User:Ryanliang

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'''8/13'''
 
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Tranfections
 
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1. Car1-FRB
 
-
 
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2. hM4
 
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3. SSF-YFP-hM4D-βPix
 
-
 
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4. hM4D Act A Long
 
-
 
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5. hM4D Act A Short
 
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6. hM4D LPD Short
 
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Transfection Efficiency
 
-
 
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Car1-FRB: 42.4%
 
-
 
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hM4:  42.4%
 
-
 
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SSF-YFP-hM4D-βPix: 40.4%
 
-
 
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hM4D Act A Long: 46.4%
 
-
 
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hM4D Act A Short: 36.5%
 
-
 
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hM4D LPD Short: 44.3%
 
-
 
-
 
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Chemoattractant Dilutions
 
-
 
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CNO [0nM, 10nM, 100nM, 1uM]
 
-
 
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cAMP [0nM, 10nM, 100nM, 1uM]
 
-
 
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fMLP [100nM]
 
-
 
-
 
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Result: hM4D worked only
 
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-
 
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'''8/12'''
 
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Transfections
 
-
 
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1. GPR132
 
-
 
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2. LPA1
 
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3. OPRL1
 
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4. Control
 
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-
 
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Transfection Efficiency:
 
-
 
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GPR132: 41%
 
-
 
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LPA1: 43.2%
 
-
 
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OPRL1: 50%
 
-
 
-
 
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Chemoattractant Dilutions
 
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LPC: [0nM, 10nM, 100nM, 1uM]
 
-
 
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LPA: [0nM, 100nM, 500nM, 1uM]
 
-
 
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Orphanin FQ: [0nM, 1nM, 10nM, 100nM]
 
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fMLP [100nM]
 
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-
 
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RESULTS: OPRL1 worked only
 
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'''8/10'''
 
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Transfections
 
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1. DOR
 
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2. DOR ACTININ
 
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3. DOR ERM
 
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4. DOR EZRIN
 
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5. DOR KIFC
 
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6. DOR VHEAD
 
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7. hM2D
 
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8. hM3D
 
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9. hM3.2D
 
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10. Control
 
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Transfection Efficiency:
 
-
 
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DOR: 40.9%
 
-
 
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DOR ACTININ: 39.5%
 
-
 
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DOR ERM: 47.5%
 
-
 
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DOR EZRIN: 48.1%
 
-
 
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DOR KIFC: 39.2%
 
-
 
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DOR VHEAD: 32.1%
 
-
 
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hM2D: 35.2%
 
-
 
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hM3D: 51%
 
-
 
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hM3.2D: 54.7%
 
-
 
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Chemoattractant Dilutions
 
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DADLE [0nM, 1nM, 10nM, 100nM]
 
-
 
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CNO [0nM, 10nM, 100nM, 1uM]
 
-
 
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fMLP [100nM]
 
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-
 
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Results: DOR, DOR ACTININ, DOR EZRIN, DOR KIFC, DOR VHEAD, and hM3.2D worked
 
-
 
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'''8/6'''
 
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Transfections
 
-
 
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1. ADRA1A
 
-
 
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2. EDG1
 
-
 
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3. GRM2
 
-
 
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4. GRM4
 
-
 
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5. MTNR1A
 
-
 
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6. OPRL1
 
-
 
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7. VIB
 
-
 
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8. Control
 
-
 
-
 
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Chemoattractant Dilutions
 
-
 
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Epinephrine: [0nM, 10nM, 100nM, 1000nM]
 
-
 
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S1P: [0nM, 10nM, 100nM, 1uM]
 
-
 
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Glutamate: [0nM, 10nM, 100nM, 1uM]
 
-
 
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CNO [0nM, 10nM, 100nM, 1uM]
 
-
 
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Melatonin: [0nM, 1nM, 10nM, 1uM]
 
-
 
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Orphanin FQ: [0nM, 1nM, 10nM, 100nM]
 
-
 
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Vasopressin [0nM, 10nM, 100nM, 1uM]
 
-
 
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fMLP: [100nM]
 
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-
 
-
 
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'''8/5'''
 
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Transfections
 
-
 
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1. CCR7
 
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2. DOR
 
-
 
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3. DOR ERM
 
-
 
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4. DOR EZRIN
 
-
 
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5. DOR KIFC
 
-
 
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6. DOR VHEAD
 
-
 
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7. hM3
 
-
 
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8. Hm3.2
 
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9. Control
 
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Transfection Efficiency:
 
