Materials and Reagents

35 mm TC-treated culture dish (Corning, catalog number: 430165 )
Razor blades
Protein purification column (Kimble Chase Life Science and Research Products, catalog number: 420400-1010 )
Pipette tips (VWR, catalog number: 53508-794 )
50 ml tube (Corning, catalog number: 430290 )
VWR 10 ml serological pipet (VWR, catalog number: 89130-888 )
Parafilm M (Bemis, catalog number: PM996 )
Immobilon-P polyvinylidene difluoride membrane (EMD Millipore, catalog number: IPVH00010 )
Dialysis tube (Sigma-Aldrich, catalog number: D6191 )
Dialysis tube clip (Sigma-Aldrich, catalog number: Z371092 )
Dialysis tubing (Sigma-Aldrich, catalog number: D9652 )
pGEM^®-T Easy vector systems (Promega, catalog number: A1360 )
One Shot TOP10 competent cells (Thermo Fisher Scientific, Invitrogen^TM, catalog number: C404003 )
pET-28a(+) plasmid (EMD Millipore, catalog number: 69864 )
DMEM (Thermo Fisher Scientific, Gibco^TM, catalog number: 11965092 )
FBS (Thermo Fisher Scientific, Gibco^TM, catalog number: 10437028 )
Penicillin-streptomycin (10,000 U/ml) (Thermo Fisher Scientific, Gibco^TM, catalog number: 15140122 )
TRIzol reagent (Thermo Fisher Scientific, Ambion^TM, catalog number: 15596026 )
Chloroform, biotechnology grade (VWR, catalog number: 97064-678 )
2-propanol, biotechnology grade (VWR, catalog number: 97065-048 )
Ethanol, absolute (Sigma-Aldrich, catalog number: E7023 )
DEPC-treated water (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 750023 )
5x iScript cDNA Synthesis Kit (Bio-Rad Laboratories, catalog number: 1708890 )
Nuclease-free water (New England Biolabs, catalog number: B1500 )
PCR primers (IDT)
Phusion high-fidelity DNA polymerase (New England Biolabs, catalog number: M0530 )
dNTP (New England Biolabs, catalog number: N0447 )
Taq DNA polymerase (New England Biolabs, catalog number: M0273 )
Magnesium chloride (MgCl₂) solution (New England Biolabs, catalog number: B9021 )
dATP (100 mM) (New England Biolabs, catalog number: N0440S )
T4 DNA ligase (New England Biolabs, catalog number: M0202 )
X-Gal (β-galactoside) (Promega, catalog number: V3941 )
SOC medium (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 15544034 )
LB plate (Thermo Fisher Scientific, Gibco^TM, catalog number: 10855021 )
Ampicillin (Sigma-Aldrich, catalog number: A9393 )
NEBuffer 3.1 (New England Biolabs, catalog number: B7203S )
SalI restriction enzyme (New England Biolabs, catalog number: R0138 )
NotI restriction enzyme (New England Biolabs, catalog number: R0189 )
Qiagen QIAquick Gel Extraction Kit (QIAGEN, catalog number: 28706 )
