Yu:CoIP

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#Spin down at 3K RPM for 30s and transfer supernatant into new tubes. Save these tubes as '''Supernatant Control'''.
#Spin down at 3K RPM for 30s and transfer supernatant into new tubes. Save these tubes as '''Supernatant Control'''.
#Wash three times with 1 mL completed lysis buffer. Mix very gently by slow inversion each time, and spin down at 3k RPM for 30s.
#Wash three times with 1 mL completed lysis buffer. Mix very gently by slow inversion each time, and spin down at 3k RPM for 30s.
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*For TAP mini-purification, go to [[Yu:CoIP#TEV_Cleavage|TEV Cleavage]]. Otherwise continue.
+
#*For TAP mini-purification, go to [[Yu:CoIP#TEV_Cleavage|TEV Cleavage]]. Otherwise continue.
#Wash with 300 µL 5 mM ammonium acetate, pH 5.0. Save 10 μL from each sample as '''Wash Control''', discard the remaining supernatant.
#Wash with 300 µL 5 mM ammonium acetate, pH 5.0. Save 10 μL from each sample as '''Wash Control''', discard the remaining supernatant.
#Elute with 300 µL 0.5 M acetic acid, pH 3.5. Briefly vortex after adding acetic acid, spin down, and transfer supernatant to a new tube labeled '''Eluate'''.
#Elute with 300 µL 0.5 M acetic acid, pH 3.5. Briefly vortex after adding acetic acid, spin down, and transfer supernatant to a new tube labeled '''Eluate'''.

Revision as of 11:25, 26 September 2009

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Contents

Lysis

FastPrep

  1. Prepare cell pellets.
    1. Grow cell culture to late-log overnight in 5 mL YEPD.
    2. Subclone at 1:100 into 50 mL YEPD and grow until mid-log. This takes approximately 4-6 hours.
    3. Harvest cells and transfer into a FastPrep tube.
  2. Add 100µL completed lysis buffer (PBSMT or NP-40) and approximately 100 µL glass beads. Fastprep twice for 30s at 6.5 each time. Add an additional 500 µL completed lysis buffer and spin down at max speed for 10 minutes.
  3. Transfer supernatant to a fresh eppendorf tube without disturbing pelleted beads.
  4. Perform a Bradford assay on each lysate to determine protein concentration.
  5. Transfer 5 mg protein from each lysate to a fresh eppendorf tube and bring the volume to 1 mL with completed lysis buffer.
  6. Save 10 µL of each diluted lysate as Lysate Control in new tubes.

Preparing Beads

IgG Beads

  1. Thoroughly mix IgG beads in stock bottle by swirling. Open carefully.
  2. Pipette (carefully and slowly) 35 µL of bead slurry into separate eppendorf tubes for each sample. Remix bottle after each aliquot.
  3. Add 1.5 mL TST buffer to each tube, resuspending beads by inversion.
  4. Spin down at 3K rpm for 30s. Carefully pipette off supernatant without disturbing bead pellet.
  5. Wash with 450 µL of 0.5 M acetic acid (pH 3.5). Resuspend beads by inversion and spin down again. Carefully discard supernatant.
  6. Wash with 1.5 mL TST buffer.
  7. Wash with 450 µL of 0.5 M acetic acid (pH 3.5).
  8. Wash twice, using 1.5 mL TST buffer each time.
  9. Add 1.5 ml TST, resuspend beads, and spin down. Test the pH of the supernatant with pH paper. If the pH of the supernatant is below pH 7, discard the supernatant and repeat this step to rewash the beads with TST.
  10. If the pH is 7, discard supernatant and resuspend beads in 55 µL of lysis buffer.

Isolating Protein

TAP Binding

  1. For each sample, add 1mL of 5 mg/mL protein sample to a tube containing washed IgG beads
  2. Incubate slowly rotating at 4°C for 2h to allow ProteinA binding.
  3. Spin down at 3K RPM for 30s and transfer supernatant into new tubes. Save these tubes as Supernatant Control.
  4. Wash three times with 1 mL completed lysis buffer. Mix very gently by slow inversion each time, and spin down at 3k RPM for 30s.
    • For TAP mini-purification, go to TEV Cleavage. Otherwise continue.
  5. Wash with 300 µL 5 mM ammonium acetate, pH 5.0. Save 10 μL from each sample as Wash Control, discard the remaining supernatant.
  6. Elute with 300 µL 0.5 M acetic acid, pH 3.5. Briefly vortex after adding acetic acid, spin down, and transfer supernatant to a new tube labeled Eluate.
  7. Add 20 µL TCA.
  8. Freeze at -20°C overnight.

TEV Cleavage

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