Detection of protein ubiquitination in cultured cells

1. Transfect cultured cells with plasmids expressing the protein of interest and (epitope-tagged version of) ubiquitin.
2. Make complete cell lysis buffer (2% SDS, 150 mM NaCl, 10 mM Tris-HCl, pH 8.0) with 2mM sodium orthovanadate, 50 mM sodium fluoride, and protease inhibitors.
3. Lyse cells with 100 µl cell lysis buffer per plate (6 cm dish). If a larger dish is used, adjust volume accordingly.  Swirl the dish carefully to let the lysis buffer cover the entire area of grown cells.
4. Collect the cells with a cell scraper and transfer the cell lysates into a 1.5 ml eppendorf tube. Place the tube onto a hot plate immediately to boil for 10 min.
5. Shear the cells with a sonication device.
6. Add 900ul of dilution buffer (10 mM Tris-HCl, pH 8.0, 150 mM NaCl, 2 mM EDTA, 1% Triton). Incubate samples at 4°C for 30-60 min with rotation.
7. Spin the diluted samples at 20,000 x g for 30 min. Transfer the resulting supernatant to a new eppendorf tube. Be careful not to disturb the pellet.
8. Measure the protein concentration.
9. Prepare Protein A- or G-agarose bead-conjugated antibody against the target protein in a compatible buffer (50% slurry). Cut the narrow end of a P-200 pipette tip and transfer 14-20 μl of resin to 500-1,500 μg of prepared cell lysates for immunoprecipitation. For cells with high transfection efficiency, 500 μg will be enough. For cells with low transfection efficiency, more protein may be needed.
10. Incubate the cell lysate-bead mixture at 4°C overnight with rotation.
11. Spin down the beads at 5000 x g for 5 min. Aspirate the supernatant. Wash the resin with the washing buffer (10 mM Tris-HCl, pH 8.0, 1 M NaCl, 1 mM EDTA, 1% NP-40) twice.
12. Spin the beads for a final time at 20,000 x g for 30 sec. Aspirate the residual washing buffer and boil the resin with 2X SDS loading buffer.
13. Load samples onto a SDS-PAGE gel for immunoblotting analysis.
14. Detect ubiquitin and the target protein with respective antibodies. For immunoblotting, we generally detect ubiquitin first. The membrane will then be used to detect the protein precipitated.

Detection of ubiquitination on target protein through In vitro ubiquitination assay

1. Make 5X ubiquitination buffer (100 mM Tris-HCl, pH 7.5, 25 mM MgCl2, 2.5 mM DTT, 10 mM ATP). Store them in small aliquots at -20 °C for up to 6 month. Some protocols also add creatine phosphate and creatine kinase into the buffer for ATP regeneration ^1,2.
2. For each reaction, prepare a mixture containing the following:
   

   8 μl	5X ubiquitination buffer
   250 ng	ubiquitination E1
   500 ng	ubiquitination E2
   0.5 μg	ubiquitin
   0.5 μg	protein of interest
   	water to 40 μl total volume

   As controls, prepare similar reactions in the absence of either E1, E2, or ubiquitin.
3. Incubate the mixture at 37°C for 1 hour or longer.
4. Stop the reaction by adding SDS-PAGE sample buffer and boil the sample for 10 min.
5. Load samples onto SDS-PAGE gel for immunoblotting analysis.
6. Detect ubiquitin and the target protein with respective antibodies.