Team:Freiburg Bioware/NoteBook/Labjournal/October

Analysis of viral harvest via spectrometer

Investigator: Adrian, Patrick

The motivation: We want to figure out if it is possible to purify our viral stocks via centrifugation with 10.000 g and/or 20.000 g. In theory/ according to the literature the viral particles should be in the cells and attached to the HSPGs at the cellular surfaces.
The plan: Two different viral stocks were prepared:

Stock 1 with VP2-mVenus-fusion-Capsid loaded with TKGMK (4 wells from a 6 well plate)

• R/C 1: 50% pCerulean_VP1up_NLS_mVenus_Vp2/3 P501
• R/C 2: 50% Rep/Cap2: P449 pAAV_RC_4fachmut_VP1-ko:
• GOI: TKGMK: P82.b
• pHelper

Stock 2 "standard" virus (4 wells from a 6 well plate)

• R/C 1 P486
• GOI: TKGMK: P82.b
• pHelper

These two stocks got harvested according to standard protocol (scratching cells, transfer them in to 15 ml falcons, resuling 12ml solution total). After centrifugation (10 min 200g), the supernatant got transferred into two new 15 ml falcons and the pellets were resuspended with 10 ml DMEM Medium. The Stocks got freezed thawed two times so finally there were:

1. DMEM as negative control
2. resuspended Pellet with mVenus-fusioned viral capsids
3. resuspended Pellet with "standard virus"
4. supernatant with mVenus-fusioned viral capsids
5. supernatant with "standard virus"

The fluorescence of each stock was measured via spectrometer. After that, stocks 2 and 4 were centrifugated 10min with 10.000 g followed by an other fluorescence measuring. Finally the stocks got spin down with 20.000 g for 10 min
The results:

The conclusions: The highest amount of fluorescence was measured in the supernatant, the individual centrifugation steps had no decrease in fluorescence as consequence!

Keep in mind, without further investigation it is not valid to say that we can purify our stocks via 10-20.000 g centrifugation steps, because we dont know if the viral capsids are still intact! The FACS analysis are not sufficient enough to make a decision, because our last samples had YFP as GOI (=> so efficient cell sorting was not possible). We need to do qPCRs to make a valid evidence.

200µl-Transduction for testing the pTERT-promoter

Investigator: Adrian, Patrick
We transduced A431, HT1080 and AAV293 cells with 4 different viral stocks:

1. control vector from 15.9, 750.000 cells, 3.3 µg approach
2. P25 R/C= 326 pTERT_mVenus
3. P26 pAAV_RC_RepCapIns_SDMKpnI clone 1 P431 pTERT_mVenus
4. His-linker-fusion

CRUCIAL: There was not enough viral stock: so the whole Transduction was performed with 200µl instead of 1000µl

There are 45 samples to FACS on monday 4.10. Tripple values for each stock of each cell lines.

Transfection

Investigators: Adrian, Patrick
Transfection followed standard protocol (3.3 µg of each plasmid, 1 ml 0.3M CaCl₂ and 1 ml of 2xHBS buffer PH 11.12) but with 20 min incubation time (Ca-DNA-2xHBS)
following stocks:

• mVenus standard stock 10 x cm R/C: P468² plates
• TKGMK stock 10 x cm² plates R/C: P468
• viral particles with GOI (mVenus) missing HGH one 6well plate
• viral particles with GOI (mVenus) missing beta globin one 6well plate
• viral particles with R/C missing HSPG binding motif (P687) one 6well plate
• viral particles with new standard R/C (P668) one 6well plate

138. labday 03.10.2010

Proceeding with the approach of subcloning the ViralBricks HSPG-ko BAP and His into VP2/3 with different strategies

Investigator: Bea

Comment: Ligation was carried out over night and transformation will be performed today.

Since the digested vector was not sufficient for all four ligation I decided to perform the ligation only with the hybridized oligos 587-ko His and the digested Viralbricks 587-HSPG-ko His and BAP. If the digested BAP insert reverals no positive results, the hybrizied oligos for BAP can be used for another approach. The transformation was carried out in

• BL-21 cells
• and plated on agar plastes containing chloramphenicol

Midi-Prep of pSB1C3_lITR_CMV_betaglobin_mVenus_hGH_rITR clone1

Investigator: Chris W.

Midi-Preps of pSB1C3_lITR_CMV_betaglobin_mVenus_hGH_rITR clone1 =P713 =B200

The Midi-Prep were performed according to the standard protocol yielding the following concentrations:

plasmid-no.	P713
concentration (ng/µl)	1248,3

139. labday 04.10.2010

Three fragment ligation: pSB1C3_001_CMV_VP1up_NLS_Targeting_HSPG-KO_VP2/3

Investigator: Achim

Four ligations in total:

• Cloning CMV & VP1up_NLS_mVenus_HSPG-KO_VP2/3 into pSB1C3_001
• Cloning CMV & VP1up_NLS_His_HSPG-KO_VP2/3 into pSB1C3_001
• Cloning CMV & VP1up_NLS_affibody_HSPG-KO_VP2/3 into pSB1C3_001
• Cloning CMV into pSB1C3_001

Used plasmids:

• pSB1C3_CMV (P145)
  • c=225.5 ng/µl -> 8 µl
  • Cut with EcoRI & SpeI
• pCerulean_VP1up_NLS_mVenus_HSPG-KO_VP2/3 (P711)
  • c=3030 ng/µl -> 0.7 µl
  • Cut with XbaI & PstI
• pCerulean_VP1up_NLS_His_HSPG-KO_VP2/3 (P710)
  • c=2965 ng/µl -> 0.7 µl
  • Cut with XbaI & PstI
• pCerulean_VP1up_NLS_affibody_HSPG-KO_VP2/3 (P709)
  • c=2913 ng/µl -> 0.7 µl
  • Cut with XbaI & PstI
• pSB1C3_001_BLA (P320)
  • c=408.5 ng/µl -> 5 µl
  • Cut with EcoRI & PstI for three fragment ligations
  • Cut with EcoRI & SpeI for ligation with CMV

´Seeding AAV293 for Transfection

Investigator: Patrick

9 6-well plates were prepared for the transfection tomorrow. 480000 cells were seeded into each well.

