Materials and Reagents

Screw cap glass vials with PTFE screwcap (Spectrum Chemical, catalog number: 985-92215)
Cuvette spinbar (VWR, catalog number: 58949-030)
Quartz UV cuvette (Fireflysci, catalog number: 1FLUV10)
515 nm filter (Andover Corporation, catalog number: 515FG05-50S)
1 ml syringe (BD, catalog number: 309659)
9’’ Pasteur pipet (Fisher scientific, catalog number 13-678-6b)
Saint-Gobain Tygon tubing (Saint-Gobain, catalog number: ACF00017F)
Glass tube rack (Fisher Scientific, catalog number: K7492100100)
HiTrap^® desalting columns (Millipore-Sigma, catalog number: GE17-1408-01)
Gel loading pipet tips (Fisherbrand, catalog number: 02-707-139)
10 mm filter supports (Avanti Polar Lipids, catalog number: 610014)
0.2 µm membrane (Whatman, catalog number: 800281)
Aluminum foil (Fisherbrand, catalog number: 01-213-100)
1 ml sample loop (Thermo Scientific, catalog number: 03-052-382)
Chloroform (Fisher Chemical, catalog number: c298)
1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC) (Avanti Polar Lipids, catalog number: 850375)
1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl) iminodiacetic acid) succinyl] (nickel salt) (18:1 DGS-NTA(Ni) (Avanti Polar Lipids, catalog number: 790404)
1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt) (POPG) (Avanti Polar Lipids, catalog number: 840457)
1-palmitoyl-2-oleoyl-glycero-3-phosphocholine (POPC) (Avanti Polar Lipids, catalog number: 850457)
Ethanol (Fisher Chemical, catalog number: a4094)
HPLC grade water (Fisher Chemical, catalog number: W5-4)
Tris-base (Fisher Chemical, catalog number: BP152)
Sodium chloride (Fisher Chemical, catalog number: BP358)
Sodium hydroxide (Fisher Chemical, catalog number: S318)
Hydrochloric acid (Fluka, catalog number: 7647)
Dry ice
4-(2-Hydroxyethyl)piperazine-1-ethanesulfonic acid, N-(2-Hydroxyethyl)piperazine-N′-(2-ethanesulfonic acid) (HEPES) (Fisher Bioreagents, catalog number: BP310)
8-Aminonaphthalene-1,3,6-trisulfonic acid, disodium salt (Setareh Biotech, catalog number: 6951)
p-Xylene-bis-pyridinium bromide (DPX) (Setareh Biotech, catalog number: 6271)
Triton X-100 (Sigma-Aldrich, catalog number: X100)
Sodium acetate (Sigma-Aldrich, catalog number: S2889)
Methanol (Fisher, catalog number: A453-500)
Gel filtration buffer (see Recipes)
pH 4 buffer (see Recipes)

Equipment

Glass tubes (VWR, catalog number: 89000-502)
50 ml beaker (Pyrex, catalog number: 02-540G)
Lab mounting stand (Humboldt MFG Company, catalog number: H-21217)
Nitrogen gas tank
Gas tank regulator (VWR, catalog number: 55850-277)
Large top desiccator (Corning Life Sciences, catalog number: CLS3120250)
Hot plate/stirrer (Thermo Fisher Scientific, catalog number: SP131325)
Extruder set with heating block (Avanti Polar Lipids, catalog number: 610000)
pH meter (Mettler Toledo, catalog number: 30266626)
Vortex (VWR, catalog number: 58816-121)
Scale (Mettler Toledo, catalog number: ML54)
AKTA FPLC system (General Electric, catalog number: UPC-900 and P920)
Fluorometer (ISS, catalog number: K2)
Water bath (VWR, catalog number: 13271-086)

