Use of Two Dimensional Semi-denaturing Detergent Agarose Gel Electrophoresis to Confirm Size Heterogeneity of Amyloid or Amyloid-like Fibers

Podsumowanie

Here we use two-dimensional semi-denaturing agarose gel electrophoresis to confirm the presence of amyloid-like fibers of heterogeneous size and exclude the possibility that the size heterogeneity is due to dissociation of the amyloid fibers during the gel running process.

Streszczenie

Amyloid or amyloid-like fibers have been associated with many human diseases, and are now being discovered to be important for many signaling pathways. The ability to readily detect the formation of these fibers under various experimental conditions is essential for understanding their potential function. Many methods have been used to detect the fibers, but not without some drawbacks. For example, electron microscopy (EM), or staining with Congo Red or Thioflavin T often requires purification of the fibers. On the other hand, semi-denaturing detergent agarose gel electrophoresis (SDD-AGE) allows detection of the SDS-resistant amyloid-like fibers in the cell extracts without purification. In addition, it allows the comparison of the size difference of the fibers. More importantly, it can be used to identify specific proteins within the fibers by Western blotting. It is less time consuming and more easily accessible to a wider number of labs. SDD-AGE results often show variable degree of heterogeneity. It raises the question whether part of the heterogeneity results from the dissociation of the protein complex during the electrophoresis in the presence of SDS. For this reason, we have employed a second dimension of SDD-AGE to determine if the size heterogeneity seen in SDD-AGE is truly a result of fiber heterogeneity in vivo and not a result of either degradation or dissociation of some of the proteins during electrophoresis. This method allows fast, qualitative confirmation that the amyloid or amyloid-like fibers are not partially dissociating during the SDD-AGE process.

Wprowadzenie

The formation of amyloid fibers due to protein misfolding has long been known to play a role in pathologic conditions such as Alzheimer's disease, Parkinson's disease, and Huntington's disease¹. More recently, the formation of amyloid or amyloid-like fibers has been shown to be a part of signaling pathways in humans, including during anti-viral innate immune response² and necroptosis^3,4, and in lower organisms such as yeast^5,6. Therefore, the ability to detect these fibers in the lab is important. Currently, there are three main ways to detect amyloid and amyloid-like fibers: the use of dyes, EM, and SDD-AGE.

The use of dyes, such as Congo Red or Thioflavin T, offers the advantage of being rapid and easily detectable using either microscopy or spectroscopy⁷. However, detection by microscopy, in the case of Congo Red, provides no specificity about which proteins comprise the fibers, or the size of the fibers. Similarly, the use of spectroscopy to detect Congo Red or Thioflavin T binding to protein complexes provides only a positive or negative result.

EM provides conclusive evidence of the presence of fibers and also quantitative information about the fiber length and diameter⁸. However, this method requires very stringent purification. Additionally, EM is a specialized technique which uses expensive equipment.

SDD-AGE has been used to detect SDS-resistant mega Dalton protein complexes including amyloid or amyloid-like fibers. It offers many advantages. First, it does not require the purification of the fibers and is easy to peform⁹. Second, it provides qualitative information about the size of the fibers, including relative size and amount of fiber heterogenicity. Lastly, because Western blotting can be performed after electrophoresis, it is easy to detect the presence of any protein for which there is an antibody, although it should be noted that because SDD-AGE is semi-denaturing, some epitopes may remain concealed which complicates detection by antibody.

Recently, receptor interacting protein kinase 1 (RIPK1) and 3 (RIPK3) have been reported to form amyloid fibers to serve as signaling platforms during necroptosis, a programmed form of necrosis³. While studying these fibers, our lab showed that another necroptosis-associated protein, mixed lineage kinase domain-like (MLKL), also formed amyloid-like fibers⁴. However, upon examination with SDD-AGE, the size of the MLKL fibers appeared distinct from the RIPK1 and RIPK3 fibers, which appeared identical to each other (Figure 1). This was unexpected because it is well-known that MLKL binds to RIPK1/RIPK3 to form the necroptosis signaling complex called the necrosome¹⁰.

There are at least two explanations. First, two totally distinct amyloid-like fibers may form during necroptosis, one containing RIPK1/RIPK3 and the other containing MLKL. Second, only one type of amyloid-like fibers containing RIPK1/RIPK3/MLKL may be formed during necroptosis, but the association of MLKL with the other proteins is weak enough that it dissociates during SDD-AGE.

To address this, we propose performing a two-dimensional (2D) SDD-AGE. SDD-AGE-stable amyloid or amyloid-like fibers will have the same migration pattern during the first and second dimension electrophoresis. This will be detectable after transferring the proteins to a membrane and carrying out a Western blot. Stable fibers will exhibit a sharp diagonal pattern. Any deviation from this would suggest that the fibers undergo changes due to the SDS-electrophoresis.

