Bioluminescence Resonance Energy Transfer (BRET)-Based Assay for Measuring Interactions of CRAF with 14-3-3 Proteins in Live Cells

Summary

This protocol describes a BRET-based assay for measuring the interactions of the CRAF kinase with 14-3-3 proteins in live cells. The protocol outlines steps for preparing the cells, reading BRET emissions, and data analysis. An example result with identification of appropriate controls and troubleshooting for assay optimization is also presented.

Abstract

CRAF is a primary effector of RAS GTPases and plays a critical role in the tumorigenesis of several KRAS-driven cancers. In addition, CRAF is a hotspot for germline mutations, which are shown to cause the developmental RASopathy, Noonan syndrome. All RAF kinases contain multiple phosphorylation-dependent binding sites for 14-3-3 regulatory proteins. The differential binding of 14-3-3 to these sites plays essential roles in the formation of active RAF dimers at the plasma membrane under signaling conditions and in maintaining RAF autoinhibition under quiescent conditions. Understanding how these interactions are regulated and how they can be modulated is critical for identifying new therapeutic approaches that target RAF function. Here, I describe a bioluminescence resonance energy transfer (BRET)-based assay for measuring the interactions of CRAF with 14-3-3 proteins in live cells. Specifically, this assay measures the interactions of CRAF fused to a Nano luciferase donor and 14-3-3 fused to a Halo tag acceptor, where the interaction of RAF and 14-3-3 results in donor-to-acceptor energy transfer and the generation of the BRET signal. The protocol further shows that this signal can be disrupted by mutations shown to prevent 14-3-3 binding to each of its high-affinity RAF docking sites. This protocol describes the procedures for seeding, transfecting, and replating the cells, along with detailed instructions for reading BRET emissions, performing data analysis, and confirming protein expression levels. In addition, example assay results, along with optimization and troubleshooting steps, are provided.

Introduction

RAF kinases (ARAF, BRAF, and CRAF) are the direct effectors of RAS GTPases and the initiating members of the pro-proliferative/pro-survival RAF-MEK-ERK kinase cascade. Recent studies have shown that CRAF expression plays a key role in the tumorigenesis of several KRAS-driven cancers, including non-small cell lung cancer and pancreatic ductal adenocarcinoma^1,2,3,4,5. Moreover, germline CRAF mutations cause a particularly severe form of the RASopathy, Noonan syndrome^6,7. Understanding CRAF regulation is critical for developing successful therapeutic approaches that target its function in cells.

All RAF kinases can be divided into two functional domains, a C-terminal catalytic (CAT) domain and an N-terminal regulatory (REG) domain, that controls its activity (Figure 1A)⁸. The REG domain encompasses the RAS binding domain (RBD), the cysteine-rich domain (CRD), and a serine/threonine-rich region (S/T-rich). Notably, the S/T-rich region contains the N' site, which binds to 14-3-3 in a phosphorylation-dependent manner (S259 in CRAF; Figure 1A)⁸. The CAT domain encompasses the kinase domain, along with a second high-affinity 14-3-3 docking site, referred to as the C' site (S621 in CRAF; Figure 1A)⁸. The differential binding of dimeric 14-3-3 proteins to the N' and C' sites, along with the CRD, plays critical roles in both RAF activation and inhibition^{9,10,11,12,13}. Under normal signaling conditions, RAF activation is initiated by its recruitment to the plasma membrane by RAS, allowing it to form active dimers, of which the BRAF-CRAF heterodimer is the predominant active form^14,15. Biochemical assays with BRAF and CRAF, along with cryogenic electron microscopy (Cryo-EM) structures of dimeric BRAF, indicate that a 14-3-3 dimer stabilizes active RAF dimers by binding simultaneously to the C' site of both RAF protomers (Figure 1B)^9,13,16,17. Conversely, studies have shown that under quiescent conditions, RAF adopts a cytosolic, autoinhibited confirmation, where the REG domain binds to the CAT domain and inhibits its activity^12,18,19,20. This closed state is stabilized by a 14-3-3 dimer bound to the CRD and N' site in the REG domain and to the C' site in the CAT domain (Figure 1B)^10,13,21. In BRAF, this model is supported by recent Cryo-EM structures of autoinhibited BRAF monomers and by our previous biochemical studies^{10,12,13,21,22}. However, while 14-3-3 is shown to play an inhibitory role in CRAF regulation²³, a BRAF-like autoinhibited state may play a lesser role in CRAF regulation¹²; therefore further studies are required to clarify the mechanisms by which 14-3-3 proteins regulate CRAF activity. The 14-3-3-mediated regulation of RAF kinases requires a plethora of RAF phosphorylation and de-phosphorylation events, the binding to various regulatory proteins, and interactions with the plasma membrane⁸. Therefore, it is critical that 14-3-3-RAF interactions are measured under physiologically relevant conditions and in the presence of an intact lipid bilayer.