Procedure

Drying phospholipids
1. If working with lipid powders, create a lipid stock solution.
2. Measure 50-150 mg of lipids into a glass vial with a screw cap.
3. Add 5-15 ml of 3:2 chloroform:methanol as needed to maintain concentration at 10 mg/ml for ease of usage.
  Note: Cover the vial using PTFE lined caps; otherwise, the chloroform may dissolve plastics and contaminate the sample.
4. Measure the appropriate amount of lipids (10 mg will be enough for approximately 30 reactions) into a glass tube.
  Note: Liposomes can be made of single lipid forms [e.g., 1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (sodium salt) (POPG), and 1-palmitoyl-2-oleoyl-glycero-3-phosphocholine (POPC)] or their combinations. For example, the Ni²⁺-chelating lipid, 1,2-dioleoyl-sn-glycero-3-[(N-(5-amino-1-carboxypentyl) iminodiacetic acid) succinyl] (nickel salt) or (DGS-NTA(Ni)), can attach His-tagged proteins to the membranes (Sun et al., 2007 and 2008; Jacquez et al., 2014). The new liposome developed for measuring the MPA of EsxAB is composed of POPC to POPG at a 4:1 molar ratio.
5. Use a clamp stand to hold the vial in place.
6. Using a second clamp, position a Pasteur pipette approximately 2-5 mm away from the liquid in the tube.
7. Connect the tubing to the end of the Pasteur pipette and open the valve to allow gentle airflow.
8. Evaporate the chloroform from the vial until there is no liquid visible.
9. Remove the vial from the stand and place it inside a vacuum chamber at room temperature for at least 3 h or overnight.
10. Store the dry lipids at -20 °C. Lipids may be stored under these conditions for up to a month.
Preparing column and FPLC for desalting
1. A 5-ml desalting column is needed for removing the excess ANTS/DPX and for buffer exchange. If necessary, two desalting columns can be connected in tandem to improve desalting results.
2. Pass at least 5 column volumes (CV) or, in this case, 50 ml of water through the column to remove the ethanol from the column.
3. Pass at least 5 CV (50 ml) of gel filtration buffer through the column.
4. Prepare the machine for desalting by passing 50 ml of water through the machine at 5 ml/min.
5. Pass 50 ml of gel filtration buffer through the machine at 5 ml/min.
6. Connect the column to the machine and pass an additional 100 ml of gel filtration buffer.
7. Clean the injection valve by injecting 1 ml of gel filtration buffer.
8. Repeat Step B7 at least two more times.
Preparing the lipid-ANTS/DPX solution
1. Prepare a freezing solution in a beaker by adding dry ice to > 95% ethanol. The freezing solution is used to flash freeze the lipids containing ANTS/DPX. Alternatively, liquid nitrogen can be used to flash freeze. It is ideal to keep the freezing solution below -50 °C.
2. Fill another beaker with lukewarm water for thawing the lipids.
3. Re-suspend lipids in 5 mM HEPES (pH 7.4), 1 ml for every 10 mg of lipids.
4. Vortex until the solution is well suspended.
5. Measure the solution volume and add 50 mM of ANTS and DPX into the tube.
6. Mix by pipetting up and down and cover the tube with aluminum foil.
7. Place the tube into the freezing solution and allow it to freeze.
8. Move the tube into warm water to thaw the lipids.
9. Repeat Steps C7-C8 for five more freeze/thaw cycles.
  Note: Six freeze/thaw cycles are usually sufficient to solubilize the lipids. If problems occur during the extrusion, such as difficulties in passing the liquid through the membranes, perform more freeze/thaw cycles.
Producing liposomes via extrusion
1. Assemble the extruder according to the manufacturer’s specifications.
2. Draw up 1 ml of gel filtration buffer using one of the syringes and pass the buffer through the extruder until the liquid has been transferred to the other syringe.
  Note: You should feel a little bit of resistance. If there is no resistance, it is possible the membrane has moved during assembly or has torn.
3. Remove the buffer from the syringe.
4. Draw up to 1 ml of liposomes into one of the syringes.
5. Pass the liposomes through the membrane until the liquid has been transferred from one syringe to the other.
6. Repeat Step D5 for a total of 20 times.
7. Inspect the fluid after extrusion; it should have changed from an opaque to a transparent, yellow-tinged liquid (Figure 1).
  
  Figure 1. Comparison of the lipid solution before and after extrusion. A. The lipid solution before extrusion has an opaque color. B. The lipid solution becomes more transparent after extrusion.
8. Dispense the lipids into a clean glass tube.
Removal of excess fluorescent dyes via desalting chromatography
1. After pre-equilibration of the column and machine and cleaning the injection loop, inject the liposomes into the injection loop.
2. Run the desalting program at a 0.5 ml/min flow rate, using gel filtration buffer, and collect 0.5 ml per fraction.
3. Allow 50 ml of buffer to pass through the column.
4. The liposomes will be eluted out of the column after approximately 2 ml have passed through.
5. Collect fractions containing the liposomes, usually in six tubes for a total 3 ml of liposomes (Figure 2).
  