Protokół

1. Prepare Samples

1. Culture 2 x 10⁶ amyloid producing HT-29 colon cancer cells in a 10-cm tissue culture dish in 10 mL of Dulbecco's Modified Eagle Medium (DMEM) containing 10% fetal bovine serum and penicillin-streptomycin. Culture cells overnight in a 37 °C incubator with 5% CO₂.
   1. After the cells grow to 80% confluency, wash the cells with 10 mL of phosphate-buffered saline (PBS). Add 3 mL of Trypsin solution and incubate at 37 °C for 3 min.
   2. After the cells are totally dissociated from the dish, add 10 mL of culture medium and transfer the cells with a 10-mL pipette to a 15-mL conical tube. Centrifuge the cells at 1,000 x g for 3 min at room temperature. Aspirate the medium, resuspend the cells in 5 mL of culture medium, and count the cells using a cell counter. Plate 2 x 10⁶ cells in each of two 10-cm dishes.
   3. Allow the cells to adhere and recover overnight in a 37 °C incubator with 5% CO₂. Apply treatment to one dish to induce the formation of amyloids with 20 ng/mL Tumor Necrosis Factor-Alpha (TNF-α), 100 nM Smac-mimetic, and 20 µM pan-caspase inhibitor Z-VAD-FMK¹¹. The combination is abbreviated as TSZ. Treat the other dish with vehicle as a control.
2. After the appropriate length of time, usually 6 h, harvest the cell lysate.
   1. Scrape the cells off the plate with a plastic scraper and use a 10-mL pipette to transfer into a 15-mL conical tube. Centrifuge the cells at 1,000 x g for 3 min at 4 °C.
   2. Wash the cells 2 times by resuspending in 10 mL of ice cold PBS and centrifuging at 1,000 x g for 3 min at 4 °C. Aspirate the PBS solution.
      Note: The process can be paused here by freezing the cell pellet in liquid nitrogen and storing at ˗80 °C for up to 1 month.
   3. Transfer the cell pellet to a 1.5-mL microcentrifuge tube and incubate in 0.3 mL of lysis buffer for 30 min on ice. Centrifuge at 20,000 x g for 15 min at 4 °C. The supernatant is the whole cell lysate.
      Note: The process can be paused here by storing the sample at -20 °C for up to several months.
   4. Measure the protein concentration by a Bradford assay according to manufacturer's protocol. Add 4x SDD-AGE loading buffer to prepare 20 µL of 3 µg/µL sample and incubate at room temperature for 10 min.

2. Prepare and Run Gels

1. Add 2 g of agarose to 200 mL of 1x Tris-acetate buffer (TAE) in a glass beaker and heat in a microwave to melt the agarose. Add 1 mL of 20% SDS for a final concentration of 0.1% SDS. Carefully swirl to mix. Take care not to generate bubbles after the SDS addition.
2. Pour the agarose solution into a 15 cm x 14 cm gel slab. Use a 1-mL pipette to eliminate any bubbles. Place one 20-well comb at the top.
3. First dimension: Pipette 60 µg of whole cell lysate in the far-right lane. Run the gel at 60 V for about 4 h (until the dye front is about ¾ through the gel) using the TAE containing 0.1% SDS as the running buffer.
4. Second dimension: Carefully rotate the gel 90° counter-clockwise (Figure 2A). Run the gel at 60 V for about 4 h.
   Note: The general running condition is 4 V/cm gel length. It is important that the running conditions are exactly the same for the first and second dimensions.

3. Transfer

1. Use the capillary transfer method to transfer the proteins to a polyvinylidene difluoride (PVDF) membrane (Figure 2B).
   1. Add 500 mL of transfer buffer to an approximately 20 cm x 20 cm container. Make a 5-cm high stack of paper towels next to the container. The surface area of the top of the stack must be greater than the gel dimensions.
   2. Soak a 14 cm x 15 cm filter paper in transfer buffer and place on top of the paper towel stack. Take care to place on the paper with no wrinkles or bubbles. Repeat with another piece of filter paper.
   3. Activate a 14 cm x 15 cm PVDF membrane in methanol for 30 s then layer it on the filter paper taking care to use a roller to remove all bubbles. Rinse the gel off with transfer buffer and layer it on top of the membrane, again rolling out any bubbles.
   4. Cover the edge of the paper towels closest to the container of transfer buffer with plastic wrap. It is important that the paper bridge constructed in the next step does not come into direct contact with the paper towel stack.
   5. Soak a piece of 15 cm x 35 cm filter paper in transfer buffer and place it so one end covers the top of the gel and the other end is in the container of transfer buffer. Repeat with another bridge.
   6. Cover the container with plastic wrap and leave overnight at room temperature.

