Instructions

Pretreatment: metals can be chelated according to actual needs. After the metal is chelated, use the media according to the following procedures.

Column packing

Column packing should be done according to standard operating procedures. It is important to ensure that each material is at its working temperature, and when possible, the chromatography media may be degassed before column packing.

Equilibration

Equilibrate the column with an appropriate 2-5 column volume buffer. Ensure the conductivity and pH of the effluent are exactly the same as the buffer.

Sample feeding

1. The sample is generally dissolved in the equilibration buffer solution at pH 6-8, and increasing the pH of the loading buffer may increase the protein loading capacity.

2. The buffer should not contain metal chelating agents such as EDTA and citrate, and it is best to avoid reducing agents such as mercaptoethanol and DTT.

3. Commonly used buffers include 10-100 mmol/L sodium phosphate, 20-200 mmol/L Tris-HCl, etc.

4. Generally, 0.15-0.5mol/L NaCl should be added to the buffer to eliminate ion exchange interactions.

5. When using the metal chelating agarose media for the first time, it is recommended to use 50mmol/L PBS (50 mmol/L NaH₂PO₄, 0.5 mol/L NaCl, pH 7.4) as the initial buffer.

Elution

Typically, the following methods can be used for protein elution:

1. Lower pH: most proteins will be eluted at pH 6-4 (also at pH 3-4), the buffer can be sodium acetate, and phosphate buffer systems.

2. Competitive elution: linearly increase or one-step increase the concentration of competing substances with affinity to metal ions (such as 0-1.0 mol/L imidazole, 0-50 mmol/L histidine, 0-2 mol/L NH₄Cl).

3. Chelating agents: Chelating agents such as EDTA and EGTA can bind to metal ions and release the proteins. However, this method cannot separate different proteins and will remove the metal from the resin.

Note:

1. When using for the first time, if the concentration required for elution is not certain, it is recommended to add 10mmol/L, 20mmol/L, 50mmol/L, 100mmol/L, 200mmol/L, 500mmol/L or more imidazole to the initial buffer solution, from low to high concentration, to elute and collect the recombinant proteins respectively, and then identify the elution results by SDS-PAGE electrophoresis and other methods. If conditions permit, linear imidazole gradient elution can be performed to determine better elution conditions.

2. Imidazole is alkaline, and the pH needs to be adjusted using HCl after the corresponding buffer solution is prepared.

3. Elution by lowering pH and with chelating agent will cause the metal ions to be removed from the resin. The metal ions will need to be re-chelated to the resin before the next use.

For all the above elution methods, 150-500mmol/L NaCl should be added to the buffer to eliminate any ion exchange interactions.

Regeneration

1. After multiple uses or when the chelated metal ions need to be replaced, the metal must be stripped of the chromatographic media and the resin regenerated.

Metal removal method: First rinse the column with 5-10 CV of distilled water, then rinse the column with 5-10 CV of 100mmol/L EDTA, and finally use 2-3 CV of 0.5mol/L NaCl to wash off residual EDTA.

2. Columns that have been used many times generally require cleaning after metal removal.

Cleaning method: reverse wash the column with 0.1-1.0 mol/L NaOH, and keep it at 50 cm/h for 1-2 hours, which should remove the strongly bound impurities.

3. Metal ions need to be re-chelated after washing.

Chelating method: First, use 2-5 CV of distilled water to fully balance the column after previous metal removal, then use 0.1-0.3mol/L metal salt solution (chloride or sulfate soluble metal salts are suitable) to pass through the column for 5-10 CV to chelate the fresh metal ions, and finally use 5-10 CV of distilled water to remove unbound metal ions.

Cleaning-In-Place (CIP)

1. Removal of proteins adsorbed by ion exchange: first use 2 mol/L NaCl solution to backwash 2 to 3 CV, then rinse with 3 to 5 CV with distilled water.

2. Removal of precipitated proteins, hydrophobic proteins and lipids: first use 1.0 mol/L NaOH to backwash the column (50 cm/h, contact time 1-2 h), contact for more than 12 hours to remove endotoxin. Then rinse the chromatography column with 10 CV of equilibration buffer, and finally rinse the chromatography column with 5 CV of distilled water.

3. Removal of hydrophobic proteins and lipids: first wash the chromatography column with 5-10 CV of 30% isopropanol in reverse phase (contact time 15-20min), then rinse the chromatography with 10 CV of distilled water column.

Storage

Sealed and stored at 4~30°C (preservation solution is 20% ethanol) in a ventilated, dry and clean place, do not freeze. 

Ordering information

Production date: See label

Expiry date: 5 years, under proper storage conditions

Manufacturer: Sunresin New Materials Co. Ltd.

Add:No. 135, Jinye Rd, Xi'an 

Hi-Tech Industrial Development Zone, Shaanxi, 710076, China

www.seplite.com    www.sunresin.com

E-mail: info.lifescience@sunresin.com