- to purify filtered protein through FPLC and
- to remake Au/BSA solutions to run through Atomic Absorption.
Purifying Protein via FPLC
- The FPLC column was washed with 100mL binding buffer (pH 7.5 with Tris, NaCl, and 30mM of imidazol).
- The filtered protein supernatant from yesterday was injected into the column.
- The flow through from the column was collected in the same 50ml falcon tube that previously contained the protein supernatant as a precaution in case protein failed to bind to column.
- 200mL elution buffer was pushed through the column while collecting the binded ADA protein in 5mL aliquots in separate test tubes.
- NOTE: The nickel column binds to the histidine complex of Adenosine Deaminase (ADA) protein. Adenosine Deaminase is the only protein among protein supernatant with histidine complex. So theoretically, the ADA protein will be the only protein that sticks to the nickel column. The elusion buffer contains a high concentration of imidazole that competes with the nickel to bind to the histidine of the ADA protein. Theoretically, the ADA protein will be more attracted to the imidazole in the elusion buffer than the nickel in the column. Therefore, the ADA protein would flow through the column with the elusion buffer.
- The AKTP purifier (that runs the FPLC) took real-time UV-vis at 280nm of the run through and elutent from the column. The 280nm peak indicates the presence of protein in the elutent. This UV-vis made it be feasible to identify the test tubes containing the ADA protein.
- The ADA protein was collected in two 5mL test tubes and combined into a 15mL falcon tube. The falcon tubes were stored at 4°C.
Preparing Au/BSA Solutions of AA
- The stock solutions for HAuCl4 and BSA were combined. The moles of each component were calculated in this "new stock" and the BSA needed was calculated so that the desired Au/BSA ratios could be obtained. Please refer to Melissa's entry for tables and specifics including moles, volumes, and edited protocol.