Difference between revisions of "Affinity Purification of Proteins - FPLC"
From Bridges Lab Protocols
Davebridges (Talk | contribs) (added details from new run) |
Davebridges (Talk | contribs) (reworded some bits of the protocol) |
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==HPLC Setup== | ==HPLC Setup== | ||
| + | Normally steps 1-7 are already done. If you have any questions ask Colin or Dave. | ||
#Check that the HPLC is set up for protein work and not radioactive work (see [[HPLC - Plumbing Setup]]). | #Check that the HPLC is set up for protein work and not radioactive work (see [[HPLC - Plumbing Setup]]). | ||
#Turn on computer, pumps and lamp if not already on by pressing the buttons on the front. | #Turn on computer, pumps and lamp if not already on by pressing the buttons on the front. | ||
#Using TC Navigator, attach the HPLC (if not attached). | #Using TC Navigator, attach the HPLC (if not attached). | ||
#Disconnect the column from the top (if already connected). | #Disconnect the column from the top (if already connected). | ||
| − | #Load the desired method, or write a new one (see [[HPLC - Designing a Method for a Sample or Series]]) | + | #Load the desired method, or write a new one (see [[HPLC - Designing a Method for a Sample or Series]]). Save both the raw and results file to a folder with your name on it and name it as YYYY-MM-DD-SampleName. |
#Go to setup and choose where to save your data. | #Go to setup and choose where to save your data. | ||
#Click Hands On and click Start Pump, and on the Detector Tab Click Lamp On (if they are not on already). | #Click Hands On and click Start Pump, and on the Detector Tab Click Lamp On (if they are not on already). | ||
| Line 16: | Line 17: | ||
##Move the protein lead into the protein sample and re-prime with protein (until protein is visible in the syringe). This is done so that the protein sample is only mixed with the equillibration buffer, and this mixture can be added back to the protein sample. | ##Move the protein lead into the protein sample and re-prime with protein (until protein is visible in the syringe). This is done so that the protein sample is only mixed with the equillibration buffer, and this mixture can be added back to the protein sample. | ||
##Prime the Elution buffer. | ##Prime the Elution buffer. | ||
| − | ## | + | ##Reprime with the Wash/Equillibration Buffers |
#Let the equillibration/wash buffer run for a few minutes. | #Let the equillibration/wash buffer run for a few minutes. | ||
#Connect the inlet tube to the top of the affinity column (it should still be running wash/equillibration buffer) using the appropriate fittings. | #Connect the inlet tube to the top of the affinity column (it should still be running wash/equillibration buffer) using the appropriate fittings. | ||
| Line 23: | Line 24: | ||
#Set up the Fraction Collector as desired. | #Set up the Fraction Collector as desired. | ||
#Check the absorbance (normally 280nm) on the setup panel to ensure that it is ~0. If it is not, let it equillibrate a few more minutes and check it again. If the absorbance is >0.3 then the buffer is absorbing too much light at 280nm. If that is the case, use a method with no UV and turn off the UV lamp from the setup panel. | #Check the absorbance (normally 280nm) on the setup panel to ensure that it is ~0. If it is not, let it equillibrate a few more minutes and check it again. If the absorbance is >0.3 then the buffer is absorbing too much light at 280nm. If that is the case, use a method with no UV and turn off the UV lamp from the setup panel. | ||
| − | #Once everything is ok (and the status panel is marked ready), start the run by turning the injector port to load. If you are loading sample via the pump, either port will work (and can be turned immediately back to the load position). If you are loading via the sample loops, wait until 5 times the loop volume has passed through before turning back. | + | #Once everything is ok (and the status panel is marked ready), start the run by turning the injector port to load. If you are loading sample via the pump, either port will work (and can be turned immediately back to the load position). If you are loading via the sample loops, wait until ~5 times the loop volume has passed through before turning back. |
#Check your progress by clicking the real time monitor button. | #Check your progress by clicking the real time monitor button. | ||
#The program should use your entire protein sample plus ~ 10mL. Midway through your run, as the protein starts to run out, add extra equillibration buffer to rinse the tube. | #The program should use your entire protein sample plus ~ 10mL. Midway through your run, as the protein starts to run out, add extra equillibration buffer to rinse the tube. | ||
Latest revision as of 19:47, 9 February 2011
Preparation of Lysates and Buffers
- Lysates can be prepared by any means, but must be filtered through a 0.22 micron filter (ie a steriflip) prior to applying to the column. If filtering is slow, do a second high speed spin on the supernatant.
- Filter all buffers through a 0.22 micron filter. You need an extra ~50 mL of buffer for priming the pumps
HPLC Setup
Normally steps 1-7 are already done. If you have any questions ask Colin or Dave.
- Check that the HPLC is set up for protein work and not radioactive work (see HPLC - Plumbing Setup).
- Turn on computer, pumps and lamp if not already on by pressing the buttons on the front.
- Using TC Navigator, attach the HPLC (if not attached).
- Disconnect the column from the top (if already connected).
- Load the desired method, or write a new one (see HPLC - Designing a Method for a Sample or Series). Save both the raw and results file to a folder with your name on it and name it as YYYY-MM-DD-SampleName.
- Go to setup and choose where to save your data.
- Click Hands On and click Start Pump, and on the Detector Tab Click Lamp On (if they are not on already).
- Rinse the buffer leads with water and place into the appropriate buffers (see the Hands On page for which lead corresponds to which buffer).
- Prime the pumps in the following order by putting the buffer lead into the correct bottle, switching the pump to 100% of that buffer, unscrewing the black wheel in the pump (remove the panel) and sucking up ~25 mL of liquid with a 60 mL syringe:
- Place the protein lead into the equillibration buffer and prime.
- Move the protein lead into the protein sample and re-prime with protein (until protein is visible in the syringe). This is done so that the protein sample is only mixed with the equillibration buffer, and this mixture can be added back to the protein sample.
- Prime the Elution buffer.
- Reprime with the Wash/Equillibration Buffers
- Let the equillibration/wash buffer run for a few minutes.
- Connect the inlet tube to the top of the affinity column (it should still be running wash/equillibration buffer) using the appropriate fittings.
- Connect the bottom of the column to the tube leading into the UV monitor.
- Check all connections for leaks.
- Set up the Fraction Collector as desired.
- Check the absorbance (normally 280nm) on the setup panel to ensure that it is ~0. If it is not, let it equillibrate a few more minutes and check it again. If the absorbance is >0.3 then the buffer is absorbing too much light at 280nm. If that is the case, use a method with no UV and turn off the UV lamp from the setup panel.
- Once everything is ok (and the status panel is marked ready), start the run by turning the injector port to load. If you are loading sample via the pump, either port will work (and can be turned immediately back to the load position). If you are loading via the sample loops, wait until ~5 times the loop volume has passed through before turning back.
- Check your progress by clicking the real time monitor button.
- The program should use your entire protein sample plus ~ 10mL. Midway through your run, as the protein starts to run out, add extra equillibration buffer to rinse the tube.