To address this issue, NanoBRET (from here on referred to as N-BRET; see Table of Materials for kit details) technology was utilized to develop a proximity-based assay for measuring the interactions of CRAF with 14-3-3 proteins in live cells (Figure 1C). This BRET-based system measures the interactions of two proteins of interest (POI), where one protein is tagged with a nanoluciferase (Nano) donor and the other with a Halo tag, for labeling with the Halo618 energy acceptor ligand^22,24. Interaction of the proteins of interest results in donor to acceptor energy transfer, which in turn generates the BRET signal (Figure 1C). The extremely bright Nano donor protein (emission (em) 460 nm) and the Halo618 ligand (em 618 nm) provide greater spectral separation and sensitivity over conventional BRET, making it an ideal platform for studying weaker interactions and detecting subtle changes in binding²⁴. Indeed, we previously developed a N-BRET-based assay for measuring the autoinhibitory interactions of the RAF REG and CAT domains, which was essential for the characterization of a panel of RASopathy mutations in the BRAF CRD and demonstrated the critical importance of this domain for maintaining autoinhibition and preventing constitutive BRAF activation¹².

The assay described here measures the interactions of CRAF, fused to an N-terminal Nano tag (Nano-CRAF), and the zeta isoform of 14-3-3 fused to C-terminal Halo tag (14-3-3ζ-Halo; Figure 1C). We show that the interactions of Nano-CRAF with 14-3-3ζ-Halo generates a robust BRET signal, which can in turn be disrupted by mutations which prevent 14-3-3 binding to the N' site (S259A) and/or the C' site (S621A). The following protocol provides detailed steps for performing, optimizing, and troubleshooting this assay.

Protocol

NOTE: This assay is performed in 293FT cells. A well characterized and readily transfectable epithelial line derived from human embryonic kidney cells. A single confluent 10 cm culture dish of these cells typically provides enough cells for seeding 20 wells of 6-well tissue culture plates. Steps 1-3 must be performed using sterile technique in a biological safety cabinet.

1. Cell seeding (Day 1)

NOTE: In this step, the cells are detached from the tissue culture dish(s), counted, and seeded in 6-well tissue culture plates for transfection in step 2 (Figure 2).

1. Aspirate the media from the cells in the 10 cm dish. Wash cells with 5 mL of phosphate-buffered saline (PBS) and aspirate.
2. Add 1 mL of trypsin-ethylenediaminetetraacetic acid (EDTA) and incubate for 3-5 min at 37 °C to detach cells from the dish.
3. Add 9 mL of complete Dulbecco's modified eagle medium (DMEM) to the cells to neutralize trypsin and pipette up and down repeatedly to generate a homogenous single cell suspension.
4. Immediately transfer 20 µL of cells to a 1.7 mL tube and mix with 20 µL of trypan blue stain. Count cells using either an automated cell counter (Table of Materials) or hemocytometer.
5. Dilute cells to 2 x 10⁵ cells/mL in complete DMEM media and add 2 mL to each well of a 6-well tissue culture plate (4 x 10⁵ cells/well). Incubate cells at 37 °C and 10% CO₂ overnight.
   NOTE: It is recommended to use 293FT cells that have been passaged less than 20x. We have previously found that using cells with greater passage numbers can result in reduced BRET ratios and increased well-to-well signal variability.

2. Cell transfection (Day 2)

NOTE: Here, the cells are transfected with the pCMV5-NanoLuc-CRAF and pCMV5-14-3-3ζ-Halo expression constructs, along with pCDNA3.1 empty vector (Figure 2).