  Figure 2. Most lipids will elute after flowing approximately 2 ml of buffer through the column. A typical yield of 3 ml is expected using this procedure. The blue line represents mAu, and the brown line represents conductance.
6. Combine all liposome samples, cover with aluminum foil, and store at 4 °C.
7. Liposomes at this stage can be stored for approximately 1-3 weeks.
8. Liposomes prepared with this procedure are usually consistent in concentration. However, technical replicates with the same batch of lipids are needed for every biological replicate to obtain consistent results.
9. Clean the column by passing at least 5 CV + 30 ml (the volume of the machine) of water through the machine.
10. Pass at least five CV in addition to 30 ml of 20% ethanol through the machine for column storage.
Liposome leakage assay
1. The quality of the liposomes should be tested before analyzing the protein of interest by adding 2% (v/v) Triton X-100, which completely lyses the liposomes, quickly revealing a strong fluorescence signal.
2. Set fluorometer excitation to 350 nm and record emissions at 520 nm and continue to measure at 1-second intervals for 5-10 min.
3. Cross polarizers are applied at the excitation and emission paths to reduce background. If necessary, apply a 515 nm long-pass filter at the emission path to reduce background scatter.
4. If available, connect a water bath to the water inlet and outlet of the sample chamber to maintain a constant temperature. This is especially important with proteins that interact at the physiological temperature, as is the case with EsxAB.
5. To a UV cuvette, add 1.15 ml of gel filtration buffer, 150 µl of 1 M NaAc buffer (pH 4), and 100 µl of liposomes.
6. Place the sample cuvette inside the sample chamber and close the lid.
7. After approximately 30 s, use a gel loading pipette tip to inject 100 µl of 2% Triton X-100 into the cuvette through the hole on the cover lid. The ANTS fluorescence should increase at least 5-fold (Figure 3). This will serve as a positive control.
  1. The fluorescence intensity will drop for a second or two due to the dilution of the mix inside the cuvette, but it will begin to rise shortly after.
  2. A negative control consists of the sample prepared with liposomes and the gel filtration buffer.
8. Continue experimenting by testing cytolytic proteins; prepare the cuvette as in Step F5 (Figure 3).
  
  Figure 3. Raw plots of an ANTS/DPX assay. The background fluorescence intensity is approximately 100,000 units. The fluorescence intensity increased 5-fold after adding 2% Triton X-100. With EsxA, a protein known to have MPA, we observed a gradual increase in fluorescence. EsxB, a protein without MPA, did not increase fluorescence intensity. The negative control consisting of the only gel filtration buffer did not increase fluorescence intensity.
9. Place the UV cuvette in the sample chamber and close the lid.
10. After about 30 s, use a gel loading pipette tip to add 100 µl of protein into the cuvette.
  1. Protein concentrations can vary, but a total of 100 µg is usually used in our experiments.
  2. Depending on the nature of the experiment, the protein can be loaded into the cuvette instead of the pH 4 buffer. Then, after 30 s, adding the pH 4 buffer will cause EsxAB to lyse the membrane.

Data analysis

The fluorescence intensity is normalized at the time point the protein was added by subtracting the lowest intensity value from all other values, removing the background fluorescence.
The lowest intensity value is now deemed the measurement at T = 0, and all values from T = 0 until the end of the experiment are averaged for all replicates.
The dilution of the lipids by adding the sample results in a small drop in fluorescence. Measuring from the moment the protein is added allows determination of the increase in fluorescence as the liposomes are lysed.
The average intensity is graphed against the time to obtain a curve (Figure 4A).
The plateau followed by a one-phase association can also be used to obtain an association constant.
The average of the highest fluorescence intensity values for each sample are graphed in a bar graph (Figure 4B).

Figure 4. Plot of sample liposome experiment after normalization. A. The data were normalized to remove background fluorescence and to account for the drop in fluorescence caused by the dilution of the liposomes by the sample. B. The peak fluorescence was graphed with error bars representing the standard deviation. Statistical significance is represented here as well.
The values are tested for normality using the Shapiro-Wilk test.
If the data fails to differ from normal, it is tested for significance with a One-way ANOVA; otherwise, a Tukey-Kramer test is performed.

Recipes

Gel filtration buffer
20 mM Tris, pH 7.4
10 mM NaCl
pH 4 Buffer
1 M NaAC, pH 4.01

Acknowledgments

This study was supported by grants from NIGMS (SC1GM095475 to J. Sun), National Center for Research Resources (5G12RR008124), and National Institute on Minority Health and Health Disparities (G12MD007592). Javier Aguilera was supported by a National Institutes of Health Grant (R25GM069621 to R. Aguilera) via the RISE program for graduate students. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

This protocol was adapted from Nieva et al.,1989 (DOI: 10.1021/bi00444a032) and optimized for the EsxA/EsxB complex.

Competing interests

Authors have no competing interests to declare.

References

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