FACS Analysis of pTERT_mVenus-loaded-viral particles and pCerulean_VP1up_His_VP2/3

Investigators: Kerstin, Anissa

45 samples of the three cell lines: AAV293, A431 and HT1080 got transduced (see 2.10) with following viral stocks:

1.

• pHelper
• R/C : 326
• pTERT-mVenus

2.

• pHelper
• R/C : P431
• pTERT-mVenus

3.

• pHelper
• R/C P158a
• CMV_mVenus

4.

• pHelper
• R/C: pCerulean_VP1up_His_VP2/3
• pAAV_RC_4fachmut_VP1-ko
• CMV_mVenus

Assembly of pSB1C3_CMV_DARPin_VP2/3_insCap and pSB1C3_CMV_DARPin_VP2/3_HSPG-KO

Investigators: Hanna

Comment: We also want to test the DARPin_E01 for the N-terminal fusion approaches. Today a 3 fragment ligation will be performed in order to complete the VP2 fusion constructs with the DARPin.
Because 2 test digestions showed that the fusion of the DARPin to VP1up_NLS didn't work as ecpected (insert is too large) this has to be repeated before also the VP1 insertion with the DARPin can be completed.

Digestion

components	volume of pSB1C3_CMV /µl	volume of pG14_ML_VP2/3_insCap /µl	volume of pG14_ML_VP2/3_HSPG-KO /µl	volume of pSB1C3_001_DARPin /µl
DNA	9	6.8	10	5
BSA (10x)	2	3	3	2
Buffer 4 (10x)	2	3	3	2
SpeI	1	-	-	-
PstI	1	1	1	-
NgoMIV	-	1	1	-
XmnI	-	1	1	-
XbaI	-	-	-	4
H2O	5	14.2	11	9
Total volume	20	30	30	20

• Incubation: 2.5 h

Agarose-Gel:

0.5 g Agarose, 50 mL TAE (1 %), 3 µL GELRED, at 115 Volt, running time: 45 minutes

Sample	Sample/µl]	Loading dye (6x)/µl	Expected size 1
CMV	20 µl	4 µl	~ 2700 bp
MiddleLinker_VP2/3_insCap	30 µl	4 µl	~ 2000 bp
MiddleLinker_VP2/3_HSPG-KO	30 µl	4 µl	~ 2000 bp
DARPin	20 µl	4 µl	~ 475 bp

Gelex

• CMV: 48.99 ng/µL
• MiddleLinker_VP2/3_insCap: 12.95 ng/µL
• MiddleLinker_VP2/3_HSPG-KO ng/µL
• DARPin: 9.59 ng/µL

Ligation

Construct	CMV (µl)	MiddleLinker_VP2/3_insCap (µl)	DARPin (µl)
pSB1C3_CMV_DARPin_MiddleLinker_VP2/3_insCap	1	3.5	3.5

Construct	CMV (µl)	MiddleLinker_VP2/3_HSPG-KO (µl)	DARPin (µl)
pSB1C3_CMV_DARPin_MiddleLinker_VP2/3_HSPG-KO	1	3.5	3.5

Trafo

Was performed following the standard protocol.
Cells: XL1b

Miniprep of serveral constructs

Investigator: Stefan

Glycerol stocks were prepared:
B573 pSB1C3_lITR_CMV_betaglobin_mCherry clone1
B574 pSB1C3_lITR_CMV_betaglobin_mCherry clone2
B575 pSB1C3_lITR_CMV_betaglobin_CD clone1
B576 pSB1C3_lITR_CMV_betaglobin_CD clone2
B577 pSB1C3_lITR_phTERT_betaglobin_mCherry clone1
B578 pSB1C3_lITR_phTERT_betaglobin_mCherry clone2
B579 pSB1C3_lITR_phTERT_betaglobin_CFP_hgH_rITR clone 1
B580 pSB1C3_lITR_phTERT_betaglobin_CFP_hgH_rITR clone 2
B581 pSB1C3_lITR_phTERT_betaglobin_CFP_hgH_rITR clone 1
B582 pSB1C3_lITR_phTERT_betaglobin_CFP_hgH_rITR clone 2
B583 pSB1C3_lITR_phTERT_betaglobin_CD clone 1
B584 pSB1C3_lITR_phTERT_betaglobin_CD clone 2
B585 pSB1C3_lITR_phTERT_betaglobin_CD clone 3
B586 pSB1C3_001_VP2/3_capins_587_KO_His_clone1
B587 pSB1C3_001_VP2/3_capins_587_KO_His_clone2
B588 pSB1C3_001_VP2/3_capins_587_KO_His_clone3
B589 pSB1C3_001_VP2/3_capins_587_KO_His_oligo_clone1
B590 pSB1C3_001_VP2/3_capins_587_KO_His_oligo_clone2
B591 pSB1C3_001_VP2/3_capins_587_KO_His_oligo_clone3
B592 pSB1C3_001_VP2/3_capins_587_KO_Bap_clone1
B593 pSB1C3_001_VP2/3_capins_587_KO_Bap_clone2
B594 pSB1C3_001_VP2/3_capins_587_KO_Bap_clone3