-
 
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CCR7: 45.2%
 
-
 
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DOR: 62.8%
 
-
 
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DOR ERM: 45.7%
 
-
 
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DOR EZRIN: 40%
 
-
 
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DOR KIFC: 35.2%
 
-
 
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DOR VHEAD: 42.4%
 
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hM3: 47.4%
 
-
 
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hM3.2: 30.9%
 
-
 
-
 
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Chemoattractant Dilutions:
 
-
 
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MIP-3Beta (0ug/ml, 0.01ug/ml, 0.1ug/ml, 1ug/ml)
 
-
 
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DADLE [0nM, 10nM, 100nM, 1uM]
 
-
 
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CNO [0nM, 10nM, 100nM, 1uM]
 
-
 
-
 
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RESULTS: Wildtype cells did not stain so our data is unreliable so we have to redo all these GPCRs and RASSLs. Of the results, it shows that CCR7, DOR, DOR EZRIN, DOR KIFC, DOR VHEAD, and hM3.2 migrated. DOR KIFC is a maybe. When we redo it, we will change the concentrations to 10x lower.
 
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'''8.4'''
 
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Transfections
 
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1.ADRA1A
 
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2.EDG1
 
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3.GPR132
 
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4.GRM2
 
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5.GRM4
 
-
 
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6.hM3
 
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7.LPA1
 
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8.MTNR1A
 
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9.OPRL1
 
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10.V1B
 
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11. Control
 
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-
 
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Chemoattractant Dilutions
 
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Epinephrine: [0nM, 10nM, 100nM, 1000nM]
 
-
 
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S1P: [0nM, 10nM, 100nM, 1uM]
 
-
 
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LPC: [0nM, 10nM, 100nM, 1uM]
 
-
 
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Glutamate: [0nM, 10nM, 100nM, 1uM]
 
-
 
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CNO [0nM, 10nM, 100nM, 1uM]
 
-
 
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LPA: [0nM, 100nM, 500nM, 1uM]
 
-
 
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Melatonin: [0nM, 1nM, 10nM, 1uM]
 
-
 
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Orphanin FQ: [0nM, 1nM, 10nM, 100nM]
 
-
 
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Vasopressin [0nM, 10nM, 100nM, 1uM]
 
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fMLP: [100nM]
 
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RESULTS: None, machine broke, redo 8/6
 
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'''8/3'''
 
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Transfections
 
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1. AGTR1
 
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2. AGTR2
 
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3. B2AR
 
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4. B2AR EZRIN
 
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5. hM3.2
 
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6. hM4
 
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7. HTR1A
 
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8. HTR2B
 
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9. HTR7A
 
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10. Rs1
 
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11. Rs1.3
 
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12. Control
 
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Chemoattractant Dilutions:
 
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Isoprenaline [0nM, 1nM, 10nM, 100nM]
 
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CNO: [0nM, 10nM, 100nM, 1uM]
 
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Zacopride: [0nM, 10nM, 100nM, 1uM]
 
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Angiontensin II (0nM, 1nM, 10nM, 100nM)
 
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Seratonin (0nM, 10nM, 100nM, 1000nM)
 
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Glutamate [0nM, 10nM, 100nM, 1uM]
 
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fMLP: [100nM]
 
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-
 
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'''7/31'''
 
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Goal: Combine WT cells and GPCR cells in the same well/insert only if we can give WT RFP.
 
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1. Transfection with DsRed2 and mCherry
 
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2. Dye cells with Red Vybrant @ 0,1,2,5,15,20 minutes
 
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DsRed2 and mCherry takes too long to show RFP (5+ hours)
 
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Cells are dyed at the optimum amount by 15minutes.
 
