Team:Johns Hopkins/Notebook/Protocols

DNA Synthesis and Assay Protocols

Gel Extraction (QIAquick)

1. Excise DNA fragment from agarose gel with clean, sharp scalpel.
2. Weigh gel slice in colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel (100mg ~ 100µl)
3. Incubate @ 50C for 10 min.
   • SOLUBILIZE AGAROSE COMPLETELY.
   • To help dissolve gel, vortex tube every 2-3 min during incubation.
4. After the gel has dissolved, check that the color of the mixture is yellow. If not, add 10µl 3M NaOAc. Or just add the NaOAc anyway.
5. Add 1 gel volume of isopropanol to the sample and mix
   • Do only if <500bp or >4kb
6. Place spin column in 2mL collection tube.
7. To bind DNA, apply sample to column. Centrifuge 1 min.
8. Discard flowthrough and place column back in same collection tube.
9. Recommended: Add 0.5mL of Buffer QG to column and centrifuge for 1 min.
10. To wash, add 0.75mL of Buffer PE to column and centrifuge for 1 min.
11. Discard flowthrough and centrifuge for an additional 1 min @ 17900 x g (13000rpm).
12. Place column into a clean 1.5mL microcentrifuge tube.
13. To elute DNA, add 30µL Buffer EB to center of membrane, let column stand for 1 min, then centrifuge for 1 min.

Mini-Prep (QIA)

1. Resuspend pelleted bacterial cells in 250 µL Buffer P1 and transfer to a microcentrifuge tube.
2. Add 250 µL Buffer P2 and mix thoroughly by inverting the tube 4-6 times.
3. Add 350 µL Buffer N3 and mix immediately and thoroughly by inverting the tube 4-6 times.
4. Centrifuge for 10 min at 13,000 rpm in a table-top microcentrifuge.
5. Apply the supernatants from step 4 to the QIAprep spin column by decanting or pipetting.
6. Centrifuge for 30-60s. Discard the flow-through.
7. Recommended: Wash the QIAprep spin column by adding 0.5 mL Buffer PB and centrifuging for 30-60s. Discard flow-through.
8. Wash QIAprep spin column by adding 0.5 mL Buffer PB and centrifuging 30-60s.
9. Discard flow-through and centrifuge for an additional minute to remove residual wash bufffer. **IMPORTANT: Residual wash buffer will not be completly removed unless the flow-through is discarded before this additional centrifugation. Residual ethanol from Buffer PE may inhibit subsequent enzyme reactions.**
10. Ordered List ItemPlace QIAprep column in a clean 1.5 mL microcentrifuge tube. To elute DNA, add 50 µL Buffer EB (10mM Tris-CL, pH 8.5) or water to the center of each QIAprep spin column, let stand for 1 min, and centrifuge for 1 min.

PCR Reactions on Small DNA Pieces

Procedure:

1. Combine the following reagents in one tube:
   • 18uL PCR Platinum Supermix
   • .24uL Forward Primer
   • .24uL Reverse Primer
   • .4uL Target DNA
   • 1.12uL Nuclease Free Water
2. Place tube into Thermal Cycler
3. Program Thermal Cycler with desired Denaturing, Annealing and Extension Temperatures.
   • Example:

    94C for 2 minutes
    94C for 30 seconds (Denaturing)
    55C for 30 seconds (Annealing)
    72C for 1min/kb (Extension)
    Repeat Denaturing, Annealing and Extension at least 24 times.
    Hold at 4C

DNA Digestion

DNA Digestion Mixture:

• 25 μl DNA
• 3 μl Buffer 2
• 1 μl EcoRI-HF
• 1 μl PST1
• 3 μl BSA1

PCR 1.0% Agarose Gel

1. Add .3 grams Agarose to 30mL TAE Buffer in volumetric flask.
2. Stopper volumetric flask with Kim Wipes.
3. Microwave mixture for 1 minute to allow Agarose to dissolve.
4. Prepare BioRad Gel Machine:
   • Place gel stand.
   • Add both gel blocks.
   • Insert comb.
5. Allow mixture to cool down to ~40C.
6. Use micropipetter to seal edges of gel stand with the mixture.
7. Add 3uL Ethidium Bromide to remaining mixture.
8. Mix well.
9. Pour mixture onto gel stand.
10. Cover with Paper Towels and allow to harden.
11. Prepare PCR Reaction tubes:
    • For every 10uL PCR product add 1uL Blue Juice.
    • Mix well.
12. Once gel hardens remove gel blocks and comb.
    • Caution: Remove comb vertically so as not to damage wells.
13. Fill gel machine with TAE buffer till liquid reaches above gel.
14. Load 5uL DNA Ladder.
15. Load 5-10uL samples.
16. Run at 100 Volts for 20-25 minutes.
17. Turn machine off and transfer gel to imaging machine.
18. Position gel and take picture under UV.

QuickChange PCR

From Marty Taylor of the Boeke Lab:

Based on two stage protocol from - W. Wang, B. A. Malcolm, Biotechniques 26, 680 (Apr, 1999). This two-stage protocol allows formation of some of a “hybrid” between WT and mutant, reducing competition between primer and its GC

Design primer to span region to be changed. Depending on the degree of change (single point mutation vs large deletion/insertion) I usually have 15-40nt on either side with perfect match. Order primer and its reverse complement. We have had good luck using Ultramers from IDT up to ~150nt long, haven’t tried anything longer. We do not PAGE purify primers for this application.

For each primer, setup a 25uL reaction (for older PCR machines with 0.5mL tubes, double everything and you may want to extend the annealing/extension times). I usually do a number of these at a time from the same template, so I make a master mix containing everything but primers, aliquot, and then add primers.

1. Template dNA (~25ng) [1 uL from miniprep]
2. 12.5pMol primer [1.25uL] of 10uM stock – be sure to use only one primer each!
3. 5x Buffer [5 uL]
4. dNTPs (2.5mM each) [2 uL]
5. Herculase II [0.5 uL]
6. H2O → 25uL

Control reaction – this is your background! Add 50uL master mix (without primers) to PCR tube and put it on the cycler, identical to the other tubes. DpnI digest transform like the others.

PCR Protocol:

1. Stage 1: setup 2 tubes as above – one for primer, one for its complement – run 2 or 3 cycles
2. Stage 2: combine the two reactions into one, mix well, run for 18 more cycles
   • 95C, 5min
   • [95C, 30sec / 55C, 30sec / 72C (1min/kB total vector+insert)] – 2-3x in stage 1, 18x in stage 2
   • 72C, 10min
   • Extension time – with the new faster enzymes, 30s/kB may be enough, but have had better luck with 1min

DpnI digest – add 0.5uL DpnI (10U/uL) to each 50uL reaction, vortex, incubate at 37°C for 1-3hrs (longer is better if time permits). Be sure to DpnI digest the control and transform and plate it equally. If you think the reaction is a hard one, you can extend the Dpn digestion to reduce background further (or add more enzyme).

Agarose Gel – WASTE OF TIME! This technique often fails to produce enough DNA to see on a gel and still works. So, basically, this step tells you nothing, since you are going to do the transformation whether or not the gel shows you something. I would do a positive control on the transformation long before I run a gel here.

PCR Cleanup – Herculase II reaction mix is incompatible with our standard competent cells (made using Mn/Ca), reducing the efficiency of transformation by at least 3 logs (perhaps due to detergent in the buffer). A quick PCR cleanup solves this problem.

Transform 5uL into a 50uL aliquot of competent cells. We make our own competent cells; for very difficult reactions, we have had success with supercompetent cells, but I haven’t used these since switching to PFU-Ultra. After heat shock, I grow the cells for 1hr in 500uL SOC and plate both 50uL and 450uL. Sometimes the 450uL plate is a lawn; sometimes there are only 10-50 colonies.

Screening – if your control plate is clean (no colonies), I recommend sequencing (or otherwise screening – if your design allows) 3 clones. Usually at least 2 are positive, but sometimes only 1. Sometimes odd things happen, such as single nucleotide insertions or deletions, errors in the primer sequence itself, or part of the primer annealing with the wrong region of the template, but these results are rarely in all clones sequenced. If there are a lot of colonies on the control (25-50% of the experimental plates), you can sometimes get lucky. Consider longer DpnI digest or repeating.