Mini-Prep was performed according to the standard protocol

P714 pSB1C3_lITR_CMV_betaglobin_mCherry clone1 c = 89,3 ng/µl
P715 pSB1C3_lITR_CMV_betaglobin_mCherry clone2 c = 312,4 ng/µl
P716 pSB1C3_lITR_CMV_betaglobin_CD clone1 c = 254,4 ng/µl
P717 pSB1C3_lITR_CMV_betaglobin_CD clone2 c = 314,8 ng/µl
P718 pSB1C3_lITR_phTERT_betaglobin_mCherry clone1 c = 409,8 ng/µl
P719 pSB1C3_lITR_phTERT_betaglobin_mCherry clone2 c = 322,1 ng/µl
P720 pSB1C3_lITR_phTERT_betaglobin_CFP_hgH_rITR clone 1 c = 265,1 ng/µl
P721 pSB1C3_lITR_phTERT_betaglobin_CFP_hgH_rITR clone 2 c = 238,8 ng/µl
P722 pSB1C3_lITR_phTERT_betaglobin_mGMK_TK30_hgH_rITR clone 1 c = 145,9 ng/µl
P723 pSB1C3_lITR_phTERT_betaglobin_mGMK_TK30_hgH_rITR clone 2 c = 100,5 ng/µl
P724 pSB1C3_lITR_phTERT_betaglobin_CD clone 1 c = 176,9 ng/µl
P725 pSB1C3_lITR_phTERT_betaglobin_CD clone 2 c = 165,0 ng/µl
P726 pSB1C3_lITR_phTERT_betaglobin_CD clone 3 c = 149,0 ng/µl
P727 pSB1C3_CMV c = 225,5 ng/µl
P728 pSB1C3_hGH_rITR c = 129,6 ng/µl
P729 pSB1C3_leftITR_CMV_beta-globin c = 243,4 ng/µl
P730 pSB1C3_leftITR_hTERT_beta-globin c = 81,8 ng/µl
P731 pSB1C3_001_VP2/3_insCap c = 466,1 ng/µl
P732 pSB1C3_001_VP2/3_capins_587_KO_His_clone1 c = 107,6 ng/µl
P733 pSB1C3_001_VP2/3_capins_587_KO_His_clone2 c = 110,3 ng/µl
P734 pSB1C3_001_VP2/3_capins_587_KO_His_clone3 c = 121,7 ng/µl
P735 pSB1C3_001_VP2/3_capins_587_KO_His_oligo_clone1 c = 101,0 ng/µl P736 pSB1C3_001_VP2/3_capins_587_KO_His_oligo_clone2 c = 101,6 ng/µl
P737 pSB1C3_001_VP2/3_capins_587_KO_His_oligo_clone3 c = 87,0 ng/µl
P738 pSB1C3_001_VP2/3_capins_587_KO_Bap_clone1 c = 106,5 ng/µl
P739 pSB1C3_001_VP2/3_capins_587_KO_Bap_clone2 c = 110,2 ng/µl
P740 pSB1C3_001_VP2/3_capins_587_KO_Bap_clone3 c = 71,46 ng/µl
P741 pGGTBT7-ZEGFR:1907_Middlelinker_EGFP_His c = 115,4 ng/µl

140. labday 05.10.2010

Site-directed mutagenesis in pSB1C3_mGMK_TK30 construct

Investigator: Bea

Comment: Since we are still waiting for the ordered TK30, idea was to mutate the PstI site in the TK30 region. After mutating the PstI it is ready for submitting. Addtionally the ordered and received sr3ß can be subcloned.

Protocol using the QuickChange Ligthning Kit from Stratagene:

https://2010.igem.org/Image:Freiburg10_SDM_PstI_TK30_05_10.tif

The follwoing PCR was used:

• 95 °C 2'
• 95 °C 20"
• 60 °C 1'
• 68 °C 2'
• Goto 2 repeat 17
• 68 °C 5'

After the PCR program was conducted, I added 1 µL of DpnI provided with the Kit to each sample and incubated it for 10 minutes.
For transformation XL-10 Gold cells with 2µL beta-mercaptoethanol have been used and plated on agar plates containing chloramphenicol.

Cellculture: Bad news

Something happened to our virus-production cell line AAV293.

Nearly all AAV293 cells are dead.

The whole Loop-Insertion Transfection from 3.10 is lost, our actual culture flasks aswell. We dont know exactly the cause of this cellular mass mortality. Maybe someting is wrong with the new FCS-stocks.

Repetition of pCerulean_VP1up_NLS_DARPin

Investigators: Achim

• The Test Digestion (1.10.) of the last attempts clones didn't look convincing. We sent clone 1 for sequencing yesterday, but we didn't recieve any results yet. That's why I decided to repeat the experiment today, in case results are negative.

• Details: See first run from 28.9.

Prep. Gel:

Harvest of viral stocks

Investigators:

Number of viral stocks: 4

• mVenus standard stock 10 x cm R/C: P468² plates => Harvest in 2 50 ml Falcons, four times freeze thaw centrifugation step with 2500g for 10 min
• TKGMK stock 10 x cm² plates R/C: P468 => Harvest in 2 50 ml Falcons, four times freeze thaw centrifugation step with 2500g for 10 min
• viral particles with GOI (mVenus) missing HGH one 6well plate => Harvest in 1 50 ml Falcon, four times freeze thaw centrifugation step with 2500g for 10 min
• viral particles with GOI (mVenus) missing beta globin one 6well plate => Harvest in 1 50 ml Falcon, four times freeze thaw centrifugation step with 2500g for 10 min
• viral particles with R/C missing HSPG binding motif one 6well plate => Harvest in 1 50 ml Falcon, four times freeze thaw centrifugation step with 2500g for 10 min
• viral particles with new standard R/C (intact HSPG binding motif) one 6well plate => Harvest in 1 50 ml Falcon, four times freeze thaw centrifugation step with 2500g for 10 min

Motivation:
The two new standard vectors are from now on called Control Vectors, to get valide data. The TKGMK Stock will be used for the MTT-ASSAY.

Repetition of Cloning lITR_phTERT_beta-globin_mGMK_TK30 into pSB1C3_hGH_rITR

Investigator: Anna

Comment: Second approach of Cloning lITR_phTERT_beta-globin_mGMK_TK30 into pSB1C3_hGH_rITR, first one didn't work (see labday 01.10.).

Vector name:

• pSB1C3_hGH_rITR (P186)

c= 129,6 ng/µl

Insert name:

• pSB1C3_lITR_phTERT_beta-globin_mGMK_TK30 (P673)

c= 266,4 ng/µl

components	volume for Pp728 /µl	volume of P673 /µl
DNA	11,6	7,5
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme XbaI	1	-
Enzyme EcoRI	1	1
Enzyme SpeI	-	1
H2O	2,4	6,5
Total volume (e.g. 15,20,25,30 µl)	20	20

0,4 g Agarose, 50 ml TAE (0,8%), 3 µl GELRED , at 115 Volt

Gel extraction:
Was performed according to the standard protocol.

	rITR_hgH	lITR_phTERT_betaglobin_mGMK_TK30
Expected size of fragment	2690 bp	3045 bp
DNA-concentration [ng/µl]	37,4	19,81

T4 Ligation:

volume of vector	1,1 µl
volume of insert	6,9 µl

Transformation:
Was done following the standard protocol using BL21 cells.