1. Prior to transfection, dilute the N-BRET plasmids to 5 ng/µL and pCDNA3.1 to 100 ng/µL, and number a set of sterile 1.7 mL tubes.
2. Add 100 µL of transfection media (see Table of Materials for details) to each tube, along with 5 ng of pCMV5-NanoLuc-CRAF, 10 ng of pCMV5-14-3-3ζ and 200 ng of PCDNA3.1.
3. Add 2 µL of transfection reagent (see Table of Materials for details) and vortex gently to mix. Pulse spin the tubes briefly in a microcentrifuge to ensure that all liquid is collected at the bottom of the tubes and then incubate at around 25 °C for 15 min.
4. Add transfection complexes dropwise to cells and incubate at 37 °C/10% CO₂ for 16-20 h to allow the Halo- and Nano- tagged proteins to be expressed.
   NOTE: The addition of an empty vector (pCDNA3.1) carrier DNA is essential for achieving high transfection efficiency of the N-BRET expression constructs. Failure to add empty vector results in reduced expression levels of the 14-3-3ζ-Halo and Nano-CRAF proteins and in turn results in weak and inconsistent BRET ratios, as discussed previously²².

3. Cell replating (Day 3)

NOTE: In this step, the cells are transferred to a 384-well plate and either Halo 618 ligand (+ligand; Table of Materials) or DMSO (+vehicle) is added for reading the BRET emissions in step 4. The remaining cells are transferred to fresh 6-well culture plates for western blot analysis in Step 5 (Figure 2).

1. Collect the following materials and prepare the work area as described below.
   1. Using a 37 °C water bath, pre-warm trypsin-EDTA, along with both serum-free Assay Media and 10% FBS-supplemented Assay Media (see Table of Materials for details).
   2. Based on the number of samples to be measured, pre-label three sets of sterile 1.7 mL tubes (Set 1-3), and one set of sterile 15 mL conical bottom tubes. Equip a swing-bucket centrifuge with 15 mL tube inserts and pre-cool to 4 °C.
   3. Place the following items in the tissue culture hood: reagents reservoirs, 384-well tissue culture plates, 6-well tissue culture plates, a multichannel pipette and tips, cell counting slides/chambers and trypan blue stain (Table of Materials), along with 1.7 mL tube Sets 1-3.
2. Harvest and count the cells as described below.
   1. Aspirate the media from the 6-well plates and add 250 µL of trypsin-EDTA to the cells. Incubate the 6-well plates at 37 °C until the cells begin to detach (3-5 min).
   2. Add 1 mL of 10% FBS-supplemented assay media to each well to neutralize the trypsin and pipette up and down vigorously to generate a single-cell suspension.
   3. Transfer 1 mL of the cell suspension to the pre-labeled 15 mL tubes. Add another 1 mL of 10% FBS-supplemented assay media to each of the 15 mL tubes.
   4. Invert the tubes 5x to mix and immediately transfer 20 µL of cell suspension to tube Set 1.
   5. Centrifuge in the pre-cooled swing bucket centrifuge for 5 min at ~250 x g. During the centrifugation step, mix 20 µL of trypan blue cell stain with the cells in tube set 1 and then count the cells using either an automated cell counter or hemocytometer. A yield of 6-8 x 10⁵ cells/mL is typical.
   6. Remove the 15 mL tubes from the centrifuge and aspirate the media from the cell pellets. Resuspend the cell pellets to 2 x 10⁵ cells/mL in serum-free assay media and pipette vigorously to generate a single cell suspension.
      NOTE: The use of serum-free Assay Media is used to quiescence normal cell signaling pathways.
3. Replate cells in 384-well and 6-well plates as described below.
   1. Invert the 15 mL tubes several times to ensure a homogenous cell suspension and transfer 500 µL to 1.7 mL tubes set 2 and set 3.
   2. Add 0.5 µL of DMSO (+vehicle) to set 2 and 0.5 µL of Halo 618 ligand (+ligand) to tube set 3 and pipette to mix.
   3. Transfer the +vehicle and +ligand cell suspensions to separate wells of reagent reservoirs. Using the multichannel pipette (Table of Materials), transfer 40 µL of the +vehicle cell suspension from the reagent reservoirs to quadruplicate wells of the 384-well culture plate. Repeat this step for the +ligand cell suspensions.
   4. Transfer the remaining cells into fresh 6-well culture plates. Incubate the 384-well and 6-well plates overnight at 37 °C and 5% CO₂.

