Brandon:LabNotes/Project1/2015-3-23
Guanidine HCl after transposition, taq2X and IVT on beads, 100 cell samples[edit]
- Did 6/4/2014 Guanidine HCl with taq2X and IVT on beads awhile ago and it worked, and didn't try it again. will try it with 100 cells samples using t7top2 with 5X tn5-059.
- where control cell samples did not work when using AMPURE beads.
- In 4/30/2014 Testing pooling and purification with AMPURE beads
- In 3/11/2014 Testing pooling and purification with AMPURE beads
- In 5/21/2014 Pooling and purification with AMPURE beads on FACS sorted 10 cell samples
- In 5/23/2014 pooling and purification with ampure beads, IVT not run on beads
- using undiluted transposase this time, all use 1000 cells.
- experiment using guanidine HCl that worked Guanidine HCl after transposition, or other steps. taq2X on beads, IVT and AMPURE beads
- 9/10/2014 R4 testing, guanidine HCl on beads guanidine treatment then ampure beads works well
- 9/15/2014 figuring out guanidine found out guandine HCl purification with beads works well.
- 3/11/2015 guanidine HCl treatment with EtOH purification, with taq2X, IVT after used wrong transposon, disregard
- 3/16/2015 guanidine HCl treatment with EtOH purification, with taq2X, IVT after Round 2 didn't really work for pooling samples and 500 cell samples
- when searching "guanidine hcl and ampure beads"
- "Use of SPRI instead of spin filter for tagmentation cleanup. To decrease manual intervention, a magnetic bead‐based method for purifying the tagmentation reactions was implemented. In order to dissociate the tagmentase enzyme from the DNA, guanidine HCl is added to a net concentration of 4 M. Two sequential additions of AMPure bead reagent are effective at purifying the DNA from the rest of the tagmentation reaction components, as shown in Figure 3." http://www.perkinelmer.com/pdfs/downloads/GDE_Nextura_JANUS_NGS_EXpress.pdf
- This method has already been validated on an automated system, and should work for us.
- They also perform 2 step beads purification, and that will be tried too.
Add .8X uL beads to sample Inucubate for 10 minutes Incubate on magnet for 5 minutes remove supernatent Add 1.8X uL beads (1.8X the original volume) Proceed with incubation, magnet and EtOH washing
- The method of using guanidine HCl after tagmentation to denature Tn5 was also also done in this nature protocol Tagmentation-based whole-genome bisulfite sequencing
Before starting protocols[edit]
1. Check if have enough reagents etc for the protocol
- lysis buffer
- sc1 transposomes
- custom 3' transpson
- IVT reagents
- cells etc
- 5X, 2X taq polymerase
- Zymo DNA clean and concentrator
- 2. Samples
samples Transposase is undiluted. 1X concentrated 1. t7-top2, 5X tn5-059, 100 cells rep1 2. t7-top2, 5X tn5-059, 100 cells rep2 3. t7-top2, 5X tn5-059, 1000 cells 4. t7-top2, 5X tn5-059, NTC 5. t7-top2, 5X tn5-059, 6 ng pure DNA
IVT Protocol[edit]
- If need to make more transposome, do first 2 steps. If not goto step 3.
Generation of sc1-T7iBR-IdxXX transposomes
1. annealing of ME sequence to T7 transposon sequence
- a. Make 100 uM stock solution of sc1-T7iBR-IdxXX and sc1-T7tspn-NoP-bot.
- b. Incubate 2.5 uL of each oligo (100uM) with 20 uL EB buffer at 95C for 1 minutes. Oligo's now at 10 uM in 25 uL.
- c. cool to RT at 0.1 C/s
2. transposome complex generation, run controls!!!
- add the below components into one tube and incubate for 20 minutes at RT
1. Add 0.5 uL of 100% sterile glycerol to tube 2. Add 0.5 uL of annealed transposon to the 100% sterile glycerol and mix well 4. Add 1.0 uL of DILUTED Ez-TN5 transposase to well.
- store at -20, is good for a year
Generation of custom barcode (3' side of fragments) nextera transposome
1. annealing of ME sequence to Nextera transposon sequence
- a. Make 100 uM stock solution of (NXTA_ME_BOT, "pMENTS") and (NXTA_ME_B, "B-METS").
- b. Incubate 5 uL of each oligo (100uM) with 40 uL EB buffer at 95C for 2 minutes. Oligo's now at 10 uM in 50 uL.
- c. cool to RT at 0.1 C/s
2. transposome complex generation, run controls!!!
- add the below components into one tube and incubate for 20 minutes at RT
1.25 uL of annealed Nextera transposon 1.25 uL of 100% sterile glycerol 2.50 uL of Ez-TN5 transposase
- store at -20, is good for a year
3. Prepare samples, lyse cells with lysis buffer
CELL WASHING - (wash cells with PBS)
- 1. count cells, spin down all cells at 250-500 g for 5 minutes
- 2. wash with 1X PBS, centrifuge 250-500 g for 5 minutes, resuspend to XX cells/uL
- 3. Count cells again, aliquot cells to sample tubes
CELL LYSIS
- 1. dilute Lysis Buffer (LB) to 2X, or as needed (from 10X stock)
- 3. add LB to cell aliquots, mix briefly (mineral oil optional)
- 4. transposition ready
LYSIS BUFFER NOTES
- Lysis buffer is: 10ml 10X lysis buffer (LB, 100mM Tris.Hcl pH 7.5, 100mM NaCl, 30mM MgCl2, 1% NP40, Crawford et al. PNAS 2003) in nuclease free H2O.
