Sauer:ClpP purification/Untagged ClpP

Buffers

Buffer L: 50 mM Tris-HCl (pH 7.6), 1 mM DTT, 0.5 mM EDTA, 10% Glycerol

Buffer L150: Buffer L + 150 mM KCl

Buffer L400: Buffer L + 400 mM KCl

Buffer L100: Buffer L + 100 mM KCl

Protocol

1. Suspend cells expressing ClpP in 10mL/L culture of Buffer L150.

2. Freeze at -80°C until use.

3. Thaw by addition of 10mL/L culture Buffer L150.

4. Add 1 mg/mL lysozyme, and let sit in ice, ~1 hour.

5. Sonicate to reduce viscosity. (or use DNase or Benzonase, they need Mg++ and Ca++)

6. Spin at 15K rpm in a SA-600 rotor, 30’.

7. Add AmSO₄ to 30% saturation (0.164 g/mL) while gently stirring on ice and incubate on ice for 30’.

8. Spin at 10K rpm, 15’; save supernatant.

9. Add to AmSO₄ to 60% saturation (0.181 g/mL) while stirring on ice and incubate on ice 30’.

10. Spin at 10K rpm, 15’; save pellet.

11. Resuspend pellet in Buffer L150 (I used 5 mL per 1L culture but this was more than I needed:Marylee)

12. Desalt into a PD-10 column (with fresh Buffer L150) or decrease conductivity by dilution into L150.

13. HiLoad 16/10 Q Sepharose HP separation. The mobile phase contains Buffer L150 and elution proceeds with a 200 mL linear gradient between 150mM and 400 mM KCl.

14. Concentrate sample by precipitation in 60% AmSO₄, and then incubate at 4°C, 30’.

15. Spin at 10K rpm and resuspend in Buffer L100.

16. Gel filtration using a HiPrep Sephacryl S-300HR column in Buffer L100.

17. Concentrate fractions on a HiLoad 16/10 Q Sepharose column or by a spin concentrator.