Purification of GST-fusion proteins: Difference between revisions

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{{Protokoll-Mix|titel=Materials|Inhalt=LB-Medium 10g Bacto-Trypton, 5g yeast extract, 5g NaCl, pH 7.0, ad 1l A.bidest
{{Protokoll-Mix|titel=Materials|Inhalt=<pre>
Ampicillin 100µg/ml
LB-Medium           10g Bacto-Trypton, 5g yeast extract, 5g NaCl, pH 7.0,
IPTG 100mM Isopropylthiogalactosid
                    ad 1l A.bidest
T-buffer 100mM Tris (pH 8.0), 5mM EDTA
Ampicillin         100μg/ml
Lysis buffer (200 ml): 10 ml Tris pH 8.0 [1M] 50 mM
IPTG               100mM Isopropylthiogalactosid
4 ml EDTA [0.5 M] 10 mM
T-buffer           100mM Tris (pH 8.0), 5mM EDTA
30 ml NaCl [1M] 150 mM
Lysis buffer (200 ml): 10 ml Tris pH 8.0 [1M]     →  50 mM
40 ml Glycerol [50 %] 10 %
                      4   ml EDTA [0.5 M]         →  10 mM
0.5 ml Triton [10 %] 0.025 %
                      30 ml NaCl [1M]             →  150 mM
add freshly à 20 ml:
                      40 ml Glycerol [50 %]       →  10 %
50 µl DTT [1M] 2.5 mM
                      0.5 ml Triton [10 %]         → 0.025 %
20 µl PMSF [10 mg/ml]
                    add freshly à 20 ml:
20 µl Leupeptin [10 mg/ml]
                      50 μl  DTT [1M]             → 2.5 mM
20 µl Aprotenin [10 mg/ml]
                      20 μl  PMSF [10 mg/ml]
20 µl Pefablock [10 mg/ml]
                      20 μl  Leupeptin [10 mg/ml]
Lysozyme 1 mg/ml
                      20 μl  Aprotinin [10 mg/ml]
Sepharose- solution. Glutathione-sepharose-solution
                      20 μl  Pefablock [10 mg/ml]
PBS (1x) 24g NaCl, 0.6g KCl, 3.45g Na2HPO4 x 7 H2O, 0.6 g
Lysozyme             1 mg/ml
KH2PO4, pH 7.4, ad 1l mit A.bidest.}}
Sepharose- solution,
Glutathione-sepharose-solution
PBS (1x)             24g NaCl, 0.6g KCl, 3.45g Na₂HPO₄ x 7 H₂O, 0.6 g
                    KH₂PO₄, pH 7.4, ad 1l mit A.bidest.
</pre>}}


== Procedure ==
== Procedure ==

Revision as of 14:03, 5 June 2025

Materials
LB-Medium           10g Bacto-Trypton, 5g yeast extract, 5g NaCl, pH 7.0,
                    ad 1l A.bidest
Ampicillin          100μg/ml
IPTG                100mM Isopropylthiogalactosid
T-buffer            100mM Tris (pH 8.0), 5mM EDTA
Lysis buffer (200 ml): 10  ml  Tris pH 8.0 [1M]      →   50 mM
                       4   ml  EDTA [0.5 M]          →   10 mM
                       30  ml  NaCl [1M]             →  150 mM
                       40  ml  Glycerol [50 %]       →   10 %
                       0.5 ml  Triton [10 %]         → 0.025 %
                     add freshly à 20 ml:
                       50  μl  DTT [1M]              → 2.5 mM
                       20  μl  PMSF [10 mg/ml]
                       20  μl  Leupeptin [10 mg/ml]
                       20  μl  Aprotinin [10 mg/ml]
                       20  μl  Pefablock [10 mg/ml]
Lysozyme             1 mg/ml
Sepharose- solution,
Glutathione-sepharose-solution
PBS (1x)             24g NaCl, 0.6g KCl, 3.45g Na₂HPO₄ x 7 H₂O, 0.6 g
                     KH₂PO₄, pH 7.4, ad 1l mit A.bidest.

Procedure

The frozen bacteria pellets are thawed in 5 ml T-buffer on ice and resuspended. Afterwards the samples are incubated with 1 ml lysozyme for 30 min. The cells are broken through the addition of 20 ml lysis buffer and the treatment of ultrasonic sound (impulse 50%, 20sec, 3-5x) on ice water.

300 µl sepharose-solution is added to the suspension and incubated for 10 min with head-over-head rotation. Afterwards the lysate is centrifuged for 20 min at 16000 rpm and 4°C. For purification, 1-2 ml 50% glutathione-sepharose solution (GST- Fast4Flow in T-buffer) is added to the lysate, which was washed three times with T- buffer. The sample is then incubated for 2-4 h at 4°C with head-over-head rotation. Afterwards the pellet is washed three times with 1x PBS by centrifugation at 2000 g. The supernatants (wash1-wash3) are collected each time and stored at 4°C. The success of the purification is analysed by SDS-PAGE and Coomassie-staining. The isolated, purified GST-fusion protein coupled to gluthathione-sepharose can now be used for the GST-pulldown. The remaining sample is eluted by the addition of glutathione and is stored at -80°C after dialysis.

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   LB-Medium
   10g Bacto-Trypton, 5g yeast extract, 5g NaCl, pH 7.0,
ad 1l A.bidest
   Ampicillin
   100μg/ml
   IPTG
   100mM Isopropylthiogalactosid
   T-buffer
   100mM Tris (pH 8.0), 5mM EDTA
   Lysis buffer (200 ml):
       10  ml  Tris pH 8.0 [1M]50 mM
4   ml  EDTA [0.5 M]10 mM
30  ml  NaCl [1M]150 mM
40  ml  Glycerol [50 %]10 %
0.5 ml  Triton [10 %]0.025 %
add freshly à 20 ml:
50  μl  DTT [1M]2.5 mM
20  μl  PMSF [10 mg/ml]
20  μl  Leupeptin [10 mg/ml]
20  μl  Aprotinin [10 mg/ml]
20  μl  Pefablock [10 mg/ml]
   Lysozyme
   1 mg/ml
   Sepharose- solution,
Glutathione-sepharose-solution
   PBS (1x)
   24g NaCl, 0.6g KCl, 3.45g Na₂HPO₄ x 7 H₂O, 0.6 g
KH₂PO₄, pH 7.4, ad 1l mit A.bidest.

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