Difference between revisions of "Glycogen Synthase Assay"

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[[Category:Glycogen]]
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[[Category:Metabolism]]
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[[Category:Cell Culture]]
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==Materials==
 
==Materials==
 
* Glycogen Synthase Buffer ('''GSB''')
 
* Glycogen Synthase Buffer ('''GSB''')
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# Incubate 15 min at 37C with occasional shaking
 
# Incubate 15 min at 37C with occasional shaking
 
# Place on ice for 15 min.
 
# Place on ice for 15 min.
# Spot 90 uL of reaction mixture onto GF/A filters. Wait 3s and immerse in 70% ethanol at 4C
+
# Spot 90 uL of reaction mixture onto GF/A filters.
 +
# Place in a well of a 6 well dish.
 +
# Add ~2mL of ice cold 70% ethanol.
 
# Wash 15 min at 4C
 
# Wash 15 min at 4C
 
# Wash twice 10-20 min at room temperature with fresh 70% ethanol.
 
# Wash twice 10-20 min at room temperature with fresh 70% ethanol.
# Air dry overnight and count in 5 mL scintillation fluid.
+
# Air dry overnight on a paper towel and count in 5 mL scintillation fluid. Also count 5 uL of both the - and + G6P solution to calculate total incorporation

Latest revision as of 13:02, 18 May 2012


Materials

  • Glycogen Synthase Buffer (GSB)
    • 50 mM HEPES
    • 100 mM Sodium fluoride
    • 10 mM EDTA
  • Glycogen (Sigma catalog # ...)
  • Glucose-6-Phosphate (Sigma catalog # G-7879). Dissolve to 200 mM in water
  • UDP-Glucose (Sigma catalog # U-4625). Dissolve to 200 mM in water.
  • 14C-UDP-Glucose (ARC # ARC 0154-50 µCi)

Assay

  1. Serum and glucose deprive cells for 3h in DMEM Low Glucose + 0.5% FBS.
  2. Treat cells as required
  3. Add GSB to cells (1 mL/10cm dish) and scrape
  4. Sonicate 10s then spin 5 min at 3500K in eppendorf centrifuge. Snap freeze supernatants if required, this decreases the absolute but not relative activity.
  5. Prepare reaction mixture (enough for 20 assays):
    1. 1 mL GSB
    2. 16 mg Glycogen (combine these two ahead of time and dissolve at 42C for 10-15 min)
    3. 60 uL of 200 mM UDP Glucose
    4. 1 uCi of 14C-UDP-Glucose
    5. 62.5 uL Water or 200 mM G6P
  6. Assay 50 uL of extract + 50 uL of reaction mixture. Do in triplicate -/+ G6P.
  7. Incubate 15 min at 37C with occasional shaking
  8. Place on ice for 15 min.
  9. Spot 90 uL of reaction mixture onto GF/A filters.
  10. Place in a well of a 6 well dish.
  11. Add ~2mL of ice cold 70% ethanol.
  12. Wash 15 min at 4C
  13. Wash twice 10-20 min at room temperature with fresh 70% ethanol.
  14. Air dry overnight on a paper towel and count in 5 mL scintillation fluid. Also count 5 uL of both the - and + G6P solution to calculate total incorporation