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Method Article

LED Thermo Flow — Combining Optogenetics with Flow Cytometry

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DOI:

10.3791/54707

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December 30th, 2016

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In This Article

Summary

Optically controlled substances are powerful tools to study signaling pathways. To expand the spectrum of possible experiments, we developed a device for studying optically controlled substances in real time using flow cytometry: the LED Thermo Flow.

Abstract

Optogenetic tools allow isolated, functional investigations of almost any signaling molecule within complex signaling pathways. A major obstacle is the controlled delivery of light to the cell sample and hence the most popular tools for optogenetic studies are microscopy-based cell analyses and in vitro experiments. The flow cytometer has major advantages over a microscope, including the ability to rapidly measure thousands of cells at single cell resolution. However, it is not yet widely used in optogenetics. Here, we present a device that combines the power of optogenetics and flow cytometry: the LED Thermo Flow. This device illuminates cells at specific wavelengths, light intensities and temperatures during flow cytometric measurements. It can be built at low cost and be used with most common flow cytometers. To demonstrate its utility, we characterized the photoswitching kinetics of Dronpa proteins in vivo and in real time. This protocol can be adapted to almost all optically controlled substances and substantially expands the set of possible experiments. More importantly, it will greatly simplify the discovery and development of new optogenetic tools.

Introduction

Optogenetic tools have been gaining popularity, in part because they can be used to decipher the wiring of signaling pathways1-4. They are based on the ability of photoactivatable proteins to change their conformation and binding affinity when illuminated with light. Fusing these proteins to signaling elements allows for the specific regulation of a single player within complex intracellular signaling pathways5-12. Consequently, a signaling pathway can be studied with high temporal and spatial resolution.

Most cell-based optogenetic studies utilize microscopy-based methods combined with culturing in the presence of lig....

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Protocol

1. Designing and Building the Device

  1. Pilot Experiments
    NOTE: The required light intensity for a specific optogenetic tool and cell type may vary significantly. Pilot experiments with prototypes are useful to estimate the minimal light intensity necessary. The optogenetic tool used for the following experiments is a Dronpa-Linker-Dronpa fusion construct. The Dronpa sequence was commercially obtained (See List of Materials). A long linker was cloned in between two Dronpa sequences to allow the expressed construct to form intramolecular (and intermolecular) dimers. The steps described below can be adapted to many other optogenetic tool....

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Results

Using the LED Thermo Flow with a Flow Cytometer

The functional core of the device is a cylindrical chamber in which LED lights are arranged in a circular manner pointing inward. This chamber can be connected to a water supply and pump, which allows for controlling the temperature of the LEDs, as well as the cell sample. The LEDs are connected to a transformer and hence the light intensity for each wavelength can be individually co.......

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Discussion

The LED Thermo Flow is an innovative device to study optogenetic tools in a flow cytometer.

So far, optogenetic samples have been illuminated only with microscopy lasers or flashlight devices11,12. Depending on the angle and distance of the flashlight to the sample, substantial variability in the amount of illumination is expected between experiments. Furthermore, there is a limit to the number of flashlights a single person can operate in an experiment. This restricts the experimen.......

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Disclosures

The authors declare that they have no competing financial interests.

Acknowledgements

We thank J. Schmidt from the University of Freiburg for constructing the device. We thank P. Nielsen and D. Medgyesi for their support and critical reading of this manuscript. This study was supported by the Deutsche Forschungsgemeinschaft through SFB746 and by the Excellence Initiative of the German Research Foundation (GSC-4, Spemann Graduate School).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Glass FACS tubeThermo Fisher Scientific; Waltham, USA14-961-26Borosilicate glass tubes 12x75 mm
Flow CytometerBD Bioscienceg; Heidelberg, GermanyFortessa IISpecial Order
Dronpa: pcDNA3-mNeptune2-NAddgene; Cambridge, USA41645
PolyJetSignaGen, Rockville, USASL100688
LED 505 nmAvago Technologies; Boeblingen, GermanyHLMP-CE34-Y1CDD
LED 400 nmAvago Technologies; Boeblingen, GermanyUV5TZ-400-15
Plexiglas tube 15 mmMaertin; Freiburg, Germany76999
Plexiglas 3 mmMaertin; Freiburg, Germany692230
Plexiglas 2.5 mmMaertin; Freiburg, Germany692225
Plexiglas 1.5 mmMaertin; Freiburg, Germany692215
PVC tile 5 mmMaertin; Freiburg, Germany690020.005
PVC tile 6 mmMaertin; Freiburg, Germany690020.006
PVC block 50 mmMaertin; Freiburg, Germany690020.050
RPMIInvitrogen, Life Technologies; Darmstadt, Germany61870-010
2-MercaptoethanolEMD; Germany805740
FCSPAN Biotech; Aidenbach, GermanyP30-3302
Penicillin/Strptomycin (10,000 U/mL)Invitrogen, Life Technologies; Darmstadt, Germany15140-122
Acrifix plexiglas glueEvonic industries, Essen, Germany1R0192
Tangit PVC-U glueHenkel, Düsseldorf, Germany

References

  1. Dugue, G. P., Akemann, W., Knopfel, T. A comprehensive concept of optogenetics. Prog Brain Res. 196, 1-28 (2012).
  2. Tischer, D., Weiner, O. D. Illuminating cell signalling with optogenetic tools. Nat Rev Mol Cell Biol. 15 (8), 551-558 (2014).
  3. Toettcher, J. E., Voigt, C. A., Wein....

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