4. transposition reaction Add all components and incubate at 37C FOR 30 MINUTES
1.0 uL 5X Custom Tagmentation buffer 2.0 uL lysed cells/pure genomic DNA 1.0 uL T7 transposomes (MAKE SURE TO ADD LAST) (5X diluted) 1.0 uL N-H2O ___________ 5.0 uL total solution
5. Bring to 15 uL with N-H2O. Add 15 uL 8M guanidine HCl for a total of 30 uL.
- If using beads next add 1.8X (54 uL) beads per sample
ELUTE IN 9.6 or 12 uL DEPENDING, leave beads in solution
6. Fill in reaction
- Add 2.4 uL of 5X taq polymerase or 3.0 uL of taq2X. Run at 72C for 3 minutes. (same as nextera)
8. Maxiscript (Ambion) T7 Protocol, IVT
- DNA from PCR can be used directly in the MAXIscript Kit without any pretreatment or purification.
a. Thaw 10X Transcription Buffer and ribonucleotide solutions. Store the ribonucleotides (A, C, G, U) on ice, but keep 10X transcription buffer at room temp b. Assemble reaction mixture at room temperature, ADD IN ORDER AND MIX THOROUGHLY!!!! bring to 10 uL with Nuclease free water X uL DNA template (list 1 ug) 2 uL 10X Transcription Buffer 1 uL 10 mM ATP 1 uL 10 mM CTP 1 uL 10 mM GTP 1 uL 10 mM UTP 2 uL T7 Enzyme Mix b. Incubate reactions at 37C overnight for ~16 hours. (>10 uM limiting nucleotide)
9. Clean with Zymo clean and concentrator
- elute samples in 10 uL of N-H2O
- quanitate with Qubit or on TBU gel.
AFTER IVT RNA HAS ALREADY BEEN GENERATED AND CLEANED WITH ZYMO
UPDATE 3/25/2015 CONTINUING TO RNA PROCESSSING TO GENERATE SEQUENCING LIBRARIES
Samples this time:
- sample list
1. index 49, t7-top2, 5X tn5-059, 100 cells rep1 2. index 50, t7-top2, 5X tn5-059, 100 cells rep2 3. index 51, t7-top2, 5X tn5-059, 1000 cells 4. index 52, t7-top2, 5X tn5-059, NTC 5. index 53, t7-top2, 5X tn5-059, 6 ng pure DNA
- Amounts of RNA and water to add for MMLV RT (50 ng RNA)
' | 1200 | 2.5 | total | 50 ng | N-H2O |
1. t7-top2, 5X tn5-059, 100 cells rep1 | 10083.3803 | 23.76248153 | 237.6248153 | 2.104157343 | 7.895842657 |
2. t7-top2, 5X tn5-059, 100 cells rep2 | 9901.370295 | 23.32683831 | 233.2683831 | 2.143453791 | 7.856546209 |
3. t7-top2, 5X tn5-059, 1000 cells | 47608.67142 | 113.5797338 | 1135.797338 | 0.44021938 | 9.55978062 |
4. t7-top2, 5X tn5-059, NTC | 2298.250068 | 5.128675234 | 51.28675234 | 1 uL | 9 |
5. t7-top2, 5X tn5-059, 6 ng pure DNA | 165223.0349 | 395.0911795 | 3950.911795 | 1.01 uL 8xd | 8.987 |
8. single strand synthesis MMLV RT (Clontech)
- Followed protocol for SMART MMLV Reverse Transcriptase
20 uL reaction 1. Add 2.5 uL 20 uM (100 ng total) RANDOM HEXAMERS to RNA sample. Bring to final volume of 12.5 uL with Nuclease free H2O 2. heat the mixture to 70C fo 3 minutes. Immediately cool on ice. 3. Add the following to the reaction. 2 uL 5X first strand buffer 2 uL dNTP mix 2 uL 100 mM DTT 1 uL N-H20 .5 uL SMART MMLV RT and mix (ADD LAST!!!!!) ____ 20 uL total 4. Incuvate first at Room Temperature for 10 minutes. Then incubate at 42C for 60 minutes. 5. Terminate the reaction by heating at 70C for 10 minutes
9. RNase H digestion
- Use .5 Units for 20 uL reaction. Stock is at 5 Units/ul, thus dilute 10X and use 1 uL per reaction.
a. Add 1 uL of 10X diluted Rnase H to the reaction.
b. Incubate for 20 minutes at 37C.
