Sign in

What PCR is

Polymerase Chain Reaction (PCR) is a widely used molecular biology technique for amplifying DNA segments. However, PCR can be challenging when the DNA template has a high GC content. GC-rich DNA sequences can form secondary structures that hinder the binding of primers and the activity of the DNA polymerase. In this blog post, we will explore some tips and tricks for amplifying DNA segments with high GC content by PCR.

Optimize the Annealing Temperature: The annealing temperature is a critical parameter for PCR amplification. In general, higher annealing temperatures are required for GC-rich templates because of the high melting temperature of the DNA duplex. A good starting point is to use an annealing temperature that is 5-10°C higher than the melting temperature (Tm) of the primers.

Use Long Primers: Longer primers can improve the specificity and efficiency of PCR amplification. In particular, primers with a length of 25-30 nucleotides are recommended for GC-rich templates. Longer primers can also increase the annealing temperature, which can help overcome the secondary structures of the template.

Add DMSO or Betaine to the Reaction: DMSO and betaine are commonly used additives to PCR reactions to improve the amplification of GC-rich templates. DMSO can denature secondary structures of DNA, while betaine stabilizes the DNA duplex and prevents the formation of secondary structures.

Use a Two-Step PCR Protocol: A two-step PCR protocol can also improve the amplification of GC-rich templates. In this protocol, the annealing and extension steps are combined to reduce the time that the template spends in the partially annealed state. The two-step protocol also helps to minimize the formation of secondary structures during the PCR reaction.

Use a Touchdown PCR Protocol: A touchdown PCR protocol is a step-down annealing temperature PCR that can increase the specificity of PCR amplification of GC-rich templates. In this protocol, the annealing temperature is gradually reduced over several cycles until it reaches the Tm of the primers. This approach increases the specificity of the PCR reaction by allowing the primers to bind specifically to the template DNA.

Include a Denaturation Step: A denaturation step can be included in the PCR protocol to reduce the secondary structure of the template DNA. The denaturation step can be performed by heating the DNA to 95°C for 5-10 minutes before starting the PCR reaction.

Choice of robust polymerase: SynPhusion DNA polymerase is especially suitable for the amplification of DNA regions with a high GC content, even in places where other DNA polymerases, such as Taq or Pfu polymerases, are not capable of amplification.

In conclusion, PCR amplification of GC-rich DNA segments can be a challenging task. However, by choosing the right DNA polymerase, optimizing the annealing temperature, using long primers, adding DMSO or betaine to the reaction, using a two-step or touchdown PCR protocol or including a denaturation step, high-quality PCR products can be obtained for downstream applications such as cloning and sequencing library preparation. With these tips and tricks, hard PCR amplification of GC-rich DNA templates can be achieved with high efficiency and specificity.

Tags :
Share This :