T4 DNA ligase buffer (New England Biolabs, catalog number: B0202S )
IPTG (Sigma-Aldrich, catalog number: I6758 )
Liquid nitrogen (Midwest Liquid Nitrogen Service)
Lysozyme (Sigma-Aldrich, catalog number: L6876 )
RNase A (Sigma-Aldrich, catalog number: R4642 )
DNase I (New England Biolabs, catalog number: M0303 )
LDS loading buffer (4x) (Thermo Fisher Scientific, Noves^TM, catalog number: NP0007 )
Ni-NTA agarose (QIAGEN, catalog number: 30230 )
Qubit Protein Assay (Thermo Fisher Scientific, Molecular Probes^TM, catalog number: Q33211 )
λ-PPase (New England Biolabs, catalog number: P0753 )
Phosphatase reaction buffer (New England Biolabs, catalog number: B6022S )
Sodium orthovanadate (Sigma-Aldrich, catalog number: S6508 )
Poly I:C (Sigma-Aldrich, catalog number: P1530 )
NuPAGE 4-12% Bis-Tris protein gel (Thermo Fisher Scientific, Invitrogen^TM, catalog number: NP0322BOX )
Silver staining kit (Thermo Fisher Scientific, Noves^TM, catalog number: LC6100 )
1% bovine serum albumin (BSA) (Sigma-Aldrich, catalog number: A9418 )
PKR primary antibody (Santa Cruz Biotechnology, catalog number: sc-6282 )
Phosphorylated-PKR primary antibody (Abcam, catalog number: ab32036 )
Peroxidase-conjugated secondary antibody (Thermo Fisher Scientific, Invitrogen^TM, catalog number: 31460 )
ECL reagents (Thermo Fisher Scientific, Thermo Scientific^TM, catalog number: 32132 )
Sodium phosphate monobasic (NaH₂PO₄) (Sigma-Aldrich, catalog number: S8282 )
Sodium chloride (NaCl) (Sigma-Aldrich, catalog number: S7653 )
Imidazole (Sigma-Aldrich, catalog number: I5513 )
PMSF (Sigma-Aldrich, catalog number: P7626 )
Protease inhibitor (Roche Diagnostics, catalog number: 11697498001 )
Sodium hydroxide (NaOH) (Sigma-Aldrich, catalog number: S8045 )
Tris (pH 7.6) (VWR, catalog number: 97061-260 )
Potassium chloride (KCl) (Sigma-Aldrich, catalog number: P9333 )
Magnesium chloride (MgCl₂) powder (Sigma-Aldrich, catalog number: M8266 )
Glycerol (VWR, BDH^®, catalog number: BDH1172-1LP )
EDTA (Sigma-Aldrich, catalog number: E6758 )
DTT (Sigma-Aldrich, catalog number: D0632 )
HEPES (pH 7.5) (Sigma-Aldrich, catalog number: H3375 )
ATP (New England Biolabs, catalog number: P0756 )
Potassium phosphate monobasic (KH₂PO₄) (Sigma-Aldrich, catalog number: P5655 )
Tween-20 (Sigma-Aldrich, catalog number: P9416 )
E. coli lysis buffer (see Recipes)
Protein purification wash buffer (see Recipes)
Protein purification elution buffer (see Recipes)
Protein storage buffer (see Recipes)
Phosphatase reaction buffer (see Recipes)
PKR activation buffer (see Recipes)
TE buffer (10x) (see Recipes)
Tween-20 phosphate buffered saline (pH 7.2) (see Recipes)

