Researchers often find probe and primer sequences for a specific qPCR assay in the literature, which they want to use for their own experiments. And why not? These sequences have already been vetted by other scientists and used successfully to generate publishable data.
Check published sequences against current sequence databases
However, before you order assays published in the literature, consider whether they were based on outdated sequence information. With the increasing amount of cataloged sequencing data, there has been a concomitant increase in the number of identified single nucleotide polymorphisms (SNPs) and updated transcript structure and annotation. While the frequency of SNP occurrence may make them unrealistic to avoid when choosing PCR primer and probe sequences (the human genome contains a SNP approximately once every 22 bases), it is important to take their position into consideration. See Considering SNPs when designing PCR and qPCR assays, for data on SNP frequency, and a discussion of the impact SNPs can have on PCR and qPCR assay results. The article also provides recommendations for managing SNP impact on your assay results.
Convert literature-derived probe sequences to more sensitive, double-quenched probes
Converting literature-derived probe sequences to double-quenched probes that contain an internal quencher has become popular over the past few years, due to the lower background fluorescence, increased signal, and reduced crosstalk double-quenched probes afford. This adaptation is easily done. IDT provides 2 types of internal quenchers, ZEN and TAO Internal Quenchers, that are compatible with a wide range of 5′ fluorescent dyes and 3′ quenchers (see Figure 1).
Evaluate your probe sequence
Adding ZEN or TAO Internal Quenchers into standard hydrolysis probe sequences with 5' fluorescent dyes and 3' quenchers is straightforward and will not appreciably affect probe Tm. However, note that probes from the literature containing MGB (or other Tm boosting modifiers) will have a reduced Tm when ordered without these modifications. Therefore, before ordering, it is a good idea to assess whether the published probe sequence has the ideal Tm to function optimally in your assays.
Use these steps to evaluate the published probe sequence before you order:
- Check the Tm of the probe sequence. If the probe Tm is not provided in the literature reference, use our free OligoAnalyzer Tool to calculate it. We recommend that the probe Tm be at least 4°C higher than primer Tm. Note that MGB (or other Tm boosting modified) probes from the literature will have a reduced Tm when ordered without these modifications.
- Determine whether you can modify your probe sequence. If the probe vs primer Tms do not meet the above criteria, you may need to either change the position of your assay or modify the probe sequence. Consider a predesigned assay for that exon location as the best primer probe combination is chosen (see the below sidebar, An alternative to published sequences). If the location of your probe cannot be moved, here are a few ways to modify your assay so that probe and primers will work optimally together during PCR.
- Change the length or position of your probe and/or primers so that primer and probe Tms meet the criteria in step 1 above.
- Increase the Tm of a short probe by adding bases onto the 5′ or 3′ end. Use the OligoAnalyzer Tool to assess Tm, and to rule out dimer formation between probe and primers, as well as secondary structure formation resulting from presence of the added bases.
- If you do not want to modify your probe sequence, another way to increase probe Tm is to replace 2–4 bases spaced throughout the sequence with locked nucleic acid bases. Locked nucleic acid bases are extremely stable and will raise probe Tm. Our Application Support Group can provide guidelines on where in the probe sequence to integrate locked nucleic acid bases. Contact them at firstname.lastname@example.org. Note that locked nucleic acid probes are not available as double-quenched probes; order them as single-quenched probes here.
Order the published probe sequence as a double-quenched probe
Now that you have confirmed your primer and probe sequences are up to date, and determined that the Tm of the probe sequence is optimal for use in your assay, convert a probe of your own design or one from the literature to one containing a ZEN or TAO Internal Quencher. Go to our qPCR probes design tool (Figure 2), and follow these steps to order the double-quenched version of the probe. To enter complete assays of both primer and probe sequences, use our qPCR assay design tool and follow these same steps):
Step 1. Provide a name for this sequence entry. (See the Step 1 blue arrow in Figure 2.)
Step 2. Select a synthesis scale. (See the Step 2 blue arrow in Figure 2.)
Step 3. Enter your sequence (e.g., copy and paste), without modifications. (See the Step 3 blue arrow in Figure 2.)
Step 4. Choose your 5' dye + 3' quencher combination from the dropdown list. (See the Step 4 blue arrow in Figure 2.) The dropdown list of modifications is shown in Figure 3. Note that with the 5′ dye choice, a compatible ZEN or TAO internal quencher will be automatically integrated into the appropriate position in your probe sequence.
Note that locked nucleic acid probes are not available as double-quenched probes; order them as single-quenched probes here.