Purification of GST fusion proteins in E.coli GST融合蛋白纯化，方法一

Making GST fusion proteins:(07/19/03)ver.1

Grow up 5ml LB with Amp o/n.

Add to 45ml LB with Amp

37o shake 2.5 - 3 hrs,till OD₆₀₀ 0.4-0.8

Put bottles in room temperature water for 10 min to cool down.

Add 100μl 0.2M IPTG to 0.4mM final

Shake 30℃ 2hr

Pellet bacteria,decant sup,invert to drain

Resuspend in 1ml NETN 0.2mM PMSF / 50ml LB

PMSF,stock 10mM

NETN: 20mM Tris-Cl (pH8)

100mM NaCl

1mM EDTA

0.5% NP40

store at 4℃

Vortex to mix well

Sonicate at scale 5 for 15sec.Keep on ice.For 10ml Corning tubes,use scale 7

Spin 4℃,5min

Transfer supernatant to a new tube.

To each lysate,add 60μl 50% Glutathione-Sepharose 4B

Pepette 400μl Sepharose stock (75%)

Spin 1000rpm 5min,discard supernantant

Wash 3x300μl NETN

Resuspend in 300μl NETN to get 50% beads

Mix in cold room for 2 hours,slowly whirl

Pellet beads by brief centrifugation,carefully discard supernatant

Wash 3x1ml NETN/PMSF

Wash 2x1ml Elution Buffer (50mM Hepes,pH7.9,40mM KCl,1mM EDTA 1mM DTT)

Elute proteins by mix beads with 60μl each

Elution buffer

5mM Glutathione,(for 10mM,use 3.07mg/ml)

1mM DTT

Slowly swirl at RT 1hr

Quick spin to pellet,transfer supernatant to a new tube

Re-elute with 60μl each

NETN

5mM Glutathione

1mM DTT

Slowly swirl at RT 30min

Quick spin,combine supernatant,spin and transfer supernatant twice to avoid any residual beads.total is 120μl now.

Dialyze vs 50% glycerol/10mM Hepes,pH7.5/ 40mM KCl/ 1mM EDTA/ 1mM DTT/ 1mM PMSF in cold room for 2hr or o/n,store at -20℃

Proteins can also be concentrated in a Centriprep-30 concentrator.The pore size of the membrane in the Centriprep-30 allows glutathione to pass into the aqueous compartment.PBS can be added to the protein concentrate and the concentration procedure can be repeated.

Thinking aliquot and save at -80℃

Run 12% SDS-PAGE