Equipment

Cell culture incubator (Panasonic Biomedical, model: MCO-230AIC )
Pipette (VWR, catalog number: 89079-970 )
Centrifuge (Eppendorf, model: 5424 )
Qubit 3.0 Fluorometer (Thermo Fisher Scientific, Invitrogen^TM, catalog number: Q33216 )
PCR machine (Bio-Rad Laboratories, model: S1000^TM Thermal Cycler , catalog number: 1852148)
Vortex (VWR, catalog number: 97043-562 )
Sonicator (Branson, model: Digital Sonifier 450 or from Fisher Scientific, catalog number: 15-338-553)
600 ml beaker (VWR, catalog number: 10754-956 )
Typhoon scanner (GE Healthcare, model: Amersham Molecular Dynamics Typhoon 9410 or from GMI, catalog number: 8149-30-9410)

Procedure

Human PKR gene cloning
1. RNA isolation and cDNA library generation
  1. Grow the cells in a 35 mm dish with 10 ml DMEM with 10% FBS and 1% penicillin-streptomycin in a 37 °C incubator with 5% CO₂ until 80% confluence.
  2. Remove the media from the culture dish.
  3. Add 1 ml TRIzol reagent directly to the cells in the culture dish.
  4. Pipette the cells up and down for 5 times in the culture dish to lyse the cells.
  5. Incubate the sample at room temperature for 5 min to allow for complete nuclear lysis.
  6. Add 0.2 ml of chloroform and share the tube vigorously by hand for 15 sec.
  7. Incubate for 2 min at room temperature.
  8. Centrifuge the sample at 12,000 x g for 15 min at 4 °C.
  9. Remove the aqueous supernatant by angling the tube at 45° to avoid contacting the interphase or the organic layer.
  10. Transfer the aqueous phase into a new tube and add 0.5 ml of 100% isopropanol.
  11. Incubate at room temperature for 10 min.
  12. Centrifuge at 12,000 x g for 10 min at 4 °C.
    Note: RNA should be visible as a white pellet.
  13. Remove the supernatant carefully from the tube without touching the RNA pellet.
  14. Wash the pellet with 1 ml of 75% ethanol pre-chilled at 4 °C.
  15. Vortex the sample briefly, followed by centrifugation at 7,600 x g for 5 min at 4 °C.
  16. Remove the ethanol carefully and air dry the RNA pellet for 15 min on ice.
  17. Re-suspend the RNA pellet in 100 μl DEPC-treated water and incubate at 37 °C for 10 min.
  18. Measure the RNA concentration using a Qubit 3.0 Fluorometer, NanoDrop spectrophotometer or Bioanalyzer.
  19. Prepare the 5x iScript cDNA Synthesis reaction mix on ice for reverse transcription.
  20. Incubate the reaction mix on a PCR machine with the following program:
    5 min at 25 °C
    30 min at 42 °C
    5 min at 85 °C
    Hold at 4 °C
  21. Store the cDNA in aliquots at -20 °C. Alternatively, store the cDNA at 4 °C if used repeatedly in days. Avoid repeated freezing and thawing cycles.
2. PCR amplification and subcloning into pET-28a+ plasmid
  Other bacterial expression plasmids may be used. Different restriction enzymes may be used in other plasmids depending on the cloning sites.
3. Transformation into E. coli
4. Digestion and ligation of PKR gene into pET-28a+
PKR protein purification from E. coli
1. Grow the cells in LB broth at 37 °C until OD₆₀₀ reaches 0.4-0.6.
2. Induce with 40 µl of a 100 mM IPTG (final concentration 400 µM) for 3 to 5 h at 37 °C.
3. Harvest the cells and proceed immediately to cell lysis or freeze the cells in liquid nitrogen followed by storing them at -80 °C.
4. Resuspend the cells in lysis buffer at 2-5 ml per gram wet weight.
5. Add lysozyme (1 mg/ml) to the lysis buffer with the cells and incubate on ice for 30 min.
6. Sonicate on ice using a sonicator equipped with a microtip.
  Note: Use five 15 sec bursts at 30x with a 45 sec cooling period between each burst.
7. (Optional) If the lysate is very viscous, add RNase A (10 μg/ml) and DNase I (5 μg/ml) and incubate on ice for 10-15 min.
8. Centrifuge lysate at 10,000 x g for 20-30 min at 4 °C to pellet the cellular debris and keep the supernatant.
9. Add 5 μl 2x LDS-PAGE sample buffer to 5 μl supernatant and store at -20 °C for LDS-PAGE analysis.
10. Pipette 10 ml of Ni-NTA slurry to a 50 ml tube and briefly centrifuge. Remove supernatant and add 20 ml of lysis buffer. Mix gently by inverting. Repeat centrifugation step and remove the supernatant.
  Note: Adjust the amount of Ni-NTA used depending on the yield of the target protein.
11. Add cleared lysate to this equilibrated matrix and mix gently by shaking at 4 °C for 1 h.
12. Load 10 ml lysate-Ni-NTA mixture into a column.
13. Remove bottom cap and collect the flow-through. Save and store for Western blotting.
14. Wash 10 times with wash buffer. Collect wash factions for Western blotting.
15. Elute protein 4 times with 1 ml elution buffer.
16. Perform dialysis in storage buffer overnight at 4 °C.
17. Wet the dialysis tube with distilled water and close the tube with a clip near one end.
18. Load the sample into the dialysis tube and clip another end.
19. Immerse the knotted tube in storage buffer in a 500 ml beaker overnight.
20. Measure protein concentration by Qubit Protein Assay and check the purity of protein (Figure 1).
  
