Quantitative, multiplexed amplification with the Plexor qpcr Systems. Douglas R. Storts, Ph.D. Director R&D

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1 Quantitative, multiplexed amplification with the Plexor qpcr Systems Douglas R. Storts, Ph.D. Director R&D

2 Novel Base-Pairing IsoC & IsoG dntps Recognized by DNA Polymerase Do not base pair with ACGTU Licensed from EraGen Biosciences G isog C isoc Johnson, S.C., et al. (2004) Nucleic Acids Res. 32,

3 Use of IsoG and IsoC in Real-Time PCR Two primer method One standard primer One primer modified with iso-dc base and a fluorophore at 5 end Amplification master mix contains Standard dntps Dabcyl -labeled iso-dgtp Sherrill, C.B., et al. (2004) J. Amer. Chem. Soc. 126,

4 Dabcyl-iso-dGTP Contact Quenching Primers targeting different genes are labeled with iso-dc and different fluorophores Dabcyl-iso-dGTP incorporates opposite any iso-dc, resulting in contact quenching

5 Can Dabcyl Quench Red-Shifted Dyes? Dye FAM TET HEX ROX LC 640 Cy 5 % Quenching 62% 53% 71% 64% 48% 35% Emission Peak 518nm 536nm 554nm 606nm 640nm 667nm Table 1 in: Sherrill, C.B., et al. (2004) J. Amer. Chem. Soc. 126,

6 Typical Amplification Curves Gain of fluorescence Fluorescence Threshold Cycle

7 Plexor Amplification Curves Quenching of fluorescence Fluorescence Threshold Cycle

8 Plexor Method Same Data C t vs. concentration

9 Plexor Method Includes Melt Curves Confirmation of specificity

10 Multiplexing Applications Gene Expression Analysis

11 Large Dynamic Range Detection of various concentrations of a synthetic transcript in a constant background of 10ng human total RNA using one-step qrt-pcr Monoplex reaction Duplex reaction (also amplifying GAPDH) Dynamic Range: 10 1 to copies

12 Quantitation in Multiplex Experimental details 3 primer sets designed with Plexor Primer Design Software Biosearch Technologies dye sets All targets are human total RNA Plexor One-Step qrt-pcr System Thermal cycling performed on the Applied Biosystems 7500 Real Time PCR System

13 Consistent Quantitation in Multiplex C T Fibroblast Growth Factor Receptor 1 (FGFR1) - FAM Channel FGFR1 FGFR1 + GAPDH FGFR1 + MMP1 + GAPDH Monoplex R 2 = % Eff. Duplex R 2 = % Eff. Triplex R 2 = % Eff log pg total RNA template

14 Consistent Quantitation in Multiplex Matrix Metalloproteinase 1 (MMP1) - CalFluor Red 610 Channel C T MMP1 MMP1 + GAPDH MMP1 + FGFR1 + GAPDH Monoplex R 2 = % Eff. Duplex R 2 = % Eff. Triplex R 2 = % Eff log pg total RNA template

15 Consistent Quantitation in Multiplex Glyceraldehyde-3-phosphotransferase (GAPDH) - JOE Channel Monoplex R 2 = % Eff. Duplex R 2 = % Eff. Triplex R 2 = % Eff. C t GAPDH GAPDH + FGFR1 GAPDH + FGFR1 + MMP log pg total RNA template

16 4-Color Multiplexing Experimental Details 4 primer sets designed with Plexor Primer Design Software Biosearch Technologies dye sets All targets are human cdna Plexor Two-Step qrt-pcr System Thermal cycling performed on the Applied Biosystems 7500 Real Time PCR System

17 Quantitate High- & Low-Copy Together Quasar 670 GAPDH Cal Fluor Red 610 Integrin =0.1 cycles =0.4 cycles Red = Monoplex Blue = 4-plex Cal Fluor Orange 560 FGF receptor FAM Sulfotransferase AB 7500 =0.5 cycles =0.8 cycles

18 Plexor HY Assay Autosomal Titration series (3pg-50ng/µl) Data provided by J. Butler (NIST) Y Chromosome

19 Summary Two primer method allows easy multiplexing High correlation of C t values between monoplex and multiplex (less than 1 C t change) Accurate quantitation of lower copy messages in multiplex with high copy messages

20 Assay Design and Analysis Plexor Primer Design System and Analysis Software

21 Plexor Technology in Research Plexor Assay Design Plexor Reaction Plexor Data Analysis

22 Plexor Primer Design Website Free access (registration required) Select Instrument Input Target Sequence Choose Oligo Manufacturer Fluorescent Reporter Assigned Multiplex Reaction Design

23 Plexor Primer Design Web Site Sequence #1 Primer sets chosen for single product Powered by DNA Software Sequence #2 Sequence #3 Primer sets chosen for single product Primer sets chosen for single product Designed amplimers & primers checked for interactions Suggested Primers With BLAST links Sequence #4 Primer sets chosen for single product

24 BLAST Parser

25 Plexor Technology in Research Plexor Assay Design Plexor Reaction Plexor Data Analysis

26 Plexor Systems qpcr System Quantitation from genomic DNA, SNP genotyping For 2-step qrt-pcr methods with your cdna Two-step qrt-pcr System ImProm-II Reverse Transcriptase reagents for cdna synthesis Plexor Master Mix for qpcr from cdna template One-step qrt-pcr System Combines ImProm-II Reverse Transcriptase with Plexor Master Mix for qrt-pcr directly from RNA template

27 Plexor Reactions 25µl standard reaction 2X Plexor Master Mix contains: Enzyme (devoid of 5 exonuclease activity) High performance buffer Proprietary primer-dimer inhibitor datp, dctp, dgtp, dttp and Dabcyl-iso-dGTP For amplification of the DNA sequence of interest For incorporation opposite the iso-dc in the Plexor primers

28 Plexor Technology in Research Plexor Assay Design Plexor Reaction Plexor Data Analysis

29 Raw Data to Analyzed Data ABI Instruments Import Raw Data Roche Instruments Other Instruments

30 Supported Instruments Plexor reagents and Data Analysis Software for: ABI PRISM 7000 ABI PRISM 7700 AB 7300, 7500, 7900HT Corbett Rotor-Gene Roche LightCycler 1 & 2 Roche LightCycler 480 BioRad icycler (2 & 4 color) MJ Opticon Instruments Cepheid Instruments Stratagene Instruments et al.

31 Plexor Analysis Software Desktop

32 Summary Specificity from novel base-pairing Simple assay design Easy multiplex reactions Increased productivity Accurate quantitation Tools and support to employ Plexor technology freely available

33 Acknowledgements Research & Development Cheryl Bailey Gary Madsen Steve Ekenberg Nadine Nassif Katharine Hoffman Cynthia Sprecher Susan Frackman Douglas Storts Benjamin Krenke Software Thane Hafterson Jennifer McTaggart Lou Mezei Ethan Strauss Rick Smith Nucleic Acid Chemistry Amanda Glebs Julie Heger Dave Leland Kristina Pearson Jen Romanin Michael Ma Myra Schink Michael Ho Jim Prudent Mike Moser Scott Johnson Katie Zurbuchen

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