
Neuron, Год журнала: 2016, Номер 90(3), С. 471 - 482
Опубликована: Май 1, 2016
Язык: Английский
Neuron, Год журнала: 2016, Номер 90(3), С. 471 - 482
Опубликована: Май 1, 2016
Язык: Английский
Nature reviews. Neuroscience, Год журнала: 2017, Номер 18(4), С. 222 - 235
Опубликована: Март 17, 2017
Язык: Английский
Процитировано
648Nature Neuroscience, Год журнала: 2016, Номер 19(9), С. 1142 - 1153
Опубликована: Авг. 26, 2016
Язык: Английский
Процитировано
620Trends in Biochemical Sciences, Год журнала: 2016, Номер 42(2), С. 111 - 129
Опубликована: Ноя. 1, 2016
Язык: Английский
Процитировано
576Science, Год журнала: 2015, Номер 350(6266), С. 1361 - 1366
Опубликована: Дек. 11, 2015
In vivo imaging of neuronal voltage spikes Neuroscientists have long sought tools that allow optical individual neurons' membrane dynamics in awake behaving animals. Gong et al. genetically engineered a protein indicator can report action potentials with <1-ms precision and orders magnitude lower spike detection error rates than were previously possible. They thus able to record the brains mice fruit flies. Science , this issue p. 1361
Язык: Английский
Процитировано
460Science, Год журнала: 2015, Номер 347(6223), С. 755 - 760
Опубликована: Фев. 12, 2015
The identification of active neurons and circuits in vivo is a fundamental challenge understanding the neural basis behavior. Genetically encoded calcium (Ca(2+)) indicators (GECIs) enable quantitative monitoring cellular-resolution activity during However, such require online within limited field view. Alternatively, post hoc staining immediate early genes (IEGs) indicates highly cells entire brain, albeit with poor temporal resolution. We designed fluorescent sensor, CaMPARI, that combines genetic targetability link to GECIs permanent, large-scale labeling IEGs, allowing temporally precise "activity snapshot" large tissue volume. CaMPARI undergoes efficient irreversible green-to-red conversion only when elevated intracellular Ca(2+) experimenter-controlled illumination coincide. demonstrate utility freely moving larvae zebrafish flies, head-fixed mice adult flies.
Язык: Английский
Процитировано
447Chemical Reviews, Год журнала: 2018, Номер 118(24), С. 11707 - 11794
Опубликована: Дек. 14, 2018
Cellular signaling networks are the foundation which determines fate and function of cells as they respond to various cues stimuli. The discovery fluorescent proteins over 25 years ago enabled development a diverse array genetically encodable biosensors that capable measuring spatiotemporal dynamics signal transduction pathways in live cells. In an effort encapsulate breadth have expanded, we endeavored assemble comprehensive list published engineered biosensors, discuss many molecular designs utilized their development. Then, review how high temporal spatial resolution afforded by has aided our understanding regulation at cellular subcellular level. Finally, highlight some emerging areas research both biosensor design applications on forefront
Язык: Английский
Процитировано
445Science, Год журнала: 2019, Номер 365(6454), С. 699 - 704
Опубликована: Авг. 1, 2019
Genetically encoded voltage indicators (GEVIs) enable monitoring of neuronal activity at high spatial and temporal resolution. However, the utility existing GEVIs has been limited by brightness photostability fluorescent proteins rhodopsins. We engineered a GEVI, called Voltron, that uses bright photostable synthetic dyes instead protein-based fluorophores, thereby extending number neurons imaged simultaneously in vivo factor 10 enabling imaging for significantly longer durations relative to GEVIs. used Voltron mice, zebrafish, fruit flies. In mouse cortex, allowed single-trial recording spikes subthreshold signals from dozens over 15-minute period continuous imaging. larval enabled precise correlation spike timing with behavior.
Язык: Английский
Процитировано
444Science Advances, Год журнала: 2017, Номер 3(6)
Опубликована: Июнь 2, 2017
Multimodal and multidisciplinary approaches lead to next-generation technologies for reading modulating neural function.
Язык: Английский
Процитировано
438Sensors, Год журнала: 2016, Номер 16(9), С. 1488 - 1488
Опубликована: Сен. 14, 2016
Förster or fluorescence resonance energy transfer (FRET) technology and genetically encoded FRET biosensors provide a powerful tool for visualizing signaling molecules in live cells with high spatiotemporal resolution. Fluorescent proteins (FPs) are most commonly used as both donor acceptor fluorophores biosensors, especially since FPs encodable live-cell compatible. In this review, we will an overview of methods to measure changes biological contexts, discuss the palette FP pairs developed their relative strengths weaknesses, note important factors consider when using studies.
Язык: Английский
Процитировано
413Nature Methods, Год журнала: 2020, Номер 17(11), С. 1156 - 1166
Опубликована: Окт. 21, 2020
Язык: Английский
Процитировано
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