  Figure 1. Silver staining of purified PKR protein. The purified PKR protein (65 kDa) was visualized by silver staining. IPTG was added to induce the protein expression in E. coli. Lysate from cells without IPTG induction was used as a negative control.
PKR dephosphorylation and activation
Human PKR protein is activated by the RNAs from E. coli upon cell lysis; therefore, protein dephosphorylation is necessary to obtain the non-phosphorylated form of PKR before activation assays.
1. Dephosphorylation of PKR
2. In vitro PKR activation assay

Data analysis

All experiments were repeated independently at least in triplicate, and the data are presented as mean ± SD. Statistical significance was determined using the Student’s t-test. A P value of < 0.05 was considered to be statistically significant. The experiments described in this protocol has been performed and their data have been published in Yuen et al., 2016, NIPBL controls RNA biogenesis to prevent activation of the stress kinase PKR. Cell Rep 14(1): 93-102, which can be accessed by: http://www.cell.com/cell-reports/fulltext/S2211-1247(15)01425-4.

Recipes

E. coli lysis buffer (1 L)
50 mM NaH₂PO₄
300 mM NaCl
10 mM imidazole
1 mM PMSF
10 mM protease inhibitor
Adjust pH to 8.0 using NaOH
Protein purification wash buffer (1 L)
50 mM NaH₂PO₄
300 mM NaCl
20 mM imidazole
1 mM PMSF
10 mM protease inhibitor
Adjust pH to 8.0 using NaOH
Protein purification elution buffer (1 L)
50 mM NaH₂PO₄
300 mM NaCl
250 mM imidazole
1 mM PMSF
10 mM protease inhibitor
Adjust pH to 8.0 using NaOH
Protein storage buffer
10 mM Tris (pH 7.6)
50 mM KCl
2 mM MgCl₂
10% glycerol
7 mM β-mercaptoethanol
Phosphatase reaction buffer
50 mM Tris-HCl, pH 7.5
2 mM MgCl2
0.1 mM EDTA
5 mM DTT
PKR activation buffer
20 mM HEPES (pH 7.5)
4 mM MgCl₂
100 mM KCl
1 mM ATP
TE buffer (10x)
100 mM Tris-Cl
10 mM EDTA (pH 8.0)
Tween-20 phosphate buffered saline (pH 7.2) (1 L)
8 g of NaCl
0.2 g of KCl
1.44 g of Na₂HPO₄
0.24 g of KH₂PO₄
2 ml of Tween-20

Acknowledgments

I would like to thank Dr. Jennifer Gerton for reading this protocol. This study was supported by Stowers Institute for Medical Research, the Cornelia de Lange Syndrome (CdLS) Foundation, and the March of Dimes (MOD) Foundation (6-FY14-434).

References

Bevilacqua, P. C., George, C. X., Samuel, C. E. and Cech, T. R. (1998). Binding of the protein kinase PKR to RNAs with secondary structure defects: role of the tandem A-G mismatch and noncontiguous helixes. Biochemistry 37(18): 6303-6316.
Hinnebusch, A. G. (2005). eIF2α kinases provide a new solution to the puzzle of substrate specificity. Nat Struct Mol Biol 12(10): 835-838.
Holcik, M. and Sonenberg, N. (2005). Translational control in stress and apoptosis. Nat Rev Mol Cell Biol 6(4): 318-327.
Manche, L., Green, S. R., Schmedt, C. and Mathews, M. B. (1992). Interactions between double-stranded RNA regulators and the protein kinase DAI. Mol Cell Boil 12(11): 5238-5248.
Nallagatla, S. R. and Bevilacqua, P. C. (2008). Nucleoside modifications modulate activation of the protein kinase PKR in an RNA structure-specific manner. RNA 14(6): 1201-1213.
Yuen, K. C., Xu, B., Krantz, I. D. and Gerton, J. L. (2016). NIPBL controls RNA biogenesis to prevent activation of the stress kinase PKR. Cell Rep 14(1): 93-102.
Zheng, X. and Bevilacqua, P. C. (2004). Activation of the protein kinase PKR by short double-stranded RNAs with single-stranded tails. RNA 10(12): 1934-1945.