4. Reading BRET emissions (Day 4)

NOTE: In this step the nanoluciferase substrate (see Table of Materials for details) is added to the cells in the 384-well culture plate and the N-BRET acceptor (618 nm) and donor (460 nm) emissions are read (Figure 2). The corrected BRET ratios are then calculated.

1. Pre-warm serum-free assay media in a 37 °C water bath and thaw the nanoluciferase substrate at 25°C. Dilute the nanoluciferase substrate 1:100 in serum-free assay media and transfer to a reagent reservoir. Prepare enough of this mixture for adding 10 µL to each well of the 384-well plate, plus 10%-15% extra volume.
2. Using a multichannel pipette (Table of Materials), transfer 10 µL of the substrate mixture to each of the wells that contain cells in the 384-well culture plate. Gently rotate the plate for 1 min, either manually or using an orbital shaker.
3. Insert the 384-well plate into the multimode plate reader and record the 460 nm and 618 nm emissions for all wells that contain cells.
   NOTE: For the multimode plate reader used for this step (see Table of Materials for details), a read height of 6.5 mm, with a 0.1 s read time measurement was used, however further optimization may be required if using other plate readers.
4. Calculate the raw BRET ratios for +vehicle and +ligand in milliBRET units (mBU) individually, using the following equation:
   
5. Calculate the corrected BRET ratio by subtracting the +vehicle BRET ratio from that of the +Ligand (Supplementary Table 1).
   NOTE: When comparing the results of multiple experiments, the corrected BRET ratios can be pooled and normalized to the average of the Wildtype (WT) N-BRET pair, consisting of Nano-CRAF^WT and 14-3-3ζ^WT-Halo (Supplementary Table 1).

5. Confirmation of protein expression levels (Days 4 and 5)

NOTE: In this step the cells in the 6-well plates are lysed and the protein expression levels of the Nano-CRAF and 14-3-3ζ-Halo proteins are determined by western blot analysis using antibodies specific to the Halo and Nano tags. (Figure 2).

1. Add protease and phosphatase inhibitors to NP40 lysis buffer (Table of Materials), allowing 200 µL of lysis buffer per sample.
2. Aspirate media from 6-well plates that contain cells. Wash the cells once with 1 mL of cold PBS and aspirate.
3. Add 125 µL of NP40 lysis buffer to each well and incubate 6-well plates at 4 °C on a rocking platform for 15 min to lyse the cells.
4. Transfer lysates to 1.7 mL tubes on ice and centrifuge at 20,000 x g for 10 min at 4 °C. Place the cleared lysates back on ice and determine protein concentration using commercially available assays, such Bradford or Bicinchoninic acid (BCA) assays.
5. Normalize protein concentration across all samples by transferring an appropriate volume of lysate and NP40 lysis buffer to fresh 1.7 mL tubes to a total volume of 100 µL.
6. Boil 5x protein sample buffer (Table of Materials) for 1 min and add 25 µL to each sample. Boil samples for 5-6 min and then pulse centrifuge the tubes briefly to ensure all of the sample collects in the base of the tube.
7. Load 25 µL of sample into each well of duplicate protein gels (Gel 1 and Gel 2) and then transfer proteins to nitrocellulose or PVDF membranes using standard western blotting procedures, as previously described²².
8. Block membranes in 3% BSA-PBS at 25 °C for 30 min and then incubate membranes overnight with Halo antibody (1:1,000 dilution; Gel 1) and either nanoluciferase or CRAF antibody (1:500 dilution; Gel 2) in tris-buffered saline, supplemented with 0.2% Tween-20 (TBST; Table of Materials).
9. Wash membranes 1x for 5 min in 10 mL of TBST and then incubate at room temperature for 1 h with anti-mouse HRP secondary antibody, diluted 1:10,000 in TBST.
10. Wash membranes 3x on a rocking platform in 10 mL of TBST at 25 °C for 5 min each. Remove TBST and visualize protein bands using ECL reagents and either an X-ray film processor or other appropriate imaging system.

