This method can help answer key questions in the field of DNA polymers fidelity and DNA repair such as proofreading methods and analysis and in defining the DNA repair patch. The main advantage of this technique is that it is very specific, simple, rapid, and easy to perform. Generally, individuals new to this method will struggle because of still they in DNA replication and the repair field may be not familiar with the mass spectrometry instrumentation and the data interpretation.
I think the most important is the visual demonstration is very critical as we can show how our commercially developed mass spectrometry for clinical applications such as mutation and deputation can be conveniently adapted for DNA proofreading and the repair study. Demonstrating the procedure will be Rong-Syuan and Kuei-Ching graduate students from my lab. Begin this procedure with primer and template preparation as described in the text protocol.
As an example, use a TG mismatch of substrate P21 with T28 for the proofreading. Dilute the P21 primer and the T28 template to 12.5 picomoles per microliter with water. Then, transfer 12 microliters of the diluted primer and 12 microliters of the diluted template to a 1.5 milliliter sterilized micro centrifuge tube.
After closing the tube tightly, incubate the tube for 30 minutes in a covered 65 degree Celsius water bath. Then, incubate for 30 minutes in a 37 degree Celsius water bath. And, finally, place the tube on ice to ensure a proper annealing.
To a 1.5 milliliter sterilized micro centrifuge tube, add eight microliters of primer and template mix, two microliters of 10x proofreading reaction buffer, four microliters of 4ddNTPs mix, and water up to 18 microliters. Flick the tube to mix. Dilute the DNA polymerase in ice cold 1x proofreading reaction buffer to the desired concentration.
Store the diluted enzyme on ice at all times. Pre-warm the micro centrifuge tube with the substrate mix to the desired reaction temperature. Then, transfer two microliters of the diluted DNA polymerase to the pre-warmed substrate mixture and flick the tube to mix its contents.
Centrifuge the tubes with enzyme and substrate for a few seconds at 3200 times gravity at ambient temperature to spin down the components of the reactions. Immediately transfer the reaction to a heating block or a water bath at the desired incubation temperature. To terminate the reaction, add an equal volume of buffered phenol and mix the reaction by vortexing for a few seconds.
Then, centrifuge the reaction in a micro-centrifuge at 3200 times gravity at ambient temperature for five minutes. Transfer the aqueous phase to a clean micro-centrifuge tube and add an equal volume of chloroform. After mixing it by vortexing for a few seconds, centrifuge the sample in a microcentrifuge at 3200 times gravity at ambient temperature for three minutes.
Transfer the aqueous phase to a clean micro-centrifuge tube. After incubating the reaction at 95 degrees Celsius for five minutes, place the tube on ice. Next, perform resin addition to eliminate salt contamination in a 384 well plate as detailed in the text protocol.
Set the sample plates in the nanoliter dispenser. Place the matrix chip and the prepared 384 well plate in the corresponding tray. Operate the nano-dispenser to spot the reaction products to the chip.
Push the run button on the touch screen of the nano-dispenser to start. Check the automated captured image of the sample spots containing saturation information on the screen to ensure the overall spotted volume on the chip is around five to 10 nanoliters. Repeat the sample spotting if the volume is insufficient.
Prepare a file in Excel format containing the anticipated signal information for importing. Create and define a new assay in the application program by right-clicking import assay group in designer format and select the Excel file. Establish the target assay plate via the customer project plate option tree on the left side of the screen by right-clicking the top of the tree and giving it a file name.
Select the 384 well plate type and press OK.A blank plate will appear. Select the appropriate assay on the left side of the screen. Assign the selected assay for each spotted sample position on the chip by highlighting the well and right-clicking to select add plex.
Next, prepare a working list of all the tests on the chip in Excel format with no header. Import the working list via the add new sample project option. Assign the test and the working list to each position of the P21T28 assay and choose by right-clicking.
Link the mass spectrometer to the chip using the application program. Select the default setting at the right side of the screen. Fill in the assay name and the chip ID at the corner of the chip.
Save the settings and start the MS control program. Press the in/out button and take out the scout plate. Place the spotted chip onto the scout plate and press the in/out button for the spotted chip to enter the mass spectrometer.
Click the acquire button of the application program to start the mass spectrometry and acquire the data. Open the program for the data analysis. Browse the tree of the database at the upper left corner and select the chip ID.Open the data file on the right side of the screen.
Click the spectrum icon to display the mass spectrum. To crop a specific range of mass over charge, right-click to select customization dialogue. In the new window, click on x-axis and set the desired upper and lower limit and press OK to show the specified range of the spectrum.
Export the spectrum for record keeping by right-clicking export. Select the JPEG file type, click on destination, select browse disc, type the file name, and then click on export. For data quantitation, use the cursor and click on the peak to show the peak height at the upper left hand corner.
In MALDI-TOF MS there is an inverse relationship between peak intensity in Oligonucleotide mass. Oligonucleotides from 17 to 24 nucleotides were subjected to an MS analysis. The relative signal intensities were calculated and could be used for quantification of the proofreading or repair assay.
Both template and primer signals could be found in the mass spectrum. Because of size differences, signals from templates and their non-specific partial degradation products were well separated from the mismatched primers and proofread products. Shown here is a proofreading of a three prime terminal TG.At five minutes, the corrected product was 23%versus 17%for the excision product.
This difference continued to increase to 69%versus 14%at 20 minutes. Note the high resolution of MS clearly separating the sub-straight and product signals with a mass overcharge difference of only 32. Also easily resolvable were two forms of excision products for a pen ultimate TG proofreading.
The one nucleotide excision intermediate and two nucleotide excision products. Proofreading of internal mismatches showed a clear trend in proofreading efficiency. As evidenced by a large proofread product speak, increased efficiency was observed when substraights had mismatches at the last, penultimate, third, and fourth nucleotides from the three prime end, as compared to mismatches at other positions.
Once mastered, this technique can be done in four hours if it is performed properly. Following this procedure, other applications like polymerous proofreading heapiter screening can be performed to discover and invent new drug for pharmaceutical research. This technique also paves the way for researchers in the field of DNA replication and repair to gain more insight into the medicine of the gnome and it's faithful replication for all living organisms.
After watching this video, you should have a good understanding of how to perform DNA proofreading and the repair assay using MADI-TOF mass spectrometry analysis. Don't forget that working with spheno-chloroform can be hazardous and the precautions, such as wearing personal protection gear, should always be taken while performing the procedure. The alternative protocol in the text could be considered as a safer substitute.