Seeding HT1080 and AAV431 for transduction

• 3*6well plates HT1080
• 3*6well plates A431

for transduction with following viral stocks:

• mVenus Control Vector to quantify the other stocks
• mVenus without beta-globin
• mVenus without HGH
• mVenus in viral vectors without HSPG-Binding-site(P667)
• mVenus in viral vectors with HSPG-Binding-site, the new state-of-the-art-R/C (P668)

Cloning of pSB1C3_lITR_phTERT_beta-globin_CD and pSB1C3_lITR_CMV_beta-globin_CD

Investigator: Anissa

Vector name:

• pSB1C3_lITR_phTERT_beta-globin (p730)
• pSB1C3_lITR_CMV_beta-globin (P729)

Insert name:

• VB:pSB1C3_CD(P690)

components	volume of P730 /µl	volume of P729 /µl	volume of P690 /µl
DNA	12	4,1	9,9
BSA (10x)	2	1,5	2
Buffer 4 (10x)	2	1,5	2
Enzyme AgeI	1	1	-
Enzyme NgoMIV	-	-	1
Enzyme PstI	1	1	1
H2O	1	5,9	4,1
Total volume (e.g. 15,20,25,30 µl)	20	15	20

Gel:
for vectors and insert :
0,5 g Agarose, 50 ml TAE (1%), 3 µl GELRED , at 110 Volt

Gel extraction:
Was performed according to protocol.

T4 Ligation:

• Volume vector P729: 1,39 µl
• Volume insert: 6,61 µl

• Volume vector P730: 3,55 µl
• Volume insert: 4,45 µl

Transformation:
Was performed according to standard protocol using BL21 cells.

Repetition of the test-digestion of p714,p715,p719,p720,p721,p724 and p726

Investigator: Anissa

• pSB1C3_lITR_CMV_beta-globin_mCherry: Cut with EcoRI, PstI & NdeI
  • P714 (Lane 1)
  • P715 (Lane 2)
    • Results:Looks good.

• pSB1C3_lITR_phTERT_beta-globin_mCherry: Cut with EcoRI, PstI & SacII
  • P719 (Lane 3)
    • Results:Looks good.

• pSB1C3_lITR_phTERT_beta-globin_CFP_hgh_rITR: Cut with EcoRI, AgeI & PstII
  • P720 (Lane 4)
  • P721 (Lane 5)
    • Results:The expected bands should run at 671 bp,2033 bp and 1855 bp. Sequencing has to be repeated

• pSB1C3_lITR_phTERT_beta-globin_CD: Cut with PstI & EcoRI
  • P724 (Lane 6)
  • P726 (Lane 7)
    • Results:The expected bands should run at 2035 and 2460 bp. The experiment has been repeated already today.

Repetition: Cloning of VP2/3_BAP_HSPG-KO and VP2/3_His_HSPG-KO into pCerulean_Zegfr:1907_Middlelinker and VP2/3_His_HSPG-KO into pCerulean_VP1up_NLS_mVenus

Investigator: Stefan

Comment: Cloning of 587-ko_His and 587-ko_BAP into pSB1C3_001_VP2/3_capins did not work out last time. Since cloning of VP2/3_capins started before sequencing results arrived, this experiment has to be repeated.

Vector name:

• pCerulean_Zegfr:1907_Middlelinker (P408)
• pCerulean_VP1up_NLS_mVenus (P426)

Insert name:

• pSB1C3_001_VP2/3_capins_587_KO_His_clone3 (P734)
• pSB1C3_001_VP2/3_capins_587_KO_Bap_clone1 (P738)

components	volume for inserts (P734 + P738) /µl	volume of P408 /µl	volume of P426 /µl
DNA	14	3	3
BSA (10x)	3	2	2
Buffer 4 (10x)	3	2	2
Enzyme NgoMIV	1	-	-
Enzyme PstI	1	1	1
Enzyme MscI	1	-	-
Enzyme AgeI	-	1	1
H2O	7	11	11
Total volume (e.g. 15,20,25,30 µl)	30	20	20

Gel:
0,4 g Agarose, 50 ml TAE (0,8%), 3 µl GELRED , at 115 Volt

Gel extraction:
Was performed according to protocol.

T4 Ligation:

ligation name	408 + 734	408 + 738	426 + 734	426 + 738
volume of vector	3,81	3,81	3,56	3,56
volume of insert	4,19	4,19	4,44	4,44

Transformation:
Was performed according to standard protocol using BL21 cells.

PCR of VP1-3

Investigator: Kira

Comment: this approach was already repeated at least 2 times, but still even if its not one of the very important constructs, it should be finished by end of the month.

PCR*PCR program:

c(pKEX_VP1)=488 ng/ul
c(pKEX_VP2)=484 ng/ul
c(pKEX_VP2)=485 ng/ul

VP-1 praefix primer: 089 VP-2 praefix primer: 090 VP-3 praefix primer: 091 VP1-3 suffix reg_25: 0120

components	volume in µl
5x Phusion HF buffer	10
10 mM dNTP mix	1
primer_for (1:10 dilution)	2,5
primer_rev (1:10 dilution)	2,5
DNA template (1:100)	0,5
DMSO	0
Phusion polymerase	0,5
H2O	33
Total volume (e.g. 50 µl)	50

The PCR programm for all 3 samples was the same due to the weakest primer, which is VP-1 praefix primer

Cycles	Temperature	Time
	98°C	30 sec
10x	98°C	10 sec
	60°C	25 sec
	72°C	1 min 6 sec
20x	98°C	15 sec
	72°C	1 min 31 sec
1x	72°C	5 min
Hold 4°C

1% agarose gel

The gel shows only the primer bands on the bottom of the gel --> PCR failed again. Its going to be repeated tomorrow.

