High Sensitivity Detection of Montana Molecular’s Genetically Encoded Sensors Using CLARIOstar®

Introduction

Genetically encoded, fluorescent biosensor-based live cell assays are advantageous in many ways over end point assays in cell lysates. They are able to monitor functional data about the location and timing of cellular responses in cells that are connected to diseases. Fluorescent biosensors, which have been used as basic research tools, have now been improved to facilitate detection on automated plate readers.1

In an earlier study, a live cell cADDIS assay from Montana Molecular for cAMP was employed to demonstrate the production of high Z’ values, characteristic of a robust screening assay2, using the CLARIOstar® microplate reader.

This article discusses the approach of detecting second messengers that are related to the Gq signaling pathway in live cells, using assays for PIP2, diacylglycerol (DAG), and Ca2+.

Here, the integration of spectrally distinct sensors into a single assay is shown to help detect two responses simultaneously. Using the CLARIOstar® in combination with a LVF monochromator or filters enables sensitive detection of such responses.

Assay principle

Packaging the biosensor within a modified baculovirus (BacMam) enables Montana Molecular’s biosensors to show optimal expression in mammalian cells. The mechanism of the DAG sensor is schematically represented in Figure 1, which shows the insertion of a circularly permuted fluorescent protein close to the DAG binding domain of protein kinase C. PIP2 and Ca2+ are detected using similar sensors.

Figure 1. Schematic of DAG sensor. Upon binding DAG, the sensor undergoes conformational changes that lead to changes in fluorescence intensity of the engineered sensor.

Each sensor is available in either a green or red version with the ability to be spectrally resolved. It is possible to detect the changes in two second messengers simultaneously by integrating green or red sensors into a single transduction step.

The two versions of DAG biosensors are Upward DAG (increasing in fluorescence) and Downward DAG (decreasing in fluorescence) and both of them show diacylglycerol increase in live cells.

Gq detection using DAG, PIP2, and Ca2+ sensors

An array of biosensors have been developed by Montana Molecular to unambiguously detect Gq signaling.3,4 hM1R mediated Gq signaling in response to Carbachol is shown in Figure 2. Here, the CLARIOstar® microplate reader was used to validate sensors for DAG, PIP2, and Ca2+.

Figure 2. Signaling from a Gq coupled receptor to PLC after Carbachol stimulation leading to production of PIP2 and subsequently DAG production and Ca2+ mobilization.

Materials and methods

  • Montana Molecular DAG sensors, PIP2 sensors, R-GECO Ca2+ sensors packaged in BacMam
  • HEK293 cells
  • CLARIOstar® microplate reader from BMG LABTECH
  • Greiner 96-well F bottom plates

Transduction of the indicated sensor packaged in BacMam was carried out on HEK293 cells in suspension. After subsequently plating the cells in 96-well microplates, sensor expression was carried out for 24 to 36 hours. 30 minutes before the experiment, media was replaced with PBS and cells were kept undisturbed at room temperature.

Instrument settings

Detection Mode

FI (well mode), bottom optic

Number of flashes

5

Scan mode

Orbital

Scan diameter (mm)

2

Gain / Focal height

Adjusted prior to test run

Interval time

3-11 seconds

Optical settings

Green

Red

Excitation

F 482-16

560-15

Dichroic

LP 504

auto580.5

Emission

F 530-40

618-49

Injection settings

Volume (μl)

50

Pump speed (μl/s)

85

Injection start time (s)

30

Results and discussion

Figure 3 presents the experimental results, showing the brilliant assay performance exhibited by the DAG sensor.

Figure 3. DAG assay performance. Comparison of 14 replicates treated with Carbachol (white) or vehicle [PBS] (purple) indicates robust assay performance. Z’ = 0.8.

The results of a multiplexed experiment in response to Carbachol are shown in Figure 4, indicating the very rapid release of calcium and rapid DAG production following injection of the compound.

Figure 4. Multiplexed DAG and Ca2+ kinetics. Traces depict the average response to 30 µM Carbachol (n=16) expressed as 100% response. R-GECO (red); green DAG (green). Carbachol was dispensed using on-board reagent injectors at the 30 second time point as indicated.

The results of another multiplexed experiment are shown in Figure 5, where a sensor for PIP2 and the Downward DAG sensor were used.

Figure 5. Multiplexed DAG and PIP2 kinetics. Traces depict average response to 30 µM Carbachol (n=18). Red DAG (red), green PIP2 (green). On board reagent injectors dispensed 50 µl of Carbachol after 30 seconds as indicated.

Conclusion

The CLARIOstar® facilitates high sensitivity detection of Montana Molecular’s genetically encoded sensors. Spectrally resolved variants show simultaneous changes in several second messengers subsequent to Gq activation.

Acknowledgements

Produced from materials originally authored by P. Tewson1, S. Martinka1 , S. Tillo1 , T. Hughes1 , A.M. Quinn1 , C. Peters2 from:

1 Montana Molecular, Bozeman, MT

2 BMG LABTECH, Cary, NC

References

  1. Tewson, P., et al (2016) J. Biomol. Screen. 21:298-305
  2. Tewson, P., et al (2016) Real-Time Detection of Gs and Gi Signalling in Living Cells
  3. Ding, Y., et al (2015) Nature Methods 12:195-198
  4. Tewson, P., et al (2012) Simultaneous Detection of Ca2+ and Diacylglycerol Signaling in Living Cells

About BMG Labtech

BMG LABTECH GmbH,BMG LABTECH is a leading developer and global manufacturer of microplate reader instrumentation with a wide range of measurement methods. Microplate readers are used in the pharmaceutical and biotech industries, as well as in academic research establishments, for both basic research analysis and High Throughput Screening. BMG LABTECH focuses solely on microplate readers and offers the most diverse selection of optical detection systems in conjunction with integrated liquid handling equipment.


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Last updated: Apr 10, 2017 at 7:33 AM

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