Hot start PCR
Hot start PCR is a modified form of conventional polymerase chain reaction that reduces the presence of undesired products and primer dimers due to non-specific DNA amplification at room temperatures. Because the results of PCR are so useful, many variations and modifications of the procedure were developed in order to achieve a higher yields, hot start PCR is one of them. Hot start PCR follows the same principles as the conventional PCR - in that it uses DNA polymerase to synthesise DNA from a single stranded template, however, it utilises additional heating and separation methods, such as inactivating or inhibiting the binding of Taq polymerase and late addition of Taq polymerase, to increase product yield as well as provide a higher specificity and sensitivity. Non-specific binding is minimized by completing the reaction mix after denaturation Some ways to complete reaction mixes at high temperatures involve modifications that block DNA polymerase activity in low temperatures, use of modified deoxyribonucleotide triphosphates, and the physical addition of one of the essential reagents after denaturation. The results of this procedure has many applications both medically and industrially. For example, applications of PCR including forensics, paternity testing, biodefence, cloning, mutation detection, genetic testing and DNA sequencing.
Through these additional methods, hot start PCR is able to decrease the amount of non-specific amplifications which naturally occur during lower temperatures – which remains a problem for conventional PCR. These modifications work overall to ensure that specific enzymes in solution will remain inactive or are inhibited until the optimal annealing temperature is reached.
Background
is a molecular biology technique used to amplify specific DNA segments by several orders of magnitude. The specific segments of DNA is amplified over three processes, denaturation, annealing and extension – where the DNA strands are separated by raising the temperature to the optimal from room temperature before primers bind and polymerase aligns nucleotides to the template strand. It uses DNA polymerase, which is slightly active at low temperatures. In conventional PCR, the reaction mix is completed at room temperature, and due to DNA polymerase activity, primers may form primer dimers or anneal to DNA non-specifically. During the PCR procedure, DNA polymerase will extend any piece of DNA with bound primers, generating target products but also nonspecific products which lower the yield. In hot start PCR, some of the reagents are kept separate until the mixture is heated to the specific annealing temperature. This reduces annealing time, which in turn reduces the likelihood of non-specific DNA extension and the influence of non-specific primer binding prior to denaturation.In conventional PCR, lower temperatures below the optimal annealing temperature results in off target modifications such as non-specific amplifications where primers will bind non-specifically to the nucleic acid. These non-specific primer complexes, which are in excess in the mixture, are the cause behind the synthesis of by-products such as primer dimer and mis-priming. Mis-priming greatly impedes and reduces the efficiency of PCR amplification through actively competing with the target sequences for amplification. Similarly, primer dimers form complexes which decreases the amount of copy number amplifications obtained. This can be controlled by implementing hot start PCR which allows primer extensions to be blocked until the optimal temperatures are met.
In hot start PCR, important reagents are prevented from reacting in the PCR mixture until the optimal temperatures are met through physical separation or chemical modifications. Hot start PCR can also occur when the Taq polymerase is inhibited/inactivated or its addition is delayed until optimal annealing temperatures, through deoxyribonucleotide triphosphate modifications or by modifying the primers through caging and secondary structure manipulation.
Hot start PCR is often a better approach opposed to traditional PCR in circumstances where there is a lack of DNA in the reaction mix, the DNA template is highly complex or if there are several pairs of oligonucleotide primers in the PCR.
Methods
Hot start PCR is a method which prevents DNA polymerase extension at lower temperature to prevent non-specific binding to minimise yield loss. Hot start PCR reduces the amount of non-specific binding through limiting reagents until the heating steps of PCR – limit the reaction early by limiting Taq DNA polymerase in a reaction. Non-specific binding often leads to primer dimers and mis-primed/false primed targets. These can be rectified through modified methods such as:Inactivation/Inhibition of Taq DNA polymerase
Enzyme linked antibodies:The enzyme linked antibodies inactivate the Taq DNA polymerase. The antibodies link and bind to the polymerase, preventing early DNA amplification which could occur at lower temperatures. Once the optimal annealing temperature is met, the antibodies will begin to degrade and dissociate, releasing the Taq DNA polymerase into the reaction and allowing the amplification process to start.
Wax beads:
A physical barrier is created between Taq DNA polymerase and the remainder of the PCR components by the wax beads which are temperature dependent. Once the temperature rises over 70 °C, during the denaturation step in the first cycle, the wax bead melts, allowing the Taq DNA polymerase to escape past the barrier and be released into the reaction – starting the amplification process. The wax layer then moves to the top of the reaction mixture during the amplification stage to later act as a vapour barrier.
Highly specific oligonucleotides:
Oligonucleotides are short polymers of nucleic acid which easily bind. Highly specific oligonucleotides, such as aptamers, bind to Taq DNA polymerase at lower temperatures making it inactive in the mixture. Only at higher temperatures will the oligonucleotides separate from the Taq allowing it to react.
These are the most effective methods for hot start PCR, the enzyme linked antibodies and highly specific oligonucleotides methods in particular are most suited during procedures which require a shorter inactivation time. However, other methods are known to be implemented such as:
Late addition of Taq DNA polymerase
Preheating:The PCR machine is heated in advance whilst the components are mixed over ice and then immediately placed into the PCR machine once it reaches optimum temperature. This would eliminate the warm-up process required, reduce non-specific annealing of the primers and ensures that any miss paired primers in the mixture are separated.
Freezing:
Freezing acts as a form of physical separation much like the wax beads. The reaction mixture containing primers, the template strand, water and deoxyribonucleotide triphosphate is frozen before Taq polymerase and the remaining PCR components are added on top of the frozen mixture. This acts to prevent non-specific binding.
Later addition of Taq:
The components of PCR in the reaction mix are prepared and heated without the addition of Taq. Taq is only later introduced into the mixture once the optimal temperature is reached. However, this method is the least reliable and may lead to a contamination of the components.
Another method is through deoxyribonucleotide triphosphate mediated hot start PCR which modifies the nucleotide bases through a protecting group.
Deoxyribonucleotide triphosphate (dNTP) modifications
Hot start dNTP can be chemically modified to include a heat sensitive protecting group at the 3 prime terminus. This modification will prevent the nucleotides from interacting with the Taq polymerase to bind to the template strand until after the optimal temperatures are reached therefore, the protecting group will be removed during the heat activation step. The hot start dNTP, dA, dT, dC and dG replace the natural nucleotides. Using all four of the modified nucleotides is recommended however, previous research shows that by replacing either one or two of the natural nucleotides with the modified dNTPs would be enough to ensure that non-specific amplification does not occur. Another chemical modification of nucleic acid is through the heat-reversible covalent modification which acts to impede the hybridisation of the primers to the template of interest. The guanosine amino group interact with glyoxal to form dG.Modified primers
Secondary structure:Certain secondary structure may impede the functions of the primers. For example, oligonucleotides with a hairpin structure cannot act efficiently as a primer. However, after heating the reaction mix to the annealing temperature the primer will undergo a conformation change allowing the primer to form a linear structure instead, which enables the primer to attach to the target segment and begin PCR.
Photochemically removable cages:
A caging group which is a protecting group that is photochemically removable, such as caged thymidine phosphoramidites, is incorporated into a oligonucleotide primer. This allows the function of the primer to be activated and deactivated through the use of UV irradiation. Therefore, primers can be activated after the annealing temperature is reached.