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Summary

Optical biosensor techniques can detect changes in mass near the plasma membrane in living cells and allow one to follow cellular responses in both individual cells and populations of cells. This protocol will describe detection of the modulation of potassium channels by G-protein coupled receptors in intact cells using this approach.

Abstract

Ion channels control the electrical properties of neurons and other excitable cell types by selectively allowing ions to flow through the plasma membrane¹. To regulate neuronal excitability, the biophysical properties of ion channels are modified by signaling proteins and molecules, which often bind to the channels themselves to form a heteromeric channel complex^2,3. Traditional assays examining the interaction between channels and regulatory proteins require exogenous labels that can potentially alter the protein's behavior and decrease the physiological relevance of the target, while providing little information on the time course of interactions in living cells. Optical biosensors, such as the X-BODY Biosciences BIND Scanner system, use a novel label-free technology, resonance wavelength grating (RWG) optical biosensors, to detect changes in resonant reflected light near the biosensor. This assay allows the detection of the relative change in mass within the bottom portion of living cells adherent to the biosensor surface resulting from ligand induced changes in cell adhesion and spreading, toxicity, proliferation, and changes in protein-protein interactions near the plasma membrane. RWG optical biosensors have been used to detect changes in mass near the plasma membrane of cells following activation of G protein-coupled receptors (GPCRs), receptor tyrosine kinases, and other cell surface receptors. Ligand-induced changes in ion channel-protein interactions can also be studied using this assay. In this paper, we will describe the experimental procedure used to detect the modulation of Slack-B sodium-activated potassium (K_Na) channels by GPCRs.

Introduction

Examining living cells in their physiologically relevant context is crucial to understanding the biological functions of cellular targets. However, assays examining the interaction between channels and regulatory cytoplasmic proteins, such as coimmunoprecipitation assays, generally provide little information on the time course of interactions in living cells. The majority of current cell based assays measure a specific cellular event, such as the translocation of a fluorescently tagged protein of interest. These assays require modifications of the proteins of interest, which can potentially alter the protein's behavior and decrease the physiological relevance of the target. Noninvasive cell based assays, which do not require manipulation of the system, provide a continuous measurement of cellular activity and allow studies of cells in their most physiologically relevant state⁴.

Optical biosensors are designed to produce a measureable change in a characteristic of the light that is coupled to the sensor surface. Optical biosensors that utilize evanescent waves, which include surface plasmon resonance (SPR) and resonance wavelength grating (RWG) techniques, have been primarily used to detect the affinities and kinetics of molecules binding to their biological receptors immobilized on the sensor surface. More recently, commercially available RWG biosensors have been developed to allow the detection of the relative change in mass within the bottom portion of cells adherent to the sensor surface at high spatial resolution (up to 3.75 µm/pixel)⁵. These biosensors can detect changes in mass near the plasma membrane of living cells that result from stimulation, such as cell adhesion and spreading, toxicity, proliferation and signaling pathways elicited by a variety of cell surface receptors including G-protein coupled receptors (GPCRs)⁶. RWG biosensors detect the relative change in the index of refraction as a function of the relative change in mass within 150 nm of the biosensor⁷. When cells are plated to the biosensor, this change in the index of refraction reflects the change in mass near the plasma membrane of the cell resulting from a change in cellular adherence to the biosensor. This protocol will discuss the detection of channel-protein interactions using RWG biosensors.

RWG data acquisition systems consist of several components. Because the X-BODY Biosciences BIND Scanner was used for these experiments, we shall refer to the components for this particular system, which consists of a plate reader, associated biosensors, BIND Scan acquisition software, and BIND View analysis software⁸. The photonic crystal biosensors, referred to hereafter as optical biosensors, are composed of a periodic arrangement of a dielectric and material in 2 or 3 dimensions which prevents the propagation of light at specific wavelengths and directions. Photonic crystal structures are based on a phenomenon called Wood's anomaly. First discovered by Wood in 1902, these anomalies are effects observed in the spectrum of light reflected by optical diffraction gratings where rapid variations in the intensity of particular diffraction orders occur in certain narrow frequency bands. In 1962, Hessel and Oliner presented a new theory of Wood's anomalies in which finite period grating generates a standing resonance wavelength⁹. In the optical biosensors described here, Wood's anomalies are used to produce a RWG biosensor that when stimulated with white light reflects only very narrow band of wavelengths (typically between 850-855 nm).

Individual biosensors consist of a low-refractive index plastic material with a periodic surface structure which is coated with a thin layer of the high-refractive dielectric material titanium dioxide (TiO₂). When the biosensor is illuminated with a broad wavelength light source, the optical grating of photonic crystals reflects a narrow range of wavelengths of light which is measured by a spectrophotometer in the BIND Scanner. The peak intensity of the reflected wavelengths (Peak Wavelength Value, or PWV) is then calculated from the signal. The PWV of light shifts upon a change in the index of refraction as a result of an increase or decrease in mass within the proximity (~150 nm) of the biosensor surface. Optical biosensors are incorporated into a standard Society for Biomolecular Sciences (SBS) 384-well microplate for the assays used in these experiments.

