METHODS AND DEVICES FOR MOLECULAR ASSOCIATION AND IMAGING

• US 20120108459A1
• Filed: 10/23/2011
• Published: 05/03/2012
• Est. Priority Date: 10/10/2007
• Status: Abandoned Application

• Current Assignee: BioTex Incorporated
• Original Assignee: BioTex Incorporated
• Inventors: Jackson, George, McNichols, Roger, Houssiere, Charles
• Application Number:
  US13/279,302
• Publication Number:
  US 20120108459A1
• Time in Patent Office: Days
• US Class Current: 506/9
• CPC Class Codes: B01L 2300/0636 Integrated biosensor, microarrays
• CPC Class Codes: B01L 2300/1822 using Peltier elements
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: B01L 7/52 with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples amplification or hybridisation processes per se C12Q1/68; controlling sequential reactions for synthesis B01J19/0046
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C40B 50/18 using a particular method of attachment to the solid support
• CPC Class Codes: C40B 60/14 for creating libraries

Abstract

The present invention is directed to devices and methods for molecular association, particularly to devices and methods for hybridization of nucleic acids utilizing temperature gradients and imaging thereof. In one aspect, a molecular hybridization system generally includes a substrate having a plurality of molecular probes attached thereto, the plurality of probes being generally present in multiple copies arranged in localized formations on the surface of the substrate. The molecular hybridization system further generally includes a chamber that encloses the plurality of molecular probes such that a fluid containing sample may be applied and kept in contact with the substrate having the probes thereon. The molecular hybridization system also includes a temperature affecting system that generally produces at least one desired temperature on the surface of the substrate and in the adjacent fluid within the chamber.

Claims

1. A method for diagnostic molecular association of a sample comprising:

disposing a fluid containing a sample for molecular association between a first and second substrate, said first substrate having an array of spots comprising biological material coupled to the substrate and said second substrate separated from the first substrate by a predetermined distance, said fluid occupying a chamber defined by said first and second substrates;

applying energy to said first substrate with a plurality of temperature affecting devices coupled to said first substrate, each of said temperature affecting devices sources providing at least one adjustable temperature to said first substrate and being disposed to create a temperature gradient profile along a surface of said first substrate; and

orienting said temperature gradient profile substantially along a gravitational field to generate Rayleigh-Benard instabilities;

whereby said temperature gradient profile enhances molecular association between molecules in said sample and a particular biological material coupled to said first substrate.

2. The method of claim 1, wherein said molecular association is a hybridization process.

3. The method of claim 1, wherein said array of spots are disposed to substantially optimize temperature-dependent molecular association with said sample based on the temperature gradient profile generated by said plurality of temperature affecting devices.

4. The method of claim 1, wherein the temperatures produced by said plurality of temperature affecting devices are adjusted by at least one controller to produce a desired temperature gradient profile.

5. The method of claim 4, wherein said at least one controller comprises at least one sensing device and a microprocessor.

6. The method of claim 1, further comprising adjusting the temperature of said first substrate with said plurality of temperature affecting devices coupled to said first substrate to create a temperature gradient profile along a surface of said first substrate;

and

monitoring the hybridization of said nucleic acid samples to the array of spots in real time to determine points for a melting curve;

whereby each spot is disposed at a position representative of an approximate temperature for simultaneously determining different temperature points on a melting curve.

7. A method for diagnostic molecular association of a sample comprising:

disposing a fluid containing a sample for molecular association between a first and second substrate, said first substrate having four corners and an array of spots comprising biological material coupled to the substrate and said second substrate separated from the first substrate by a predetermined distance, said fluid occupying a chamber defined by said first and second substrates;

applying energy to said first substrate with four temperature affecting devices coupled to said first substrate, each of said temperature affecting devices sources coupled to and providing at least one different adjustable temperature to said first substrate at a different corner to create a temperature gradient profile along a surface of said first substrate; and

orienting said temperature gradient profile substantially along a gravitational field to generate Rayleigh-Benard instabilities;

whereby said temperature gradient profile enhances molecular association between molecules in said sample and a particular biological material coupled to said first substrate.

8. The method of claim 7, wherein said molecular association is a hybridization process.

9. The method of claim 7, wherein said array of spots are disposed to substantially optimize temperature-dependent molecular association with said sample based on the temperature gradient profile generated by said temperature affecting devices.

10. The method of claim 7, wherein the temperatures produced by said temperature affecting devices are adjusted by at least one controller to produce a desired temperature gradient profile.

11. The method of claim 10, wherein said at least one controller comprises at least one sensing device and a microprocessor.

12. The method of claim 7, further comprising adjusting the temperature of said first substrate with said temperature affecting devices coupled to said first substrate to create a temperature gradient profile along a surface of said first substrate;

and

monitoring the hybridization of said nucleic acid samples to the array of spots in real time to determine points for a melting curve;

whereby each spot is disposed at a position representative of an approximate temperature for simultaneously determining different temperature points on a melting curve.

13. The method of claim 7, wherein said orienting comprises shifting said first substrate from a substantially horizontal orientation to a substantially vertical orientation.

14. The method of claim 7, wherein said temperature gradient profile is substantially continuous.

15. The method of claim 7, wherein said temperature gradient profile is substantially discontinuous.

16. A method for diagnostic molecular association of a sample comprising:

disposing a fluid containing a sample for molecular association between a first and second substrate, said first substrate having an array of spots comprising biological material coupled to the substrate and said second substrate separated from the first substrate by a predetermined distance, said fluid occupying a chamber defined by said first and second substrates; and

applying energy to said first substrate with a plurality of temperature affecting devices coupled to said first substrate, each of said temperature affecting devices sources providing at least one adjustable temperature to said first substrate and being disposed to create a temperature gradient profile along a surface of said first substrate;

whereby said temperature gradient profile enhances molecular association between molecules in said sample and a particular biological material coupled to said first substrate.

17. The method of claim 16 wherein said molecular association is a hybridization process.

18. The method of claim 16 wherein said array of spots are disposed to substantially optimize temperature-dependent molecular association with said sample based on the temperature gradient profile generated by said plurality of temperature affecting devices.

19. The method of claim 16 wherein said temperature gradient profile enhances mixing of said fluid in concert with a gravitational field.

20. The method of claim 16 wherein the temperatures produced by said plurality of temperature affecting devices are adjusted by at least one controller to produce a desired temperature gradient profile.