10. Second strand synthesis: Adding sss_NPA_prmr primer and polymerases. Can incubate at higher temps (usually at 16C since RNA is nicked) since sss_NPA_prmr has a high Tm.
a. Add 2.5 uL of sss_NPA_prmr to each reaction. b. Incubate solutions for 2 minutes at 65C. Cool immediately on ice. d. Add polymerases etc to reactions taq2X: Add 5.875 uL, Incubate at 72C for 8 minutes NTC: Just add 1 uL of Klenow exo-
11. Clean DNA with AMPURE beads depending. elute in 20 uL and concentreate. (can also use qiaquick)
- USED AMPURE DNA BEADS AT 1:1.8X RATIO
- add 45 uL N-H2O
- add 135 uL beads per reaction
- elute on 20 uL
can quantitate with Qubit or on TBU gel.
11.5. Eluted DNA into 20 uL per sample, since when eluting in smaller amounts more sample is lost. Thus after elution used vaccum centrifuge commentator to concentrate sample size to ~4-5 uL per sample.
- Also ~4-5 uL per sample is preferred for transposition, which has always been performed in low volume solutions. Additionally less transposome will be needed when doing that.
RAN FOR 16 MINUTES
12. Fragmenting and 3' End tagging with Custom Nextera transposome USED EZ-TN5 AND BUFFER D6, nxta_ME_B
1 uL nextera LMW buffer 2 uL lysed/pure genomic DNA (X ng/pg DNA) X uL Nuclase free H2O 1 uL prepared T7 transposomes (MAKE SURE TO ADD LAST) (if was proportional to shendure would use .625 uL) ___________ 5 uL total solution Incubate at 55C for 6 minutes, cool briefly on ice after
13. Protease digestion of transposase, protease inactivation
To each tube, add: 1 uL Qiagen Protease, for 5 uL reaction 1 uL of .5 for .1 AU final. (stock is 5 AU and diluted 10X. want .5 AU/uL final []) Incubate: 50C 10 minutes, 70C 20 minutes
14. Fill in reaction
- Add 6 uL 2X taq polymerase, run at 72C for 3 minutes. (same as nextera)
15. PCR addition of barcodes MAKE SURE TO USE NEXTERA INDEXES!!!!!
Samples:
- sample list
1. index 49, t7-top2, 5X tn5-059, 100 cells rep1 2. index 50, t7-top2, 5X tn5-059, 100 cells rep2 3. index 51, t7-top2, 5X tn5-059, 1000 cells 4. index 52, t7-top2, 5X tn5-059, NTC 5. index 53, t7-top2, 5X tn5-059, 6 ng pure DNA
KAPA SYBR FAST qPCR mix until saturation, X35 cycles 9 uL Taq2X 2 uL primers, 2 uL F, (T7-top2-PCR-iaf, OR iaf2, iaf3) USED iaf2 2 uL NXTA indexes PCR_R.NXTAInd[XX], SPECIFIC TO EACH SAMPLE 4 uL H2O 1 uL 25X SYBR green 12 uL DNA template (use half RT reaction) _____________ 30 uL KAPA SYBR cycles: 72C 3 m, 95C 30s, (95C for 10s, 63C for 30s, 72C for 3 min) X15, 72C for 3 min, 4C forever
- terminate before curves saturate (usually cycle 6-8)
16. Gel Size selection
- gel size select from 400-800 bp, follow gel size selection protocol
- do not need to include controls.
Results[edit]
- total RNA. Used 1200 intensity for 2.5 ng ladder band since its intensity was a littler higher then the 5 ng band. should be +/- 10 ng then.
' | intensity | ng/ul |
2244.490067 | 5 | |
1200 | 2.5 | |
1. t7-top2, 5X tn5-059, 100 cells rep1 | 10083.3803 | 23.76248153 |
2. t7-top2, 5X tn5-059, 100 cells rep2 | 9901.370295 | 23.32683831 |
3. t7-top2, 5X tn5-059, 1000 cells | 47608.67142 | 113.5797338 |
4. t7-top2, 5X tn5-059, NTC | 2298.250068 | 5.128675234 |
5. t7-top2, 5X tn5-059, 6 ng pure DNA | 165223.0349 | 395.0911795 |
- TBU gel after IVT, Guanidine HCl to remove proteins
File:ZhangLab 2 2015-03-24 14hr 42min-labeled.jpg File:ZhangLab 2 2015-03-24 14hr 44min-invert-labeled.jpg
3/25/2015 UPDATE AFTER PCR ADDITION OF BARCODES
- In total ran for 12 cycles, curves came up later then usual maybe since miscalculated and added less RNA.
- qPCR curves
File:2015-03-25 100 cells test, barcode addition.bmp
- after adding barcodes, TBE gel
File:ZhangLab 2 2015-03-25 18hr 58min-labeled.jpg File:ZhangLab 2 2015-03-25 18hr 59min-labeled.jpg
- gel size selection, 220-800 ish bp
File:ZhangLab 2 2015-03-26 13hr 13min-labeled.jpg
- gel size selection validation
File:ZhangLab 2 2015-03-26 17hr 10min-labeled.jpg
conclusions[edit]
- looks like it gave a decent amount of RNA. maybe try RNA processsing on it and look at seqnecing libraries? then can use on john changs cells.