4-methoxy-7-nitroindolinyl L-lactate (MNI-L-lac), that releases L-lactate upon UV illumination. We validated MNI-L-lac in cell culture by demonstrating that the photorelease of L-lactate elicits a response from genetically encoded extra- and intracellular L-lactate biosensors. These results indicate that MNI-L-lac may be useful for perturbing the concentration of endogenous L-lactate in order to investigate L-lactate's roles in metabolism and signaling pathways.
“…Relative to FRET-based indicators, single FP-based indicators can typically be engineered to have much larger intensiometric fluorescent responses and are suitable for multiplexed imaging applications. In efforts aimed at realizing these advantages, a number of single FP-based L-lactate biosensors have been engineered in recent years [22][23][24][25][26][27] . These single FP-based biosensors share a general design in which the L-lactate-binding protein is genetically linked to an FP such that the binding protein is located close to the chromophore 28 .…”
Section: Introductionmentioning
confidence: 99%
“…. Other recently reported GFP-based L-lactate biosensors have ∆F/F values of <1, 3.0, 4.2, and 6.0 (refs [22][23][24]26)…”
L-Lactate is a monocarboxylate produced during the process of cellular glycolysis and has long been generally considered a waste product. However, studies in recent decades have provided new perspectives on the physiological roles of L-lactate as a major energy substrate and a signaling molecule. To enable further investigations of the physiological roles of L-lactate, we have developed a series of high-performance (ΔF/F = 15 to 30 in vitro), intensiometric, genetically-encoded green fluorescent protein (GFP)-based intracellular L-lactate biosensors with a range of affinities. We evaluated the performance of these biosensors by in vitro and live-cell characterization and demonstrated the utility with imaging applications in several cell lines.
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