141. labday 06.10.2010

Cellculture

Investigator Patrick
Not only the 293 cells look bad. The A431 cells and the HT1080 cells die, too. There is no contamination detectable. Maybe there is something wrong with the DMEM because the now 100 % serum-free AAV293 cells dont die.

Transduction of HT1080 and A431 cells

The cells are not adherent so no transduction was performed.

Sequence analysis of pSB1C3_CD

Investigator: Bea

Comment: After test digestion revealed positive results, we sent one clone for sequencing (P690) with VF-2 and VR-2 primers. The tube numbers are: SB_1 and SB_2.

Results:

• Prefix looks well. Alle restriction sites can be found in the prefix RFC25.
• Suffixlooks well. Alle restriction sites can be found in the suffix RFC25.
• BUT: There seems to be a PstI recognition site within the sequence. Therefore the site-directed mutagenesis needs to be repeated.

Site-directed mutagenesis of pSB1C3_CD

Investigator: Bea

Comment: Since the sequence analysis revealed that the PstI restriction iste within the CD is NOT removed I prepared another Quickchange in order to mutate the PstI site.

Protocol:

The following PCR was used:

• 95 °C 2'
• 95 °C 20"
• 60 °C 10"
• 68 °C 1'45"
• Goto 2 repeat 17
• 68 °C 5'

After the PCR program was conducted, I added 1 µL of DpnI provided with the Kit to each sample and incubated it for 10 minutes at 37°C.
For transformation XL-10 Gold cells with 2µL beta-mercaptoethanol have been used and plated on agar plates containing chloramphenicol.

Sequencing analysis

Investigator: Stefan
Comment:
Sequencing reults of pSB1C3_CMV_Z_EGFR:1907_VP2/3_CapIns (P679), pSB1C3_CMV_Z_EGFR:1907_VP2/3_CapIns_HSPG-ko (P684), pSB1C3_001_VP2/3_587_HSPG-ko_His(P734) and pSB1C3_001_VP2/3_587_HSPG-ko_BAP(P738). In P679 and P684, CMV_Z_EGFR:1907 was cloned in front of VP2/3, in P734 and P738, 587_HSPG-ko_His/BAP was cloned into the 587 loop.

Test Digestion of pSB1C3_CMV_DARPin_MiddleLinker_VP2/3_insCap and pSB1C3_CMV_DARPin_MiddleLinker_VP2/3_HSPG-KO

Investigator: Hanna
Comment: Besides the Affibody we also want to test and characterize the DARPin E01 as a targeting motif for EGFR over expressing tumor cells. The day before yesterday a 3 fragment ligation was performed with the CMV promoter, DARPin and pSB1C3_VP2/3_insCap/pSB1C3_VP2/3_HSPG-KO.
2 clones were picked from each approach and preped today.

TEST DIGESTION:

• DNA: 2 µL
• Buffer 3: 1 µL
• BSA (10x): 1 µL
• XbaI: 0.5 µL
• BmgBI (cuts in the DARPin sequence): 0.5 µL
• H2O: 5 µL

Incubation: 2 hours.

Conclusion: Test digestion looks well: Expected fragments = 756 bp and 4409 bp.
Two samples were sent for sequencing to GATC using the CMV-F primer.

Repetition: Cloning of CFP into pSB1C3_lITR_phTERT_beta-globin and hgH_rITR into pSB1C3_lITR_CMV_beta-globin_mCherry and into pSB1C3_lITR_phTERT_beta-globin_mCherry

Investigator: Stefan

Comment:

Vector name:

• pSB1C3_lITR_phTERT_beta-globin (P437)
• pSB1C3_lITR_CMV_beta-globin_mCherry (P715)
• pSB1C3_lITR_phTERT_beta-globin_mCherry (P719)

Insert name:

• pSB1C3_CFP (P666)
• pSB1C3_hgH_rITR (P728)

components	volume for inserts (P666 + P728) /µl	volume of vectors P437 + P715 + P719 /µl
DNA	10	4
BSA (10x)	2	2
Buffer 4 (10x)	2	2
Enzyme PstI	1	1
Enzyme XbaI	-	1
Enzyme SpeI	1	-
H2O	4	10
Total volume (e.g. 15,20,25,30 µl)	20	20

Gel:
0,4 g Agarose, 50 ml TAE (0,8%), 3 µl GELRED , at 115 Volt

Gel extraction:
Was performed according to protocol.

T4 Ligation:

ligation name	437 + 666	715 + 728	719 + 728
volume of vector	5,08	5,13	5,34
volume of insert	2,92	2,87	2,66

Transformation:
Was performed according to standard protocol using BL21 cells.

Biotinylation of the monoclonal IgG antibody A20

The biotinylation of the A20 antibody that recognizes the assembled virus was performed with a biotinylation Kit purchased from Dojindo.

• The first biotinylation reaction was performed according to the protocol with 150µg of the purified antibody but resulted in not detectable protein concentrations.
• The biotinylation reaction was repeated for a second time with 200µg and resulted in satisfying protein concentrations.
  • Successful biotinylation has to be tested in an other experiment.

Repetition of VP1-3 PCR

Investigator: Kira
PCR program:

c(pKEX_VP1)=488 ng/ul
c(pKEX_VP2)=484 ng/ul
c(pKEX_VP2)=485 ng/ul

VP-1 praefix primer: 089 VP-2 praefix primer: 090 VP-3 praefix primer: 091 VP1-3 suffix reg_25: 0120

Regarding the primer sequences, DMSO will be added to the PCR samples.

components	volume in µl
5x Phusion HF buffer	10
10 mM dNTP mix	1
primer_for (1:10 dilution)	2,5
primer_rev (1:10 dilution)	2,5
DNA template (1:100)	0,5
DMSO	2
Phusion polymerase	0,5
H2O	31
Total volume (e.g. 50 µl)	50

The PCR programm for all 3 samples was the same due to the weakest primer, which is VP-1 praefix primer

Cycles	Temperature	Time
	98°C	30 sec
10x	98°C	15 sec
	59°C	25 sec
	72°C	1 min 11 sec
20x	98°C	15 sec
	72°C	1 min 36 sec
1x	72°C	5 min
Hold 4°C