Results

When performed as described in this protocol (Figure 2), the interaction of Nano-CRAF^WT and 14-3-3ζ-Halo should produce corrected BRET ratios of 50-60 mBU (Figure 3A; Supplementary Table 1). CRAF contains two phosphorylation-dependent 14-3-3 docking sites, the N' site and the C' site (Figure 1)⁸. Therefore, appropriate controls for reducing CRAF:14-3-3ζ binding include S259A and S621A, which prevent phosphorylation, and in turn 14-3-3 binding, to the N' and C' sites, respectively²⁵. As shown in Figure 3A, Nano-CRAF^S259A reduces the BRET signal by ~45% and Nano-CRAF^S621A by ~25%, while the S259A/S621A (SS/AA) double mutant almost entirely ablates the CRAF:14-3-3 BRET signal. In addition, the results of multiple independent experiments can be compared by first normalizing the results of each experiment to the average corrected BRET ratio (Supplementary Table 1), and then pooling together the data points from all three experiments (Figure 3B). The relative expression levels of the tagged proteins should also be confirmed by western blot analysis (Figure 3). Note that the expression levels of mutant proteins may vary from that of WT requiring that the transfected amounts of mutant DNA vectors be adjusted accordingly (Supplementary Table 1).

It should also be noted that optimization of this protocol may be required, especially when using an alternative plate reader, cells lines, or transfection reagents. Figure 4A shows the results of an example optimization experiment, where increasing the transfected amount of the pCMV5-14-3-3ζ-Halo acceptor plasmid, while keeping the amount of pCMV5-NanoLuc-CRAF donor constant, dose dependently increases the BRET signal, which is then reduced by the presence of the 14-3-3-binding deficient CRAF^SS/AA mutant. However, if the acceptor to donor ratio is too high, the difference in signal between 14-3-3ζ-Halo binding to Nano-CRAF^WT vs the Nano-CRAF^SS/AA negative control will be reduced, likely reflected binding saturation of Nano-CRAF^WT. In addition, once a BRET ratio that generates reproducible values with low standard error is achieved, further increase in the acceptor to donor ratio is unnecessary. Indeed, one of the major advantages of these assays is the ability to measure the interactions of proteins at physiological expression levels. When developing new N-BRET assays, another important consideration is the tag placement. Figure 4B shows the effect of switching the Halo tag from the C-terminus to the N-terminus of 14-3-3ζ on the corrected BRET ratios generated by 14-3-3ζ binding to Nano-CRAF^WT and Nano-CRAF^SS/AA. To this end, DNA expression constructs for each of the possible tag locations should be generated (Figure 4C), and their effects on the BRET ratios of both the WT pair and that of a known negative control for binding should be evaluated.

Figure 1: RAF regulation by 14-3-3 proteins. (A) RAF kinase domain structure schematic with conserved 14-3-3 docking sites indicated. (B) Models of RAF regulation by 14-3-3 proteins. (C) N-BRET assay measuring the interactions of 14-3-3ζ fused to a C-terminal Halo tag acceptor and CRAF fused to an N-terminal Nano donor. Donor to acceptor energy transfer generates the BRET signal. Please click here to view a larger version of this figure.

Figure 2: Key steps for performing the CRAF:14-3-3 live cell BRET-based assay. Shown are the five major steps outlined in this protocol, including: seeding, transfecting, and replating the cells, along with methods for reading the BRET signal and confirming the expression levels of the Halo- and Nano- tagged proteins. Please click here to view a larger version of this figure.

Figure 3: CRAF:14-3-3 BRET-based assay. N-BRET assay comparing the interactions of 14-3-3ζ-Halo with either Nano-CRAF -WT, or the -S259A, -S621A, and -S259A/S621A (SS/AA) mutant forms, shown previously to impair CRAF:14-3-3 binding²⁵. Expression levels of the 14-3-3ζ-Halo (MW: 64 kDa.) and the Nano-CRAF variants (MW: 93 kDa.) were examined by western blot analysis. (A) Corrected BRET readings from four replicate wells from a single experiment ± standard deviation (SD). (B) Corrected BRET readings from three independent experiments were pooled and normalized to Nano-CRAF^WT (set to 100) ± SD. Statistical significance was calculated by Student’s t test (two-tail, assuming equal variance). ****p<0.0001. Please click here to view a larger version of this figure.

