Performing a Separation with Cytiva Products Based on GST Fusion Proteins

* See Appendix 4 to convert linear flow (cm/h) to volumetric flow rate. Maximum operating flow is calculated from measurement in a packed column with a bed height of 10 cm and i.d. of 5 cm.

Purification Examples

Figure 22 shows a typical purification of GST fusion protein on GSTrap FF 1 ml with an SDS-PAGE analysis of the purified protein.

Figure 23 shows how the purification of a GST fusion protein can be scaled up 20-fold from a GSTrap FF 1 ml column to a GSTPrep FF 16/10 column.

Performing a Separation

Binding buffer: 140 mM NaCl, 2.7 mM KCl, 10 mM Na₂HPO₄, 1.8 mM KH₂PO₄, pH 7.3

Elution buffer: 50 mM Tris-HCl, 10 mM reduced glutathione, pH 8.0

1. Equilibrate the column with 5 column volumes of binding buffer.
2. Apply the sample.
3. Wash with 5–10 column volumes of binding buffer.
4. Elute with 5–10 column volumes of elution buffer.
5. Wash with 5–10 column volumes of binding buffer.

It is important to keep a low flow rate during sample loading and elution as the kinetics of the binding interaction between GST and glutathione are relatively slow. The binding capacity is protein dependent and therefore yield will vary according to the type of protein. Yield may be improved by using a slower flow rate or passing the sample through the column several times.

For a single purification of a small quantity of product or for high throughput screening, GST MicroSpin columns are convenient and simple to use with either centrifugation or MicroPlex 24 Vacuum.

To increase capacity, connect several GSTrap FF columns (1 ml or 5 ml) in series. For greater capacity, use GSTPrep 16/10 FF columns or pack Glutathione Sepharose 4 Fast Flow into a suitable column (see Appendix 3, Column packing and preparation for affinity chromatography). GSTrap FF columns can be used with a syringe, a peristaltic pump or a chromatography system.

Enzyme-specific recognition sites are often included to allow the removal of the GST tag by enzymatic cleavage when required. Thrombin is commonly used for enzymatic cleavage, and must, subsequently, be removed from the recombinant product. HiTrap Benzamidine FF (high sub) 1 ml or 5 ml columns provide simple, ready-made solutions for this process (see page 54, Purifcation or removal of serine proteases, e.g. thrombin and trypsin, and zymogens).

Reuse of GSTrap FF depends on the nature of the sample. To prevent cross-contamination, columns should only be reused with identical samples.

Cleaning

These procedures are applicable to Glutathione Sepharose 4 Fast Flow and Glutathione Sepharose 4B.

1. Wash with 2–3 column volumes of alternating high pH (0.1 M Tris-HCl, 0.5 M NaCl, pH 8.5) and low pH (0.1 M sodium acetate, 0.5 M NaCl, pH 4.5) buffers.
2. Repeat the cycle 3 times.
3. Re-equilibrate immediately with 3–5 column volumes of binding buffer.

If the medium is losing binding capacity, this may be due to an accumulation of precipitated, denatured or non-specifically bound proteins.

To remove precipitated or denatured substances:

1. Wash with 2 column volumes of 6 M guanidine hydrochloride.
2. Wash immediately with 5 column volumes of binding buffer.

To remove hydrophobically bound substances:

1. Wash with 3–4 column volumes of 70% ethanol (or 2 column volumes of a non-ionic detergent (Triton™ X-100 1%)).
2. Wash immediately with 5 column volumes of binding buffer.

Chemical Stability

No significant loss of binding capacity when exposed to 0.1 M citrate (pH 4.0), 0.1 M NaOH, 70% ethanol or 6 M guanidine hydrochloride for 2 hours at room temperature. No significant loss of binding capacity after exposure to 1% SDS for 14 days.

Storage

Wash media and columns with 20% ethanol at neutral pH (use approximately 5 column volumes for packed media) and store at +4 to +8 °C.