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'''7/29'''
 
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Transwell
 
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Test new and old stocks of CNO in Millipore and BD
 
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Chemoattractant Dilutions:
 
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fMLP [100nM]
 
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CNO [10nM, 100nM] Old & New
 
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'''7/28'''
 
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Transfections
 
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hM4 Transients in Millipore, BD, and Corning
 
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Chemoattractant Dilutions:
 
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CNO [0nM, 10nM, 100nM, 1uM]
 
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fMLP [10mM]
 
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RESULTS: BD is best
 
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'''7/27'''
 
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Site DIrected Mutagenesis of DOCK insert in pTOPO
 
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Picked colonies for AB-SSF pDONR221-PL-Flag, PCR2.1 TOPO-ITSN, PCR2.1 TOPO-TUBA, pDONR221-LPD775-1250aa, AB-YFP pDONR221-PL-FLAG-YFP, and TOPO-LPD full
 
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'''7/21'''
 
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Transfections
 
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1. ADRA1A
 
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2. B2AR
 
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3. B2AR EZRIN
 
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4. HTR1A
 
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5. HTR2B
 
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6. GPR132
 
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7. LPA1
 
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8. Control
 
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-
 
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Chemoattractant Dilutions:
 
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Epinephrine (0nM, 10nM, 100nM, 1000nM)
 
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Isoprenaline(0nM, 100pM, 1nM, 10nM)
 
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LPA (0nM, 100nM, 500nM, 1uM)
 
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LPC (0nM, 10nM, 100nM, 1uM)
 
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Serotonin (0nM, 10nM, 100nM, 1000nM)
 
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-
 
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'''7/20'''
 
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Transfections
 
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1. AGTR1
 
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2. AGTR2
 
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3. CCR7
 
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4. GRM2
 
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5. GRM4
 
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6. MTNR1A
 
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7. OPRL1
 
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8. VIB
 
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9. Control
 
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Dilution Calculations
 
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Angiontensin II (0nM, 1nM, 10nM, 100nM)
 
-
 
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MIP-3Beta (0ug/ml, 0.01ug/ml, 0.1ug/ml, 1ug/ml)
 
-
 
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Vasopressin (0nM, 10nM, 100nM, 1uM)
 
-
 
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Orphanin FQ [0nM, 1nM, 10nM, 100nM]
 
-
 
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Glutamate [0nM, 10nM, 100nM, 1uM]
 
-
 
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Melatonin [0nM, 1nM, 10nM, 1uM]
 
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-
 
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'''7/15'''
 
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Transfections
 
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1. AGTR1
 
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2. AGTR2
 
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3. GRM2
 
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4. GRM4
 
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5. MTNR1A
 
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6. OPRL1
 
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7. Control
 
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'''7/14'''
 
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Redo Unsuccessful Control Digestions
 
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SAMPLE 5' ENZYME 3' ENZYME BUFFER POSITIVE
 
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GRM4 BamH1               Xba1 2 YES
 
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HTR7A EcoR1               Xba1 2 NO
 
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GPR132 EcoR1               Xho1 2 YES
 
-
EDG1 BamH1               Xho1 2 NO
 
-
RO2 Xma1               none 4 NO
 
-
Rs1.3 Not1               none 3 NO
 
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hM4D Nhe1               none 2 YES
 
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hM2D Xma1               none 4 NO
 
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Rs1 HindIII              none 2 YES
 
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Dump unsuccessful control samples, either we retransform or repick colonies.
 
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'''7/13'''
 
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Miniprep/Aar1 digestion of hM4D, Rs1.3, YFP, SSF
 
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Digestion#2 (CONTROL DIGEST)
 
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PLASMID 5' ENZYME 3' ENZYME INSERT SIZE BUFFER POSITIVE
 
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MNTR1A            EcoR1     Xho1       1052 2 YES
 
-
GRM4             BamH1     Xba1       2739 2 NO
 
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AGTR2             EcoR1     Xho1       1092 2 YES
 
-
AGTR1             EcoR1     Xho1       1080 2 YES
 
-
GRM2             BamH1     Xho1       2619 3 YES
 
-
HTR7A             EcoR1     Xba1       1338 2 NO
 
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HTR2B             BamH1          Xho1       1445 3 YES
 
-
V1B             BamH1      Xho1       1275 3 YES
 
-
CCR7             EcoR1     Xho1       1137 2 YES
 
-
GPR132             EcoR1     Xho1       1143 2 NO
 
-
EDG1             BamH1     Xho1       1149 3 NO
 
-
EDG2             BamH1     Xho1       1095 3 YES
 
-
OPRL1             EcoR1     Xho1       1113 2 YES
 
-
ADRA1A             EcoR1     Xho1       1401 2 YES
 
-
HTR1A             BamH1     Xho1       1270 3 YES
 
-
Ro2             Xma1     none              1646 4 NO
 
-
hM3.2             BamH1     none       944 3 YES
 
-
Rs1.3             Not1     none       1448 3 NO
 
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hM2D             Xma1     none       1353 4 NO
 
-
hM4D             Nhe1     none       1260 2 NO
 
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'''7/9'''
 
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Did minipreps for multiple pMAX-GFP colonies, combined all the plasmids into one microcentrifuge and the yield was 249.4ng/ul.
 