Figure 4: Assay optimization steps. The effects of co-transfecting increasing amounts of (A) 14-3-3ζ-Halo or (B) Halo-14-3-3ζ with a constant amount of Nano-CRAF -WT or -SS/AA (S259A/S621A) on the BRET signal ± SD. (C) Schematic of all possible N-BRET pairs generated by placing the Halo or Nano tag on either the N-terminus or C-terminus of each protein of interest (A and B). n = 4. Please click here to view a larger version of this figure.

Supplementary Table 1: Example data from the CRAF:14-3-3 BRET-based assay. The indicated expression constructs were transfected into the cells on Day 2 (top section). The raw, corrected, and normalized BRET readings were measured and calculated on Day 4 (bottom section). Please click here to download this File.

Discussion

Previous studies have shown that 14-3-3 proteins play critical roles in both the activation and inhibition of RAF kinases. Understanding how these binding events are regulated and the effects of modulating these interactions on RAF signaling and RAF-driven oncogenesis may uncover new therapeutic vulnerabilities that target CRAF function. However, the Raf activation cycle is supported by a plethora of associated proteins, post translational modifications, and changes in subcellular localization⁸, and therefore to fully recapitulate these conditions, the interactions of RAF with its regulators must be measured under live cell conditions. This protocol describes a novel proximity-based assay which utilizes the superior signal to noise ratio and spectral resolution of the nanoluciferase-Halo N-BRET pair for measuring the interactions of 14-3-3ζ and CRAF in live cells.

While this assay provides a much-needed platform for studying the complex interactions of 14-3-3 and CRAF under physiologically relevant conditions, it has a number of limitations which should be considered. Firstly, given that 14-3-3 has been shown to play roles in both RAF autoinhibition and dimerization⁸, additional controls and experimental approaches may be incorporated to distinguish between these states. For example, this assay can be performed in conjunction with the previously developed N-BRET autoinhibition assay which provides a direct readout of changes in RAF autoinhibition^12,22. Moreover, controls such as the CRAF R401H mutation, shown to disrupt the dimerization of CRAF with other RAF protomers^15,26, may also prove useful in dissecting these functions. Finally, the placement of the Halo and Nano tags is optimized for measuring the CRAF:14-3-3 interaction but cannot guarantee that the interactions of CRAF or 14-3-3 with other proteins are not affected as a result, nor can this assay determine the affinity of CRAF:14-3-3 binding, the effects of these interactions on CRAF activity, or the location in the cell at which these interactions occur. Therefore, it may also be necessary to incorporate other complimentary approaches, such as in vitro binding assays, CRAF kinase assays and subcellular localization studies^12,27,28,29.

When performing this assay, or indeed any N-BRET-based assay, there are a number of factors to be considered. As shown in this manuscript, and in previous work²², the correct transfection ratio of the pCMV5-Halo (acceptor) and the pCMV5-Nanoluciferase (donor) constructs, along with an appropriate negative control, such as a mutant known to disrupt binding of the POIs, is critical for optimizing and testing these assays. Increasing the expression of the Halo tagged POI, while keeping the levels of Nano tagged POI constant, results in increased BRET ratios. However, once binding is saturated the signal will level off and in turn the delta between the WT and binding-impaired POIs will be reduced, necessitating acceptor-donor optimization. Another critical factor in assay optimization is the use of an empty vector carrier DNA, such as pCDNA3.1. The inclusion of 200 ng of pCDNA3.1. in the transfection mix greatly increases the expression levels of the Halo- and Nano- tagged POIs and reduces the variability between replicate wells and experiments²². However, given that transfection efficiency can vary between reagents and cell lines, the amount of carrier DNA may also need to be titrated to achieve optimal expression of the N-BRET pair, as described previously²². Another factor that greatly affects the BRET ratios is tag placement. Indeed, which POI is fused to the Halo tag vs. the Nano tag and whether this tag is placed on the N- or C-terminus of the protein can affect both the amplitude of the BRET ratio and the ability of negative controls to reduce this signal. Therefore, it is also important to test out each of the possible N-BRET pairs when developing new assays.