1% agarose gel
File:Freiburg10 VP1-3 PCR.jpg

Digestion of plasmid backbone:

pSB1C3_001 is used as backbone

Components	vector Volume/µL
DNA	3,0 µl
BSA (10x)	2 µl
Buffer no. 4 (10x)	2,0 µl
Enzyme 1 AgeI	1,5 µl
Enzyme 2 SpeI	1,0 µl
H2O	10,5 µl
Total volume	20

incubation @ 37 C for approx. 2 h

1% agarose gel
File:Freiburg10 digestion-pSB1C3 001.jpg

Digestion of PCR product:

Components	PCR product Volume/µL
DNA	30,0 µl
BSA (100x)	4,5 µl
Buffer no. 4	4,5 µl
Enzyme 1 NgoMIV	1 µl
Enzyme 2 SpeI	1,0 µl
H2O	4 µl
Total volume	45

incubation @ 37 C for approx. 2 h

ligation with T4 ligase was performed over-night

Cloning of Rep into Rep52 and Rep78

Investigator: Kira
Comment: In order to perfom PCR, we have to clone the ordered Rep gene into Rep52 and Rep78 backbones.

Regarding the activity conditions of the enzymes, digestion was performed in 2 steps.

Components	insert	Rep78	Rep52
DNA	3 µl	2 µl	7 µl
BSA (100x)	2 µl	2 µl	2 µl
Buffer no. 3	2,0 µl	2,0 µl	2,0 µl
Enzyme SwaI	1,0 µl	1,0 µl	1,0 µl
H2O	12 µl	13 µl	8 µl
Total volume	20

incubation @ 25 C for approx. 2 h
Dephosphorylation was performed because of the blunt cleavage. PCR phosphorylation followed in order to get rid off the buffer because Buffer 3 is not appropriate for further digestion. after PCR phosphorylation:
c(pMA_RC-insert)= 21,75 ng/ul c(rep52)= 75,82 ng/ul c(rep78)= 2,47 ng/ul

Components	insert	Rep78	Rep52
DNA	30 µl	30 µl	30 µl
BSA (100x)	0 µl	0 µl	0 µl
Buffer no. 2	4,5 µl	4,5 µl	4,5 µl
Enzyme HindIII	1,0 µl	1,0 µl	1,0 µl
H2O	9,5 µl	9,5 µl	9,5 µl
Total volume	45

incubation for 2h at 37C

File:Rep52&Rep78.jpg

the gel shows that Rep78 backbone got lost.. Regarding the concentration, which was measured after PCR purification it might be possible --> digestion of Rep78 will be repeated tomorrow, while Rep52 is ready for ligation.

142. labday 07.10.2010

DARPin VP2 Fusion: Sequencing results

Investigator: Hanna

COMMENT: The DARPin was fused with the Middle Linker to the VP2/3 BioBrick and cloned into the pSB1C3 backbone. Yesterday's test digestion looked well, so one clone of the VP2/3_insCap and one clone of the VP2/3_HSPG-KO construct was sent for sequencing.

CONCLUSION: Sequencing looked well: 3 fragment ligation was successful - because the CMV-F primer was used for sequencing, the CMV promoter was successfully inserted. As shown in the alignments also the DARPin was inserted. This is the first time that the DARPin was sequenced - thus the original sequence must also be OK!
These two constructs are finished and are ready to be tested in cell culture via qPCR, ELISA,... and can be stored in our BioBrick Box for submitting.

Repetition of cloning of ordered Rep into Rep78

Investigator: Kira
Comment: Because the gel from yesterday did not show any bands in the Rep78 line, I desided to repeat this approach but to use more DNA, in order to be able to continue with the second digestion (see labday 06.10.2010)

The same procedure but with 7 ul Rep78 (c=556 ng/ul). After the first digestion, dephosporylation and PCR purification were performed and DNA was measured.

As a control, the ordered Rep was used again.

c(p190)= 28 ng/ul
c(Rep78)= 6,90 ng/ul

the second digestion as performed despite the low concentration.

File:Freiburg10 2010-10-07.jpg

The gel shows once again no detectable DNA of Rep78.

Transformation of VP1-3 & pSB1C3_001 and p190 &Rep52

Investigator: Kira

The transformation was performed according to the standard protocol with BL21. Compared to VP1-3 transformed cells, Rep52 cells revealed no visible pellet after centrifugation, thus 300 ul of the cells suspension was plated.

Test digestion of different constructs

Investigator: Anna

Gel1_Part1: The 453 constructs were cut with BamHI and SspI, the 587 constructs with SalI and PvuII. The inserts were cloned into pSB1C3_RepCap_p5tatless.

All of the following constructs were cut with EcoRI and PstI:

Gel1_Part2:

Gel2:

143. labday 08.10.2010

Mini-Prep and test digestion of several constructs

Investigator: Stefan

Comment: Mini-Preps were performed according to protocol:

Glycerol stocks were prepared:

• B641 pSB1C3_lITR_phTERT_beta-globin_CFP clone 1
• B642 pSB1C3_lITR_phTERT_beta-globin_CFP clone 2
• B643 pSB1C3_lITR_CMV_beta-globin_mCherry_hgH_rITR clone 1
• B644 pSB1C3_lITR_CMV_beta-globin_mCherry_hgH_rITR clone 2
• B645 SB1C3_lITR_phTERT_beta-globin_mCherry_hgH_rITR clone 1
• B646 pSB1C3_lITR_phTERT_beta-globin_mCherry_hgH_rITR clone 2

Mini-Prep was performed according to standard protocol:

• P791 pSB1C3_lITR_phTERT_beta-globin_CFP clone 1 c = 244.3 ng/µl
• P792 pSB1C3_lITR_phTERT_beta-globin_CFP clone 2 c = 214.3 ng/µl
• P793 pSB1C3_lITR_CMV_beta-globin_mCherry_hgH_rITR clone 1 c = 209.2 ng/µl
• P794 pSB1C3_lITR_CMV_beta-globin_mCherry_hgH_rITR clone 2 c = 262.4 ng/µl
• P795 pSB1C3_lITR_phTERT_beta-globin_mCherry_hgH_rITR clone 1 c = 234.7 ng/µl
• P796 pSB1C3_lITR_phTERT_beta-globin_mCherry_hgH_rITR clone 2 c = 207.2 ng/µl

Test digestion:

Comment:Additionally, P771 and P781 from yesterday's Mini-Prep were digested again.

