Method and apparatus for generating thermal melting curves in a microfluidic device

Patent metadata

Field	Value
Publication number	US-9376718-B2
Application number	US-201213444502-A
Country	US
Kind code	B2
Filing date	Apr 11, 2012
Priority date	Nov 16, 2000
Publication date	Jun 28, 2016
Grant date	Jun 28, 2016

Abstract

The present invention provides novel methods and devices that employ microfluidic technology to generate molecular melt curves. In particular, the devices and methods in accordance with the invention are useful in providing for the analysis of PCR amplification products.

First claim

The invention claimed is:

1. A method of performing thermal melt analysis of a nucleic acid in a microfluidic device, the method comprising:
providing a microfluidic device having at least one microfluidic channel,
introducing fluid comprising the nucleic acid and amplification reagents into the microfluidic channel so that the fluid continuously flows through the channel,
cycling the temperature in at least one portion of the microfluidic channel so that the nucleic acid undergoes amplification, wherein the cycling of the temperature comprises varying the temperature of the at least one portion using a non-joule heating method,
after the amplification is completed, subjecting the fluid to a continuously increasing series of temperatures in the same microfluidic channel, wherein the series of temperatures includes a temperature high enough to cause denaturation of the nucleic acid, and
measuring a detectable property emanating from the fluid in the same microfluidic channel while subjecting the fluid to the continuously increasing series of temperatures, wherein the detectable property is indicative of the extent of denaturation of the nucleic acid.

2. The method of claim 1 , wherein the nucleic acid is DNA.

3. The method of claim 1 , wherein the step of introducing fluid into at least one of the microfluidic channels comprises introducing fluid through a pipettor extending from the microfluidic device.

4. The method of claim 1 , wherein the fluid is induced to flow into the channel by means of a pressure differential applied to the microfluidic channel.

5. The method of claim 1 , wherein the at least one portion of the microfluidic channel comprises the entire channel.

6. The method of claim 1 , wherein the step of cycling the temperature comprises cycling the temperature of at least one portion of the microfluidic channel, whereby the number of temperature cycles the fluid is subjected to is determined by the amount of time the fluid remains in that portion of the microfluidic channel.

7. The method of claim 1 , wherein the non-joule heating method comprises placing the at least one portion of the microfluidic channel in thermal contact with a thermal block, wherein the temperature is cycled by varying the temperature of the thermal block.

8. The method of claim 1 , wherein the non-joule heating method comprises passing an electric current through resistive heating elements in thermal contact with the at least one portion of the microfluidic channel, wherein the temperature is cycled by varying the current passing through the resistive heating elements.

9. The method of claim 8 , wherein the resistive heating elements are fabricated onto a surface of the microfluidic device.

10. The method of claim 8 , wherein the non-joule heating method further comprises placing an energy sink in thermal contact with the at least one channel.

11. The method of claim 1 , wherein the amplification comprises the use of PCR.

12. The method of claim 11 , wherein the amplification reagents comprise primers, a thermostable polymerase, and nucleotides.

13. The method of claim 1 , wherein the amplification comprises the use of LCR.

14. The method of claim 1 , wherein the step of subjecting the fluid to a series of temperatures comprises varying the temperature of stationary fluid contained within the at least one portion.

15. The method of claim 14 , wherein varying the temperature of the fluid comprises continuously increasing the temperature of the fluid.

16. The method of claim 15 , wherein the temperature of the fluid is continuously increased at a rate in the range of 0.1° C/second to 1° C/second.

17. The method of claim 15 , wherein the temperature of the fluid is continuously increased at a rate in the range of 0.01° C/second to 0.1° C/second.

18. The method of claim 15 , wherein the temperature of the fluid is continuously increased at a rate in the range of 1° C/second to 10° C/second.

19. The method of claim 15 , wherein the temperature of the fluid is continuously increased using non-joule heating.

20. The method of claim 19 , wherein the non-joule heating comprises heating the at least one portion of the microfluidic channel using a thermal block in thermal contact with the at least one portion.

21. The method of claim 1 , wherein the detectable property comprises fluorescence.

22. The method of claim 21 , wherein the fluorescence is generated by FRET or a molecular beacon.

23. The method of claim 22 , wherein the fluorescence is generated by a fluorescent dye, and wherein the amount of fluorescence generated by the fluorescent dye is indicative of the extent of thermal denaturation of the nucleic acid.

24. The method of claim 23 , wherein the fluorescent dye is an intercalating dye.

25. The method of claim 24 , wherein the fluorescent dye is ethidium bromide.

26. The method of claim 23 , wherein the fluorescent dye is a minor groove binding dye.

27. The method of claim 26 , wherein the fluorescent dye is a SYBR green dye.

28. The method of claim 1 , wherein the detectable property is fluorescence polarization.

29. The method of claim 1 , wherein the detectable property is UV absorbance.

30. The method of claim 1 , wherein the detectable property is selected from the group of heat capacity, electrical resistance, and dielectric properties.

31. The method of claim 1 , wherein the step of measuring the detectable property occurs concurrently in each microfluidic channel that received fluid during the introducing fluid step.

Assignees

• Sundberg Steven A
• Knapp Michael R
• Knight Ivor T
• Boles Deborah J
• Rulison Aaron J
• Dong Wesley B
• Donlon Edward P
• Moti Robert J
• Fabans Andrew G
• Boronkay Allen R
• Slater Michael
• Caliper Life Sciences Inc
• Canon Us Life Sciences Inc

Inventors

• Sundberg Steven A
• Knapp Michael R
• Knight Ivor T
• Boles Deborah J
• Rulison Aaron J
• Dong Wesley B
• Donlon Edward P
• Moti Robert J
• Fabans Andrew G
• Boronkay Allen R
• Slater Michael

Classifications

• C12Q1/68

  involving nucleic acids · CPC title

• B01L2400/0415

  electrical forces, e.g. electrokinetic · CPC title

• C12Q1/686 Primary

  Polymerase chain reaction [PCR] · CPC title

• B01L2400/0487

  fluid pressure, pneumatics · CPC title

• Y10T436/143333

  Saccharide [e.g., DNA, etc.] · CPC title