Melting curve analysis

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Melting curve analysis is an assessment of the dissociation characteristics of double-stranded DNA during heating. As the temperature is raised, the double strand begins to dissociate leading to a rise in the absorbance intensity, hyperchromicity. The temperature at which 50% of DNA is denatured is known as the melting temperature.

The information gathered can be used to infer the presence and identity of single-nucleotide polymorphisms (SNP). This is because G-C base pairing have 3 hydrogen bonds between them while A-T base pairs have only 2. DNA with a higher G-C content, whether because of its source (G-C contents: E. coli 0.50, M. luteus 0.72, poly d(AT) 0.00) or, as previously mentioned, because of SNPs, will have a higher melting temperature than DNA with a higher A-T content.

The information also gives vital clues to a molecule's mode of interaction with DNA. Molecules such as intercalators slot in between base pairs and interact through pi stacking. This has a stabilizing effect on DNA's structure which leads to a raise in its melting temperature. Likewise, increasing salt concentrations helps diffuse negative repulsions between the phosphates in the DNA's backbone. This also leads to a rise in the DNA's melting temperature. Conversely, pH can have a negative effect on DNA's stability which may lead to a lowering of its melting temperature.


Graphs to show the relation between fluorescence and temperature for labeled probe designed for a Wt sequence, homozygous Wt, heterozygous and homozygous mutant situations

The energy required to break the base-base hydrogen bonding between two strands of DNA is dependent on their length, GC content and their complementarity. By heating a reaction-mixture that contains double-stranded DNA sequences and measuring dissociation against temperature, these attributes can be inferred.

Originally, strand dissociation was observed using UV absorbance measurements,[1] but techniques based on fluorescence measurements[2] are now the most common approach.

The temperature-dependent dissociation between two DNA-strands can be measured using a DNA-intercalating fluorophore such as SYBR green, EvaGreen or fluorophore-labelled DNA probes. In the case of SYBR green (which fluoresces 1000-fold more intensely while intercalated in the minor groove of two strands of DNA), the dissociation of the DNA during heating is measurable by the large reduction in fluorescence that results.[3] Alternatively, juxtapositioned probes (one featuring a fluorophore and the other, a suitable quencher) can be used to determine the complementarity of the probe to the target sequence.[3]

The graph of the negative first derivative of the melting-curve may make it easier to pin-point the temperature of dissociation (defined as 50% dissociation), by virtue of the peaks thus formed.

SYBR Green enabled product differentiation in the LightCycler in 1997.[4] Hybridization probes (or FRET probes) were also demonstrated to provide very specific melting curves from the single-stranded (ss) probe-to-amplicon hybrid. Idaho Technology and Roche have done much to popularize this use on the LightCycler instrument.


Since the late 1990s product analysis via SYBR Green, other double-strand specific dyes, or probe-based melting curve analysis has become nearly ubiquitous. The probe-based technique is sensitive enough to detect single-nucleotide polymorphisms (SNP) and can distinguish between homozygous wildtype, heterozygous and homozygous mutant alleles by virtue of the dissociation patterns produced. Without probes, amplicon melting (melting and analysis of the entire PCR product) was not generally successful at finding single base variants through melting profiles. With higher resolution instruments and advanced dyes, amplicon melting analysis of one base variants is now possible with several commercially available instruments. For example: Applied Biosystems 7500 Fast System and the 7900HT Fast Real-Time PCR System, Idaho Technology's LightScanner (the first plate-based high resolution melting device), Qiagen's Rotor-Gene instruments, and Roche's LightCycler 480 instruments.

Many research and clinical examples[5] exist in the literature that show the use of melting curve analysis to obviate or complement sequencing efforts, and thus reduce costs.

While most quantitative PCR machines have the option of melting curve generation and analysis, the level of analysis and software support varies. High Resolution Melt (known as either Hi-Res Melting, or HRM) is the advancement of this general technology and has begun to offer higher sensitivity for SNP detection within an entire dye-stained amplicon. It is less expensive and simpler in design to develop probeless melting curve systems. However, for genotyping applications, where large volumes of samples must be processed, the cost of development may be less important than the total throughput and ease of interpretation, thus favoring probe-based genotyping methods.

See also[edit]


  1. ^ Ansevin, A.T.; Vizard, D.L.; Brown, B.W.; McConathy, J. (1976), "High-resolution thermal denaturation of DNA. I. Theoretical and practical considerations for the resolution of thermal subtransitions", Biopolymers, 15 (1): 153–74, doi:10.1002/bip.1976.360150111, PMID 1244898
  2. ^ Ririe, K.M.; Rasmussen, R.P.; Wittwer, C.T. (1997), "Product differentiation by analysis of DNA melting curves during the polymerase chain reaction", Anal. Biochem., 245 (2): 154–60, doi:10.1006/abio.1996.9916, PMID 9056205
  3. ^ a b Hou, Shaw (2010). Biocatalysis and Biomolecular Engineering. John Wiley & Sons. pp. 314–317.
  4. ^ Ririe, 1997
  5. ^ Lay MJ, Wittwer CT. (1997) Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR. Clin Chem. 1997 Dec;43(12):2262-7
  6. ^ Wienken CJ, Baaske P, Duhr S, Braun D (2011), "Thermophoretic melting curves quantify the conformation and stability of RNA and DNA", Nucleic Acids Research, 39 (8): e52–e52, doi:10.1093/nar/gkr035, PMC 3082908, PMID 21297115.

External links[edit]