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Made a digestion, Cathy ran a gel
 
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Cathy, and I worked on analyzing FACS results from Tuesday and Wednesday's transwells/transfections. Analyzed data on the Flowjo program; organized the data on excel, then put the results on a bar graph.
 
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'''7/8'''
 
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Transwell
 
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8 variations of the RASSL hM4.
 
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The 8 were L1, L2, L3, M1, M2, H1, H2, and H3
 
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Chemoattractant Dilutions
 
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CNO (0nM, 10nM, 100nM, 1uM)
 
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'''7/7'''
 
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Transfection (Contransfection)
 
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Add two constructs/vectors into our HL-60 cell line (RASSL + pMAXGFP)
 
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Use 5 days HL-60 differentiated with DMSO
 
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Transfected hM2, hM3, hM4, Rs1.3, all including pMAXGFP into HL-60 cells
 
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Incubate in 37C for 4 hours.
 
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Used for transwell assay.
 
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CNO Dilution is 10nM
 
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fMLP Dilution is 10nM
 
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'''7/6'''
 
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We used Amaxa transfection to get pMAX GFP DNA into 4 days HL-60 cells
 
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Protocol provided from: http://cellpropulsionlab.pbworks.com (copied over from limwiki.ucsf.edu)
 
-
 
-
100ml monocyte media for HL-60 cells
 
-
 
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78ml Gibco IMDM
 
-
 
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20ml 20% FBS
 
-
 
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1ml Glutamate
 
-
 
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1ml Antibiotic/Antimycotics
 
-
 
-
 
-
 
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2.75ml Nucleofector solution
 
-
 
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2.25ml Cell Line Nucleofector Solution V
 
-
 
-
.50ml Supplement
 
-
 
-
 
-
Positive transfection showed cells with green fluorescence, there was about 40% fluorescence meaning 40% success rate.
 
-
We have to note that using the right centrifuge makes a difference in transfection results. Using the incorrect centrifuge resulted in lower cell count and a 30% fluorescence while the correct centrifuge resulted in a much higher cell count as well as a fluorescence of 70%.
 
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-
GPCR Miniprep
 
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alpha-pix, intersectin, P-Rex 5, DOR-ERM, DOR EZRIN, B2AR, LPD 775-1250, BPRX GFP-VASP, GFP-VASP BPRX
 
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Transformations
 
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DOR-KIFC, DOR-ACTININ, B2AR ACTININ, LPD 775-1250, ActA 30-612, ActA 225-392, Vav, and Beta-Pix
 
-
 
-
50ul  Competent cells (DH5-alpha)
 
-
 
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50ul  1x PCM (40ul water/10ul 5x PCM)
 
-
 
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1ul    Plasmid
 
-
 
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101ul    TOTAL
 
-
 
-
 
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Plated on CarB+Amp, incubating at 37C
 
-
 
-
'''7/2'''
 
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Cathy, Caitlin and I learned how to analyze our cells with the FACS machine. Sometimes the FACS machine is not accurate, so we add beads to increase accuracy.
 
-
The machine takes about 40 seconds per sample, we had 56 samples.
 
-
 
-
Beads stock is 1,000,000beads/ml, we used 25ul which is 25,000 beads.
 
-
If we have 100 cells and 20,000 beads shown on the FACS, then we can assume that only 80% (20,000 of 25,000) of the cells and beads are shown, So 100% of the cells would be 125 cells.
 
-
I learned how to analyze these numbers on a computer program Flowjo, excel, as well as on a graph.
 
-
 
-
'''7/1'''
 
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Practice a second protocol runthrough of Transwell assay
 
-
 
-
'''6/29'''
 
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First protocol runthrough of Transwell assay
 
-
 
-
'''6/25'''
 
-
Ran gels and checked dictyostellium confluency
 
-
 
-
'''6/23-6/18'''
 
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Plate dicty, run gels, do minipreps, and purify plasmids
 

Latest revision as of 01:16, 13 October 2009