The improved sensitivity and spectral resolution achieved by N-BRET over conventional BRET allows for weaker interactions and subtle changes in binding to be measured in live cells. However, the utility of these assays for studying cell signaling events has not been fully realized. Notably, this assay could likely be adapted for studying the interaction of 14-3-3 with other kinases, such as fellow RAF kinases ARAF and BRAF, and when combined with previously published N-BRET assays for studying RAS:RAF binding and RAF autoinhibition^22,30, will form the basis of a tool-kit for measuring RAF regulation under live cell conditions. In addition, N-BRET has shown promise as a live cell drug screening platform³⁰, and therefore this assay may also be of use for identifying compounds that either stabilize the inhibitory with interactions of 14-3-3 and RAF or disrupt those involved in RAF activation. Given the high stability of the nanoluciferase signal and the ability of modern plate readers to simultaneously detect acceptor and donor emissions, it would also follow that these assays can be adapted for measuring the interactions of signaling proteins in real-time, which will be critical for understanding the dynamics of these interactions in response to upstream stimulation or drug treatments.

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Antibodies
HaloTag® mouse monoclonal antibody	Promega	G9211	Antibody for detecting HaloTag tagged  proteins by immunoblot
NanoLuc® mouse monoclonal antibody	R&D Systems	MAB10026	Antibody for detecting Nano-tagged proteins by immunoblot
CRAF mouse monoclonal antibody (E10)	Santa Crus Biotechnology	sc-7267	Antibody directly detecting CRAF proteins by immunoblot
ECL anti-mouse HRP secondary antibody	Amersham	NA931-1ML	Secondary HRP conjugated mouse antibody (from sheep)
Reagents
X-tremeGENE™ 9	Roche/Sigma	6365809001
NanoBRET™ kit	Promega	N1661	NanoBRET kit containing Halo 618 ligand and NanoGlo (nanoluciferase) substrate
DPBS, without Ca++ and Mg++	Quality Biologicals	114-057-101
Trypsin-EDTA (0.05%), phenol red	Life Technologies	25300120
DMEM cell culture media	Life Technologies	11995073	High glucose, L-glutamine, phenol red, sodium  pyruvate; without HEPES, suppliment media with 10% FBS, 2 mM L-glutamine and 100U penicillin-streptomycin
L-Glutamine (200 mM)	Life Technologies	25030164
Penicillin-Streptomycin (10,000 U/mL)	Life Technologies	15140163
Opti-MEM™ I reduced serum media	Gibco	31985062	For cell transfection
Opti-MEM reduced serum media, no phenol red	Gibco	11058021	For replating cells on Day 3. Supplement with 2 mM L-glutamine and 100U penicillin-streptomycin, along with 10% FBS (where indicated).
Invitrogen Trypan Blue Stain	Thermo Scientific	T10282
NP40 lysis buffer	N/A	N/A	20 mM Tris (pH 8.0), 137mM NaCl, 10% glycerol,  NP40 alternative (Milipore, Cat# 492016). Store at 4 degrees C.. Add the following protease and phosphatase immediately prior to use: 20 µM leupeptin, 0.5 mM sodium orthovanidate, 0.15 U/mL, 1mM PMSF.
5x gel sample buffer	N/A	N/A	240 mM Tris (pH 8.0), 9.5% SDS, 30% glycerol, 500mM DTT, 3mM bromophenol blue. Store at -20 degrees C.
Cell lines
293FT cells (human)	Thermo Scientific	R70007
DNA vectors
pCMV5-Nano-CRAF WT and mutant	N/A	N/A
pCMV5-14-3-3ζ-Halo	N/A	N/A
Equipment
EnVision 2104 Multimode Plate Reader	PerkinElmer 2104	2104-0010	600LP NanoBRET & M460/50 nm NanoBRET emmisions filters,  Luminescence 404 mirror, 6.5 mm measurement height and 0.1 s measurement time
Invitrogen Countess™ II Automated Cell Counter	Thermo Scientific	AMQAX1000
ThermoFisher E1-ClipTip™  Multichannel  Pipettor	Thermo Scientific	4672070
Software
GraphPad Prism (version 10.0.3)	GraphPad	www.graphpad.com
Other
ThermoFisher ClipTip Multichannel pipette tips	Thermo Scientific	94410153
Reagent Reservoir, 25 mL Divided, Sterile	Thomas Scientific	1228K16
Perkin Elmer 384-well CulturPlate™	PerkinElmer	6007680	White, polystyrene, tissue culture treated
Countess Cell Counting Chamber Slides	Thermo Scientific	C10228