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

Patent metadata

Field	Value
Publication number	US-9983155-B2
Application number	US-201313840994-A
Country	US
Kind code	B2
Filing date	Mar 15, 2013
Priority date	Nov 16, 2000
Publication date	May 29, 2018
Grant date	May 29, 2018

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 system for performing a thermal denaturation analysis of a nucleic acid in a microfluidic device, the system comprising:
a microfluidic device having at least one microfluidic channel;
a loading device configured to introduce a fluid comprising the nucleic acid and amplification reagents into the microfluidic channel so that the fluid flows into the channel;
a heating system in communication with a temperature controller configured to cycle a fluid temperature in at least one portion of the microfluidic channel so that the nucleic acid undergoes amplification; and
the temperature controller configured to continuously increase a temperature of the fluid containing the amplified nucleic acid in at least one portion of the channel to cause denaturation of the nucleic acid after the amplification is completed;
a detector configured to measure a detectable property emanating from the fluid containing the amplified nucleic acid in the at least one portion of the microfluidic channel as a function of a continuously increasing temperature, the detectable property being indicative of the extent of denaturation of the nucleic acid, the detectable property decreasing as a nucleic acid molecule denatures in real time, wherein the amplification and the measurement of the detectable property are performed in the same channel, wherein the fluid flow during the amplification is subject to the same flow control as the fluid flow during the thermal melt denaturation; and
a controller configured to generate a thermal property curve representing the measured detectable property as a function of the continuously increasing temperature and determine a nucleic acid melting temperature based on the thermal property curve.

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

3. The system of claim 1 , wherein the loading device comprises a pipettor extending from the microfluidic device and is in communication with the channel.

4. The system of claim 1 , wherein the fluid control is limited to controlling a pressure differential between two locations at the microfluidic channel, wherein the amplification portion of the channel and the denaturation portion of the channel are positioned between the two locations along the channel.

5. The system of claim 1 , wherein the fluid is stopped in the at least one portion of the channel to perform the amplification followed by the nucleic acid denaturation analysis including measuring the detectable property as a function of a continuously increasing temperature.

6. The system of claim 5 , wherein the at least one portion of the channel containing the stopped fluid is in communication with the heating system varying the temperature in the at least one portion of the channel to perform the amplification and the denaturation analysis.

7. The system of claim 5 , wherein the temperature of the fluid is continuously increased at a rate in the range of 0.1° C./second to 1° C./second.

8. The system of claim 5 , 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.

9. The system of claim 5 , wherein the temperature of the fluid is continuously increased at a rate in the range of 1° C./second to 10° C./second.

10. The system of claim 1 , wherein the fluid continuously flows through the at least one portion of the channel and the amplification and the denaturation analysis are performed in the continuously flowing fluid.

11. The system of claim 10 , wherein the at least one portion of the channel containing the continuously flowing fluid is in communication with the heating system varying the temperature in the at least one portion of the channel to perform the amplification and the denaturation analysis including measuring the detectable property as a function of a continuously increasing temperature.

12. The system of claim 1 , wherein the cycling of the temperature of the at least one portion of the microfluidic channel comprises varying an electric current used to joule heat the at least one portion.

13. The system of claim 1 , wherein the cycling of the temperature of the at least one portion of the microfluidic channel comprises varying the temperature of the at least one portion using a non-joule heating system.

14. The system of claim 13 , wherein the non-joule heating system 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.

15. The system of claim 13 , wherein the non-joule heating system 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.

16. The system of claim 15 , wherein the resistive heating elements are fabricated onto a surface of the microfluidic device.

17. The system of claim 1 , wherein the amplification is performed by using a technique selected from a group consisting of: PCR and LCR.

18. The system of claim 1 , wherein the amplification reagents include primers, a thermostable polymerase, and nucleotides.

19. The system of claim 1 , wherein the detectable property comprises fluorescence.

20. The system of claim 19 , wherein the fluorescence is generated by FRET or a molecular beacon.

21. The system of claim 19 , 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.

22. The system of claim 21 , wherein the fluorescent dye is selected from the group consisting of: an intercalating dye, ethidium bromide, a minor groove binding dye, and a SYBR green dye.

23. The system of claim 1 , wherein the detectable property is selected form the group consisting of: fluorescence polarization, UV absorbance.

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

25. The system of claim 1 , wherein the system further comprises:
a fluid comprising a molecule of a known melt temperature (Tm), the fluid flowing through the channel, wherein a physical parameter that correlates with the temperature within the channel is being varied,
a detector configured to measure a value of the detectable property of the molecule as a function of the parameter, wherein the thermal property curve for the molecule is generated; and
a processor configured to determine the values of the detectable property and the parameter at the point in the thermal property curve that corresponds to the Tm of the molecule and derive the fluid temperature in the channel of microfluidic device based upon the determined values of the detectable property and the parameter.

26. The system of claim 25 , wherein the molecule of known Tm is selected from the group consisting of: a nucleic acid with a known sequence, biotin, biotin-4-fluorescein, fluorescein biotin, avidin, streptavidin, and neutravidin.

27. The system of claim 25 , wherein the physical parameter is selected from the group consisting of: the temperature of a thermal block in thermal contact with the channel, the current applied to the fluid in order to

Assignees

• Canon Us Life Sciences Inc
• Caliper Life Sciences Inc

Inventors

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

Classifications

• B01L2200/10

  Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept · CPC title

• G01N21/6428

  Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" (in vivo A61B5/00; immunoassay G01N33/53) · CPC title

• B01L2300/0627

  Sensor or part of a sensor is integrated · CPC title

• B01L2400/0487

  fluid pressure, pneumatics · CPC title

• B01L2300/0816

  Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title