Protein Purification

Overview

Before we could make thin films we had to purify the expressed protein. We tried a number of different methods, mostly based around polyhistidine affinity purification.

We also used an inclusion body prep in order to extract the reflectin, as we already knew that it would localise to inclusion bodies when expressed at high level.

We took aliquots of our purification stages as well as our inclusion body prep stages and ran them on a protein gel with SDS PAGE. This allowed us to both verify that reflectin was being produced, and to detect and improve any lossy steps in the procedure.

Practice

His-Trap Protein Purification - First Attempt

Bacteria expressing his-tagged reflectin were lysed, and the protein was purified using a his-trap column and a denaturing protocol in order to solubilise reflectin. Polyacrylamide gel electrophoresis suggests we have a protein around 30kDa in weight which correlates with the molecular weight of reflectin, but a lack of other evidence means reflectin's presence is not yet certain.

Practice

• After high copy expression plasmids for his-tagged reflectin were successfully assembled and transformed in E. coli, cell cultures were incubated overnight with 1mM arabinose to induce reflectin expression.
• Buffers were prepared, and their pH checked and readjusted if necessary on the day of purification.
• An inclusion body prep was performed with 50ml of overnight culture. Reflectin was purified from the resulting lysate using a his-trap column.
• This procedure was performed using two different cultures of the same bacteria. The culture that produced the highest yield of reflectin was selected as a 'seed' for future cultures that would be used to harvest more protein.

Results

Photospectroscopy readings from the eluted solution indicated that we had obtained approximately 0.4mg of reflectin from the column for the denser culture, and 0.2mg from the other. After dialysis, a vacuum centrifuge was used to precipitate the protein. this precipitate was taken to the Nanophotonics centre in order to make our first reflectin thin films, and SDS-PAGE was run by another member of the department to check whether or not reflectin was contained in the precipitate.

We received gel image (see below) back from Kathryn Lilley who kindly offered to run a protein gel for us. A band at 30-36kDa suggests Reflectin may be present, but we're hoping to use mass spectrometry to confirm this tentative result.

Despite not being certain we had reflectin, we pressed on with our thin films experiment, which produced some very interesting results!

Since this was the first time any of us had tried to perform the his-trap technique, we also learnt some valuable lessons from our experiences in this first experiment. Some helpful tips have been added to the his-trap purification protocol as a result, which really helped us to improve our yield of reflectin using this method.

His-Trap Protein Purification - Second Attempt

Reflectin was harvested from bacteria very similarly to the first attempt, this time attempting both variants of the purification protocol and both nickel and [http://www.abtbeads.com/histagpurification_chelating_beads.html ABT cobalt resin] (kindly donated by Carole Augustus, Thistle Scientific). The culture that provided the higher yield of reflectin last time was harvested in this attempt.

Practice

The methods described in the first attempt at his-trap purification were repeated with two new columns, one containing nickel resin and the other cobalt. The cobalt was also washed through with 6 extra column volumes of sterile water and triple the binding buffer at the start of the protocol, as recommended by the manufacturer. Instead of protein precipitation with dialysis, we attempted acetone precipitation and [[Team:Cambridge/Protocols/Ethanol_Precipitation_of_Proteins | ethanol precipitation] to fully isolate the reflectin product.

Results

A280 readings from the eluted solution indicated that we had obtained approximately 2mg of reflectin from each column, indicating a five-fold increase in our yield. Both acetone and ethanol precipitation worked well, with large pellets visible at the end of the procedures. Based on the thin films made from these samples, the acetone precipitation protocol gives higher purity.

The image below shows the results of an SDS protein gel run on the results, clearly showing bands at 43kDa - the size of reflctin.

The result of the Polyhis affinity column SDS Page gel

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