Difference between revisions of "Purification of GST Fusion Proteins"
From Bridges Lab Protocols
m (Updates to previous version, updatite the lysis and purification section.) |
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==Bacteria Production and Induction== | ==Bacteria Production and Induction== | ||
| − | + | *Express and induce protein in culture under appropriate conditions: | |
| − | #grow an overnight culture in ~25 mL LB/Amp ( | + | #grow an overnight culture in ~25 mL LB/Amp (with Chloramphenicol if using Rosetta cells) from a colony <2 weeks post transformation. |
| − | #add 5 mL culture to 1L TB/Amp and grow at 37C | + | #add 5 mL overnight culture to 1L TB/Amp and grow at 37C |
| − | #grow to OD600 of 0.6-1.0 and induce with | + | #grow to OD600 of 0.6-1.0 and induce with 100 uM IPTG (the concentration of IPTG and duration of induction should be optimized for each protein) |
#let grow O/N at <25C (optimize induction time/temp for each protein, see [[Induction Conditions]]). | #let grow O/N at <25C (optimize induction time/temp for each protein, see [[Induction Conditions]]). | ||
| − | #centrifuge cells 10 min at 9000 RPM to pellet bacteria freeze if stopping at this point | + | #centrifuge cells 10 min at 9000 RPM to pellet bacteria freeze if stopping at this point. |
| + | |||
==Lysis and Purification== | ==Lysis and Purification== | ||
#Resuspend cells in ~20 mL lysis buffer (PBS + 0.1% B-ME and a PI tablet). Freeze in liquid nitrogen if not continuing with purification | #Resuspend cells in ~20 mL lysis buffer (PBS + 0.1% B-ME and a PI tablet). Freeze in liquid nitrogen if not continuing with purification | ||
Revision as of 14:34, 12 August 2009
Bacteria Production and Induction
- Express and induce protein in culture under appropriate conditions:
- grow an overnight culture in ~25 mL LB/Amp (with Chloramphenicol if using Rosetta cells) from a colony <2 weeks post transformation.
- add 5 mL overnight culture to 1L TB/Amp and grow at 37C
- grow to OD600 of 0.6-1.0 and induce with 100 uM IPTG (the concentration of IPTG and duration of induction should be optimized for each protein)
- let grow O/N at <25C (optimize induction time/temp for each protein, see Induction Conditions).
- centrifuge cells 10 min at 9000 RPM to pellet bacteria freeze if stopping at this point.
Lysis and Purification
- Resuspend cells in ~20 mL lysis buffer (PBS + 0.1% B-ME and a PI tablet). Freeze in liquid nitrogen if not continuing with purification
- French Press cells 2 x 15 000 psi (see French Press Protocol)
- Centrifuge lysate at >15 000 RPM (i.e. 20,000RMP in JA25.5 at 4 degrees C) for 30 min to clarify
- Add 1.0 mL glutathione-agarose to 50 mL PBS (no PI) to prepare beads. Let sit for 30 min. to allow beads to settle or pellet beads for 5 min at 1000 RPM and remove buffer
- Save a lysate sample (20 uL) and add clarified lysate to equilibrated beads
- Incubate with rotation for 1h at 4C
- Pellet beads (save sample of unbound protein) and wash 3 x 50 mL cold wash buffer being careful to not suck up beads
- Pour into disposable column (BioRad # 732-6008) to collect beads. Wash with another 10 mL of PBS
- Elute with ~5 mL room temp. elution buffer, collecting 10 x ~0.5 mL fractions. Check fractions for protein with Bradford assay
- Elution buffer contains 50mM Glutathionie in PBS(0.615g in 40mL PBS), pH to between 7 and 8.
- Combine fractions with protein and dialyse O/N into 200 mL PBS in 50% glycerol (will concentrate sample ~4X)
- Measure protein concentration (Bradford or A280; concentrate if necessary and store at -20)
- Analyze uninduced and induced cells (0.5 mL culture resuspended in 100 uL 2X SDS), lysate (5 uL in 2X), unbound (5 uL in 2X) and protein (0.5-10 ug) by SDS-PAGE