4. Western Blotting Detection

1. Rinse the membrane with 50 mL of PBS containing 0.05% Tween-20 (PBST) in a 20 cm × 20 cm container. Add 20 mL of 5% milk in PBST. Rock at room temperature for 30 min to block.
2. Pipette 10 µL of rabbit anti-MLKL antibody into 20 mL of 5% milk in PBST and add to the container. Incubate on rocker overnight at 4 °C.
3. Wash the membrane in 20 mL of PBST for 5 min. Repeat 5 times.
4. Pipette 4 µL of anti-rabbit-HRP to 20 mL of 5% milk in PBST and add to the container. Incubate on rocker at room temperature for 2 h.
5. Wash the membrane in 20 mL of PBST for 5 min. Repeat 5 times.
6. Add enhanced chemiluminescence substrate (ECL) and expose to X-ray films according to the manufacturer's protocol.

Wyniki

After necroptosis induction, RIPK1 and RIPK3 showed almost identical amyloid-like patterns (lanes 2 and 4, Figure 1). However, MLKL fibers were more heterogeneous and seemed to be smaller than RIPK1/RIPK3 fibers (lane 6, Figure 1). That prompted us to develop the 2D SDD-AGE method to address the possibility whether MLKL forms RIPK1/RIPK3-independent fibers or MLKL simply dissociates from the large RIPK1/RIPK3/MLKL fibers during S...

Dyskusje

The most critical aspect of the 2D SDD-AGE is that the electrophoresis conditions are the same for the first and second dimension. The ability to detect a sharp diagonal line at 45° (indicating that no dissociation or degradation has occurred) depends on the fibers migrating in an identical manner during both electrophoreses. Using different conditions, for example changing the voltage or the length of run time, will obscure these results. Also, as is the case for traditional 1D SDD-AGE, boiling the sample should be...

Materiały

Name	Company	Catalog Number	Comments
gel electrophoresis unit	Fisher	HE99XPRO	appratus for gel running.
agrose	VWR	97062-250	For agarose gel.
paper tower	Fisher	19-120-2484	for transfering
filter paper	VWR	21427-386	for transfering
PVDF membrane	Bio-Rad	162-0177	for transfering
blocking milk powder	Bio-Rad	1706404XTU	for blocking in Western blot
MLKL antibody	Genetex	GTX107538	rabbit anti-MLKL antibody
RIPK1 antibody	BD Biosciences	610459	mouse anti-RIPK1 antibody
RIPK3 antibody	gift from Dr. Xiaodong Wang		rabbit anti-RIPK3. See refenence 11.
anti-Rabbit-HRP	Sigma	A6154	secondary antibody
ECL	Fisher	WBKLS0500	Western chemiluminescent HRP substrate
X-ray film	Fisher	F-BX810	for Western blot result
DMEM	Sigma	D6429	for cell culture
fetal bovine serum	Sigma	F4135	for cell culture
penicilin-streptomycin	Sigma	P4333	for cell culture
Trypsin solution	Sigma	T4049	for cell culture
PBS for tissue culture	Sigma	D8662	for cell culture
recombinant TNF	made in our lab		for inducing necroptosis. See reference 11.
smac-mimetic	gift from Dr. Xiaodong Wang		for inducing necroptosis. See reference 11.
ZVAD-FMK	ApexBio	A1902	for inducing necroptosis. See reference 11.
Cell Counter	Bio-Rad	1450102	Model TC20; for counting cells
Pierce™ BCA Protein Assay Kit	Thermo Scientific	23225	for measuring protein concentration in cell lysates
Cell lifter	Fisher	07-200-364	to remove cells from dish
Lysis Buffer (1 L)			20 mL 1 M Tris pH 7.4 10 mL glycerol 30 mL 5 M NaCl 840 mL ddH2O 10 mL Triton-X100 (protease and phosphates inhibitors as desired)
10X TAE (1 L)			48.4 g Tris base 11.42 mL glacial acetic acid 20 mL 0.5M EDTA pH 8 ddH20 to 1 L
4X SDD-AGE loading buffer (50 mL)			5 mL 10X TAE 10 mL glycerol 4 mL 20% SDS 0.5 mL 10% bromophenol blue 31 mL ddH2O
TBS Transfer Buffer (1 L)			20 mL 1 M Tris pH 7.4 30 mL 5 M NaCl 950 mL ddH2O
PBST Wash Buffer (1 L)			100 mL 10xPBS 800 mL ddH2O 1 mL Tween20
10X PBS (10 L)			800 g NaCl 20 g KCl 144 g Na2HPO4·2H2O 24 g KH2PO4 add ddH2O to 10 L