2 users have reported that they have successfully carried out the experiment using this protocol.

Purification of Adenovirus by Cesium Chloride Density Gradients   

Abstract

Materials and Reagents

1. HEK293 cell
   
2. Glycerol
   
3. Liquid nitrogen
   
4. 70% ethanol
   
5. Distilled water
   
6. SDS
   
7. CaCl₂
   
8. MgCl₂
   
9. CsCl₂ (Thermo Fisher Scientific, catalog number: BP1595-500 )
   
10. Tris-HCl (pH 8.0)
    
11. TE
    
12. EDTA
    
13. SDS
    
14. Sucrose
    
15. 5% deoxycholate (see Recipes)
    
16. Dialysis buffer (see Recipes)
    
17. Balance buffer (see Recipes)
    
18. Saturated CsCl₂ (see Recipes)
    

Equipment

1. Centrifuges
   
2. Ultracentrifuge
   
3. Laminar flow hood
   
4. Syringe
   
5. Water bath
   
6. Slide-A-Lyzer 10 K dialysis cassette (Thermo Fisher Scientific, catalog number: 66203 )
   
7. Spectrometer
   
8. Ti50.2 tube
   

Procedure

1. Thaw HEK293 cell suspension (with adenovirus in TE +5% glycerol 20.5 ml) from liquid nitrogen at 37 °C.
   
2. Add 1.23 ml 5% deoxycholate to 0.3% final concentration and vortex.
   
3. Incubate on ice for 30 min (vortex every 10 min). During incubation, prepare homoginizer: wash with 70% ethanol, then with distilled water, then sterilize under ultraviolet light.
   
4. Homoginize until cell suspension becomes free flowing (set to 25, three times, 2 min for homogenization and 3 min on ice each time).
   Wash homogenizer: 1x 1% SDS, 5x regular water, 3x sterilized dH₂O, dry up.
   
5. Incubate cell suspension on ice for 15 min (vortex each 5 min).
   
6. Spin 30 min at 9,000 x g to remove cell debris on 4 °C.
   
7. Load 11.9 ml of saturated CaCl₂ and 20.5 ml of the homogenate onto an ultracentrifuge tube (fit to Ti50.2 tube).
   
8. Place a cap on to the ultracentrifuge tube. Do not introduce any air bubbles and mix well.
   
9. Load the other balanced buffer tube, place cap and avoid bubbles. Weigh two ultracentrifuge tubes. If there is over 0.05 g difference in weight, adjust the balanced tube with TE or CsCl₂.
   
10. Ultracentrifuge 35,000 rpm for 20 h at 4 °C. After that, you will see a viral particle band.
    
11. In a laminar flow hood, carefully remove the tubes from the rotor, then open the cap.
    
12. Using a 1 ml syringe with a 23 G1 needle, puncture the side of tube below the viral particle band (cloudy white).
    
13. Aspirate the viral band (about 1 ml) carefully, avoid collecting other bands and impurities. If the viral band is over 1 ml, use another 1 ml syringe with 23 G1 needle and puncture at different position of tube to collect virus.
    
14. Transfer virus directly to a Slide-A-Lyzer 10 K dialysis cassette that should be hydrated by immersing into dialysis buffer for 30 min.
    
15. Insert the tip of the needle at a top corner of the cassette, and inject virus slowly.
    
16. Transfer the virus cassette into an autoclaved 1 L baker containing 1,000 ml dialysis buffer with the lowest speed of stir bar spin.
    
17. Dialyze at 4 °C for 2 h then change fresh buffer and dialyze overnight. On the second day, change 1,000 ml fresh buffer and dialyze for another 4 h.
    
18. Carefully collect the virus by sucking with syringe to a clean sterilized tube, measure OD₂₆₀ with 1:50 dilution.
    
19. Calculate virus concentration (VP/ml): OD₂₆₀ x 50 x 10¹⁰. Aliquot, store at -80 °C.
    

Recipes

1. TE
   10 mM Tris-HCl (pH 8.0)
   1 mM EDTA
   
2. Saturated CsCl₂
   Add CsCl₂ 25 g to TE, and stir, repeat the addition until CsCl₂ doesn’t dissolve anymore. Transfer the solution to 37 °C water bath, add more CsCl₂. It takes about 100 g CsCl₂ to saturate 50 ml buffer. Autoclave and store at RT.
   
3. 5% deoxycholate
   5% deoxycholate in water, filter sterilized.
   
4. 1% SDS (for washing the probe), filter sterilized.
   
5. Balance buffer (10 ml)
   6.4 ml TE and 3.6 ml of saturated CsCl₂
   
6. Dializing buffer (4 L)
   10 mM Tris (pH 8.0)
   2 mM MgCl₂
   5% sucrose
   

References

1. Duffy, A. M., O'Doherty, A. M., O'Brien, T. and Strappe, P. M. (2005). Purification of adenovirus and adeno-associated virus: comparison of novel membrane-based technology to conventional techniques. Gene Ther 12 Suppl 1: S62-72.
   
2. Graham, F. L. and Prevec, L. (1991). Manipulation of adenovirus vectors. Methods Mol Biol 7: 109-128.
   
3. Guo, Z., Su, W., Ma, Z., Smith, G. M. and Gong, M. C. (2003). Ca²⁺-independent phospholipase A2 is required for agonist-induced Ca²⁺ sensitization of contraction in vascular smooth muscle. J Biol Chem 278(3): 1856-1863.