SYTO dyes and EvaGreen outperform SYBR Green in real-time PCR

被引:85
作者
Eischeid A.C. [1 ]
机构
[1] Division of Bioanalytical Chemistry, Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, College Park, MD 20740
关键词
Reaction Efficiency; Reaction Inhibition; Linear Standard Curve; High Resolution Melt Curve Analysis; High Reaction Efficiency;
D O I
10.1186/1756-0500-4-263
中图分类号
学科分类号
摘要
Background: Real-time PCR can be carried out using either probes or DNA dyes. SYBR Green has been used the most, but it suffers from several drawbacks. Numerous other DNA dyes are commercially available, but with limited structural information. Dye behavior in real time PCR is difficult to predict, so empirical data are needed. In the work described here, a panel of 23 different DNA dyes - including green, orange, and red SYTO dyes, EvaGreen, and SYBR Green - were evaluated with respect to their performance in real time PCR. Findings. Data were analyzed for reaction inhibition, effects on amplicon melting temperature, fluorescent signal strength, and reaction efficiency. This is the first report of reaction efficiency using alternatives to SYBR Green. Results indicated substantial variation in performance even within the SYTO dye family. EvaGreen and the SYTO dyes 13, 16, 80, and 82 performed better than SYBR Green in general, and high reaction efficiencies can be achieved using these dyes. Conclusions: Empirical data were generated for 23 DNA dyes. This paper confirms and extends previous findings that among commercially available DNA dyes, EvaGreen and certain SYTO dyes are the most desirable alternatives to the commonly used SYBR Green in real-time PCR. © 2011 Eischeid et al; licensee BioMed Central Ltd.
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  • [1] Higuchi R., Fockler C., Dollinger G., Watson R., Kinetic PCR analysis: Real-time monitoring of DNA amplification reactions, Bio/Technology, 11, 9, pp. 1026-1030, (1993)
  • [2] Wilhelm J., Pingoud A., Real-Time Polymerase Chain Reaction, ChemBioChem, 4, 11, pp. 1120-1128, (2003)
  • [3] Gasparic M.B., Tengs T., La Paz J.L., Holst-Jensen A., Pla M., Esteve T., Zel J., Gruden K., Comparison of nine different real-time PCR detection chemistries for qualitative and quantitative applications in GMO detection, Anal Bioanal Chem, 396, pp. 2023-2029, (2010)
  • [4] Ririe K.M., Rasmussen R.P., Wittwer C.T., Product differentiation by analysis of DNA melting curves during the polymerase chain reaction, Analytical Biochemistry, 245, 2, pp. 154-160, (1997)
  • [5] Anderson T.P., Werno A.M., Beynon K.A., Murdoch D.R., Failure to genotype herpes simplex virus by real-time PCR assay and melting curve analysis due to sequence variation within probe binding sites, Journal of Clinical Microbiology, 41, 5, pp. 2135-2137, (2003)
  • [6] Papin J.F., Vahrson W., Dittmer D.P., SYBR Green-Based Real-Time Quantitative PCR Assay for Detection of West Nile Virus Circumvents False-Negative Results Due to Strain Variability, Journal of Clinical Microbiology, 42, 4, pp. 1511-1518, (2004)
  • [7] Gudnason H., Dufva M., Bang D.D., Wolff A., Comparison of multiple DNA dyes for real-time PCR: Effects of dye concentration and sequence composition on DNA amplification and melting temperature, Nucleic Acids Research, 35, 19, (2007)
  • [8] Giglio S., Monis P.T., Saint C.P., Demonstration of preferential binding of SYBR Green i to specific DNA fragments in real-time multiplex PCR, Nucleic Acids Res, 31, 22, (2003)
  • [9] Varga A., James D., Real-time RT-PCR and SYBR Green I melting curve analysis for the identification of Plum pox virus strains C, EA, and W: Effect of amplicon size, melt rate, and dye translocation, Journal of Virological Methods, 132, 1-2, pp. 146-153, (2006)
  • [10] Wittwer C.T., Reed G.H., Gundry C.N., Vandersteen J.G., Pryor R.J., High-resolution genotyping by amplicon melting analysis using LCGreen, Clinical Chemistry, 49, 6, pp. 853-860, (2003)