Components	P791 + P792 / µl	P793 - P796 / µl	P771 / µl	P781 / µl
DNA	1,5	1	3	7,7
Buffer 4	1	1	1	1
BSA (10x)	1	1	1	1
PstI	0,3	0,3	0,3	0,3
EcoRI	0,3	0,3	-	-
BpmI	0,3	-	-	-
H2O	5,6	6,4	4,2	-
Total volume	10	10	10	10

Results:

Comment:Samples P791 to P796 perform like expected, they can be used for further cloning or testing in cell culture. P771 show strange bands, a test PCR will be performed to verify successful cloning. P781 does not show any DNA at all like last time. A new SDm will be performed for pSB1C3_mGMK_TK30 (P675).

Test-PCR of pSB1C3_lITR_phTERT_beta-globin_mGMK_TK30_hgH_rITR

Investigator: Stefan

Comment: Test digestion showed strange results (an additional band at 500bp which does not fit any expectations), therfore an additional test-PCR was performed to verify successful cloning of the complete constructs.

Components	positive control / µl	negative control / µl	sample P771 / µl
5x Phusion HF buffer	10	10	10
10mM dNTP mix	1	1	1
Primer for (1:10 dilution)	O107 2,5	O29 2,5	O29 2,5
Primer rev (1:10 dilution)	O108 2,5	O191 2,5	O191 2,5
DNA template	1 (1:100)	1 (1:100)	1 (1:100)
DMSO	1	1	1
Phusion Polymerase	0,5	0,5	0,5
H2O	32,5	32,5	32,5
Total volume	50	50	50

Gel:
0,5 g agarose, 50 ml TAE (1%), 115V, 50 minutes

Comment: Test PCR showed successful cloning of lITR_phTERT_beta-globin_mGMK_TK30 into pSB1C3_hgH_rITR. SDM to remove PstI in TK30 can be performed.

Trafo evaluation of VP1-3 and Rep52 constructs

Investigator: Kira
VP1-3 contain lots of colonies, while Rep52 plate is empty

Repetiton: Site-directed mutagenesis in pSB1C3_mGMK_TK30 construct

Investigator: Stefan

Comment: The first try to remove the PstI restriction site delivered no plasmid DNA, so another approach needs to be started.

Protocol using the QuickChange Lightning Kit from Stratagene:

Ingredients:

Ingredients	Volume / µl
10x reaction buffer	2,5
dNTP	0,5
forward primer: O191	0,69
reverse primer: O192	0,71
DNA Template	5
QuikSolution Reagent	0,75
QuikChangeLightning Enzyme	0,5
H2O	14,35
Total volume	25

The following PCR program was used:

• 95 °C 2 minutes
• 95 °C 20 seconds
• 60 °C 1 minute
• 68 °C 2 minutes
• Goto step 2 repeat 17 times
• 68 °C 5 minutes

Digestion using DpnI:
To digest methylated and hemi-methylated DNA, 1 µl of DpnI was added and the mixture was incubated for 10 minutes at 37 °C.
Transformation:
Since XL-10 Gold cells delivered a bacteria lawn on the plates, this time XL1b cells were used.

144. labday 09.10.2010

Mini-Prep of pSB1C3_CD_SDM-PstI

Investigator: Stefan

Comment: Mini-Prep was performed according to standard protocol.

Glycerol stocks were prepared:

• B647 = pSB1C3_CD_SDM-PstI clone 1
• B648 = pSB1C3_CD_SDM-PstI clone 2

Mini-Prep was performed according to standard protocol:

• P797 = pSB1C3_CD_SDM-PstI clone 1 c = 8,2 ng/µl
• P798 = pSB1C3_CD_SDM-PstI clone 2 c = 7,1 ng/µl

Comment: Since Mini-Prep from XL-10 cells yielded that little plasmid, a re-trafo will be performed using BL21 cells.

Transformation:
A 1:10 dilution of both plasmids was prepared and 1 µl was added to BL21 cells.
Transformation was performed according to standard protocol. Cells were plated on agar plates containing chlorampenicol.

Preparation of competent cells and Test-Trafo

Investigator: Stefan

Preparation of BL21 (red line) and XL1-blue (green X) cells was performed according to standard protocol.
Do not use cells until further notice!

Test PCR of qPCR primer for phTERT

Investigator: Bea

Comment: The GOI which is flanked by the ITRs and encapsidated in the capsid is the mGMK_T30 driven by the pHTERT promoter which is only active in several tumor cells. Since we have never tested the primers if they work I wanted to do that. This time I tried to use the TAQ polymerase which we received from Peqlab. Since I could not find a standard protocol for the PCR provided by peqlab I tried to compare several manuals and combine them.

Protocol:

[[Image:|thumb|center|700px]]
I checked the protocol today (10.10) and recognized that I added accidentially to much buffer to the PCR-Mix. Maybe this could be another explanation for the negative results of the PCR.

The following PCR was used:

• 94 °C 3'
• 94 °C 30"
• 50 °C 30"
• 72 °C 10"
• Goto 2 repeat 17
• 68 °C 7'

Result:
Unfortunately the expected PCR product with a size of 182 bp could not be detected as it can be seen in the agarose gel. I can not say if the protocol needs to be modified or if the primer pair did not anneal adequatly. Therefore, I am going to repeat the PCR tomorrow by using the Phsuion polymerase for checking the results.

Cloning of p40 in front of VP123

Investigator: Bea

Comment: We want to test the promoter strenth of several promoters (CMV, P40, p5, p5tataless) and compare them in order to provide the possibility of choosing the proper promoter for each experiment and to titrate the plasmids during transfection. Therefore, the p40 promoter needs to be fused in front of the VP123 construct in order to compare the CMV and the p40 promter

Protocol:

[[Image:|thumb|center|700px]]

The following results of the agarose gel can be seen. The fragments were cut out and a gel extraction has been performed:

For transformation BL21 cells have been used and plated on agar plates containing chloramphenicol.