RWV biosensors are used to detect changes upon addition of exogenous signals in living cells¹⁰. Cells are directly cultured onto the surface of a RWG biosensor and the change in the local index of refraction is monitored upon treatment with specific stimuli. The direction of change in mass at the biosensor can be determined, because an increase in the local index of refraction results from an increase in mass near the biosensor and is measured as an increase in PWV. Conversely a decrease in mass produces a decrease in PWV. The change in detected PWV can result from numerous cellular events, including changes in cell adhesion, protein recruitment/release, endocytosis and recycling, exocytosis, apoptosis, and cytoskeletal rearrangement. For example, the assay can be detect changes in channel-protein interactions between potassium channels and other cytoplasmic or cytoskeletal components. The event, however, must occur within the ~150 nm detection zone near the biosensor, and in the case of an attached cell, near the plasma membrane. Acquisition of cellular responses is performed with BIND Scan software and an image representation of each of the 384 wells in the SBS plate is generated. This system has a resolution of up to 3.75 µm/pixel, allowing detection of events in single cells, and can be used either with cell lines (such as HEK293 or CHO cells) or with more physiologically relevant primary cells. Image analysis with BIND View software allows the detection of cellular responses in both individual and populations of cells. As the biosensors are incorporated into standard SBS 384-well microplates, the system is readily adaptable to high-throughput screening (HTS).

Resonance-wavelength grating optical biosensors have previously been used to detect changes in mass near the plasma membrane of cells following activation of GPCRs¹¹. Our laboratory has cloned two sodium-activated (K_Na) potassium channels, Slack-B and Slick¹². The activity of both Slack-B and Slick channels has been shown to be very strongly influenced by direct activation of protein kinase C (PKC)¹³. Activation of Gα_q protein coupled receptors, such as the M1 muscarinic receptor and the mGluR1 metabotropic glutamate receptor, potently regulates channel activity through PKC activation. These K_Na channels contribute to neuronal adaptation during sustained stimulation and regulate the accuracy of timing of action potentials¹⁴. Slack channels are known to interact with a variety of cytoplasmic signaling molecules, including FMRP, the Fragile X Mental Retardation protein^15,16. Mutations in Slack result in Multiple Migrating Partial Seizures of Infancy (MMPSI), an early onset form of epilepsy which results in severe developmental delay¹⁷.