Site-directed mutagenesis of pSB1C3_leftITR_phtert_betaglobin_mgmktk30_hGH_rITR

Investigator: Bea

Comment:

Protocol:

[[Image:|thumb|center|700px]]

The following PCR was used:

• 95 °C 2'
• 95 °C 20"
• 60 °C 10"
• 68 °C 2'50"
• Goto 2 repeat 17
• 68 °C 5'

After the PCR program was conducted, I added 1 µL of DpnI provided with the Kit to each sample and incubated it for 10 minutes at 37°C.
For transformation XL-1 cells have been used because the bacterias of the last site-directed mutageneis approaches using XL-10 cells showes extensive grwoth (bacterial lawn). I plated on the transformaned cells on agar plates containing chloramphenicol.

Cloning HSPG-KO_empty into pSB1C3-001_pCMV_[AAV2]VP123_453_RGD and pSB1C3-001_pCMV_[AAV2]VP123_453_Z34C

Investigator: Achim

• In order to obtain transduction data for our targeting approaches, we still need constructs with RGD/Z34C in the 453 loop as well as HSPG_KO_empty in the 587 loop.

• I digested pSB1C3_HSPG-KO_empty (P611) as well as pSB1C3-001_pCMV_[AAV2]VP123_453_RGD (P634) and pSB1C3-001_pCMV_[AAV2]VP123_453_Z34C (P641)with BamHI and PvuII and ligated the HSPG-KO_empty motive into both vectors.

• Digestion:20µl,Buffer 4, BSA, 1µl enzyme, 37°

• • VB:pSB1C3_001_587_KO_empty (P611)
    • c=160 ng/µl ->14 µl
  • pSB1C3-001_pCMV_[AAV2]VP123_453_RGD (P634)
    • c=239 ng/µl (1:10 dilution of midiprep)->5 µl
  • pSB1C3-001_pCMV_[AAV2]VP123_453_Z34C (P641)
    • c=229 ng/µl (1:10 dilution of midiprep) -> 5µl

• Dephosphorylation:

• Prep gel:

• Ligation: T4

Cellculture

Investigator Patrick

Transduction of HT1080 and A431. Yesterday 3 6-well plates of HT1080 and A431 were seeded with 200.000 cells into each well. The transductions were performed with the following AAV2s

• mVenus without beta-globin
• mVenus without HGH
• mVenus HSPG KO
• mVenus standard
• mVenus new standard

Expected results:

• mVenus without beta-globin: beta globin is said to improve the expression therefore we expect a worse mVenus expression compared to the standard AAVs.
• mVenus without HGH: HGH is responsible for the mRNA polyadenylation of the virus so we expect expect a worse mVenus expression compared to the standard AAVs, too.
• mVenus HSPG KO: the primary AAV2 receptor (the HSPG receptor) was knocked out therefore we expect a worse tranduction rate (about 0,3 to 0,4 of the standard transduction rate, assuming that there are HSPGs on the HT1080 and A431 cell surface). The worse the better.
• mVenus standard: this will be the reference for the other four transduction experiments (no point mutations, GOI: mVenus)
• mVenus new standard: AAV2 with 4 point mutations, inserted rep & cap and "remutated" KpnI restriction site hopefully yiels results similar to the mVenus standard.

145. labday 10.10.2010

Repetition of Test-PCR of qPCR primer for phTERT

Investigator: Bea

Comment: The GOI which is flanked by the ITRs and encapsidated in the capsid is the mGMK_T30 driven by the pHTERT promoter which is only active in several tumor cells. Since we have never tested the primers if they work I wanted to do that. For several reason I decided to use the Phusion polymerase to perform the PCR. First, we are familiar with the handling of this polymerase and have a protocol which we already used several times and second, since I could not find any standard protocols for the TAQ-polymerase provided by PeqLab, as mentioned yesterday, I will rely on the Phusion polymerase.

Protocol:

[[Image:|thumb|center|700px]]

New XL1b and BL21 cells ready to use!

Investigator: Stefan

Cloning Super Constructs and VP2 N-terminal Fusion_ HSPG-KO constructs into pSB1C3_001_CMV or pSB1C3_CMV

Investigator: Hanna

Comment: In order to send our final VP2 N-terminal Fusion constructs with HSPG konock down and our super constructs to the registry, they need to be cloned into the pSB1C3 backbone.
We would prefer sending them in the pSB1C3_001 plasmid, because it does its ViralBricks restriction sites were deleted. Therefore one can cut out the 587_KO ViralBrick and replace it by any ViralBrick of interest.
Because test digestion of pSB1C3_001_CMV didn't show any clear results, I will digest both clones and in addition to that pSB1C3_CMV.

Incubation: 2 h, 37°C

Midi-Prep

Investigator: Chris W.

Midi-Prep of:

pCerulean_VP1up_NLS_Zegfr:1907_VP2/3-Capins clone 2 =P799 =B401
pSB1C3_CMV_DARPin_MiddleLinker_VP2/3_insCap clone 2 =P800 =B595
pSB1C3_CMV_DARPin_MiddleLinker_VP2/3_HSPG-KO clone 1 =P801 =B596
pSB1C3_left-ITR_phTERT_beta-globin_mGMK_TK30_hGH_right-ITR clone 1 =P802 =B622

The Midi-Preps were performed according to the standard protocol yielding the following concentrations:

plasmid-no.	P799	P800	P801	P802
concentration (ng/µl)	662,8	911,3	495,6	673,9

Checking trafo plates of Viralbrick approaches and SDM of pSB1C3_leftITR_phtert_betaglobin_mgmktk30_hGH_rITR and P40_VP123

Investigator: Bea

Comment: Unfortunately, no cells grew on the agar plates containing cm. Therefore, we repeat the Trafo ones again and plate them on new agar plates hoping that colonies will grow over night.

Preparations for ELISA

Investigator: Volker M.

Two 96-well plates that were coated with 200µg A20 antibody per well for 48h at 4°C were washed three times with 200µl PBST Buffer and incubated over night at 4°C with 300µl PBST + 0.2 % BSA.

As a preparation 4 liters of PBS buffer were prepared.