Protocol

1. Cell Culture (Adapted from Fleming and Kaczmarek18) Culture cells in appropriate media for greater than 2 but less than 10 passages before use in this assay. Untransfected HEK-293 cells and HEK-293 cells stably expressing rat Slack-B protein are grown in one half Dulbecco's Modified Eagle medium and one half Leibovitz's L-15 Medium supplemented with 10% heat inactivated fetal bovine serum and antibiotics. 500 µg/ml Geneticin (G418) is added to HEK-293 cells stably expressing Slack-B to select for expression of the Slack channel. Passage cells at 70-90% confluence by dissociation from dishes with a 0.25% trypsin-EDTA solution. 2. Extracellular Matrix (ECM) Coating of the TiO2 384-well Optical Biosensor Plate with Fibronectin and Ovalbumin Preparation of the fibronectin ECM mixture and ovalbumin blocking solution Prepare a working solution of fibronectin in phosphate buffered saline (PBS) with a final concentration of 5 µg/ml of fibronectin in 20.0 ml PBS. From a 1.0 mg/ml stock concentration, add 100 µl to 20.0 ml PBS for a 200-fold dilution. The working solution of fibronectin can be aliquoted and stored at -20 °C after preparation. Prepare a 5% stock solution of heat-inactivated ovalbumin in sterile water. Dilute ovalbumin in sterile tissue culture grade water for a 5% solution and heat-inactivate for 30 min at 60 °C. Cool the solution to room temperature and sterile filter the solution. Aliquot the 5% ovalbumin solution and store at 4 °C. Prepare a 2% working solution of ovalbumin by diluting the 5% stock solution into PBS. For example, add 12.0 ml of 5% ovalbumin stock solution to 18.0 ml of PBS for a final volume of 30.0 ml. 384-well optical biosensor plate coating Hydrate the TiO2 plate with 20.0 µl/well of sterile tissue culture grade water for 15 min. The following steps should be performed with a 16-channel pipettor. Wash plate 1x with 50.0 µl PBS per well. Add 20.0 µl of the fibronectin working solution to each well and incubate for 2 hr at room temperature to create the ECM. Wash plate 1x with 50.0 µl PBS per well. Add 40.0 µl of the ovalbumin working solution to each well and incubate overnight at 4 °C to block the plate. Wash plate 3x with 50.0 µl PBS per well. ECM coated plates can be stored at 4 °C for up to 48 hr. 3. Seeding of Cells onto the 384-well Optical Biosensor Plate Remove growth media from the cells and add trypsin to dislodge the cells from the plate. Collect the cells and centrifuge at 1,000 x g for 1 min. Remove the trypsin media and resuspend cells in growth media. Using a hemocytometer or an automated cell counter, determine the concentration of the cells. To minimize the effects of evaporation during incubation, 50.0 µl of growth medium per well will be used. Cells should be diluted to achieve the desired number of cells per well in a volume of 50.0 µl of growth medium. For these experiments, 1,000 cells/well were plated onto the biosensor. Allow the seeded cells to incubate overnight in growth medium at 37 °C under air/5% CO2. 4. Preparation of the Biosensor and Compound Plates for the RWG Optical Biosensor Assay Remove the plate from the incubator and remove growth media from the cells. Wash the cells 1x with Hanks Balanced Salt Solution (HBSS). Add 25.0 µl of HBSS to each well. Place the biosensor plate on the BIND Scanner and allow the cells to equilibrate to room temperature for 1-2 hr. Prepare a separate compound plate from which ligands of interest will be added to the biosensor plate during the assay. For these assays, 25.0 µl of solution containing compound was added to each well on the biosensor plate for a total volume of 50.0 µl. As such, compounds in solution were prepared in 2x the desired final concentration. 5. Perform the RWG Optical Biosensor Assay Take a baseline measurement with the Scanner system for wells A1-P12 (half of the SBS 384-well plate) using a maximum resolution of 3.75 µm/pixel for the central 1.5 mm of each well using the BIND Scan software . This baseline scan will take approximately 30 min. Add 25.0 µl of the compound solutions to each well for wells A1-P12. Take a baseline measurement of wells A13-P24. Add 25.0 µl of the compound solutions to each well for wells A13-P24. Take a post compound addition measurement for wells A1-P12, and repeat for wells A13-P24. 6. Analysis of Assay Data with BIND View Open the BIND assay data for the baseline measurement in Windows, and click the "Grid Editor" button to enable cell selection. The software will calculate metrics of interest defined by the user. Open the "Plug-ins", which include the "Cell Finder" and "Baseliner" function. Set parameters in "Cell Finder" so that cells are distinguishable from the background of the biosensor. Export the cell map file which contains the "Cell Finder" data for the baseline measurement. Repeat steps 6.1-6.2 for post compound addition data. Open the "Baseliner" plug-in and import the cell map from the baseline measurement. The software will calculate the shift in PWV between the background and post compound data. Select "Δ Cell Mean" for the output of the mean shift in PWV for cells. The data can then be exported to Microsoft Excel for further analysis.

Representative Results

Slack-B stably transfected HEK-293 cells and control untransfected HEK-293 cells were seeded at 1,000 cells/well on 384-well, ECM coated RWG biosensor plates. Images from the central 1.5 mm2 of the biosensor were recorded at a resolution of 3.75 µm/pixel (Figure 1). Density gradient maps of mass were generated pre and 30 min post compound addition with the BIND Scan software. The BIND View software was utilized to determine the shift in PWV upon GPCR agonist addition by sub…

Discussion

The Z prime (Z') factor is a common statistical method to quantify the quality of a high-throughput screening assay²⁰, and because the screening of the GPCR agonists in this assay occurred in a SBS compatible 384-well assay, provides an excellent measure of the robustness and validity of this assay²¹. A Z' value of 1 indicates a theoretically ideal assay with an infinite number of data points with nonexistent standard deviations. A Z' value of between 0.5-1 is considered an excellent ass…

Materials

DMEM, High Glucose	Life Technologies	11965-092
Leibovitz's L-15 Medium	Life Technologies	11415-064
Penicillin-Streptomycin (10,000 U/ml)	Life Technologies	15140-122
Geneticin G-418 Sulfate	American Bioanalytical	AB05057
HBSS	Life Technologies	14025-092
Fibronectin from human plasma	Sigma-Aldrich	F0895
Albumin from chicken egg white	Sigma-Aldrich	A5378
DPBS	Life Technologies	14190-144
Hausser Bright-Line Phase Hemocytometer	Fisher Scientific	02-671-6
Carbamoylcholine chloride	Sigma-Aldrich	C4382
SFLLR-NH2 trifluoroacetate salt	Sigma-Aldrich	S8701
Finnpipette (5-50 µl)	Thermo Scientific	4662090
BIND Scanner System	X-BODY Biosciences	N/A
384-well TiO2 coated plates	X-BODY Biosciences	TiO-96-CM