Oligonucleotide arrays comprising background probes

• US 20060057587A1
• Filed: 09/13/2004
• Published: 03/16/2006
• Est. Priority Date: 09/13/2004
• Status: Abandoned Application

• Current Assignee: Agilent Technologies, Inc.
• Original Assignee: Agilent Technologies, Inc.
• Inventors: Leproust, Eric M., Vacha, Scott J.
• Application Number:
  US10/939,650
• Publication Number:
  US 20060057587A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2545/101 with an internal standard/control

Abstract

The invention relates to chemical arrays comprising a plurality of features comprising biopolymers at known locations on the substrate, wherein at least one feature comprises specific hybridization probes designed or selected to bind to specific target sequences and background probes for evaluating non-specific binding of target. Methods, systems, and kits for making and using the arrays are also described.

Claims

1. A method for making a chemical array comprising:

arraying a plurality of biopolymers on a substrate, thereby forming a plurality of features comprising biopolymers at known locations on the substrate,

wherein at least one feature comprises specific hybridization probes designed or selected to specifically bind to target sequences and background probes for evaluating non-specific binding of target.

2. The method of claim 1, wherein biopolymers forming features are synthesized in situ on the substrate.

3. The method of claim 1, wherein the biopolymers comprise nucleic acids.

4. The method of claim 1, wherein the background probes are located at the perimeter of the feature.

5. The method of claim 4, wherein the specific hybridization probes are located at the center of the feature.

6. The method of claim 1, wherein the specific hybridization probes are on average about 60 base pairs or greater.

7. The method of claim 1, wherein the specific hybridization probes are on average less than about 60 base pairs.

8. The method of claim 1, wherein the background probes comprise fewer base pairs than the specific hybridization probes.

9. The method of claim 1, wherein the background probes comprise at least about 5 base pairs.

10. The method of claim 1, wherein the background probes comprise at least about 10 base pairs.

11. The method of claim 1, wherein specific hybridization probes are formed by iteratively depositing nucleotide monomers at a selected location within a feature to form a biopolymer.

12. The method of claim 1, wherein specific hybridization probes are formed by iteratively depositing nucleotide monomers at a location within a feature to form a biopolymer of n base pairs, while limiting biopolymer formation at another location within the feature to form a biopolymer of fewer than n base pairs.

13. The method of claim 12, wherein nucleotide monomers are deposited in droplets of decreasing volume at the feature.

14. The method of claim 12, wherein nucleotide monomers are deposited in droplets by a droplet dispenser and either or both the droplet dispenser or substrate is moved so that the droplet falls on a location of the feature to comprise specific hybridization probes and does not fall on a location of the feature to comprise background probes.

15. The method of claim 12, wherein the background probes are selectively blocked while nucleotide monomers are deposited.

16. The method of claim 12, wherein, specific hybridization probes are selectively activated while nucleotide monomers are deposited.

17. A chemical array formed by the method of claim 1.

27. A system for performing a method according to claim 1, comprising:

a substrate holder for retaining a substrate;

a head comprising a drop dispenser comprising an opening facing a retained substrate for depositing agents for biopolymer synthesis on the retained substrate;

a transport system for moving the head and/or drop dispenser relative to the substrate; and

a processor for controlling the ejection of drops from the drop dispenser onto the substrate according to a predetermined pattern during movement of the head and/or drop dispenser relative to the substrate, thereby forming a pattern of features comprising biopolymers on the substrate,

wherein the pattern includes formation of at least one feature comprising background probes and specific hybridization probes.

28. The system of claim 27, wherein the processor provides instructions for changing the volume of a drop ejected from the drop dispenser after a selected number of passes of the drop dispenser over a location on the substrate.

29. The system of claim 27, wherein the processor offsets the position of the drop dispenser relative to a location receiving previously deposited drops.

30. A computer program product comprising instructions for forming a pattern of features on an array using a system according to claim 27, at least one feature comprising specific hybridization probes designed or selected to specifically bind to target sequences and background probes for evaluating non-specific binding of target.

33. A method for ordering a chemical array comprising at least one feature comprising background probes and specific hybridization probes, comprising providing instructions to the processor of the system of claim 27, specifying the predetermined pattern.

34. The method of claim 33, wherein the instructions comprise instructions relating to the sequence of the background probes and/or the specific hybridization probes.

35. The method of claim 33, wherein the instructions comprise instructions relating to the location of features on the substrate.

18. A chemical array comprising a plurality of features, wherein each feature comprises a plurality of specific hybridization probes and background probes, and wherein the background probe sequences comprise a subsequence of the specific hybridization probes and background probes within at least two features are identical.

19. The array of claim 18, wherein each feature comprises substantially identical background probes.

20. A substrate comprising a plurality of chemical arrays, wherein one of the plurality of arrays is an array according to claim 18.

22. The method of claim 19, wherein the target is labeled with a fluorescent label and the detecting step comprises determining intensity of fluorescence at the feature.

23. The method of claim 19, wherein each feature comprises background probes comprising less than about 20 base pairs in length.

24. The method of claim 19, wherein the specific hybridization probes are about 60 base pairs in length.

25. The method of claim 19, wherein background probes are about 10 base pairs in length.

26. The method of claim 19, wherein the specific hybridization probes are about 25 base pairs in length.

21. A method for detecting specific binding of a target molecule in a sample to a probe comprising:

providing an array comprising a plurality of biopolymer features arrayed at known locations on a substrate, wherein at least one feature comprises a plurality of specific hybridization probes and a plurality of background probes;

detecting binding of target to a feature and determining an amount of binding at the feature;

determining an amount of binding of target to background probes in the feature to determine an amount of non-specific binding.

31. A method for evaluating non-specific background signal at a feature on a chemical array which comprises background probes and specific hybridization probes, comprising:

positioning a template within an area of an array or an image of an array that is predicted to have a feature deposited or written thereon, wherein the template conforms in dimensions to an area of a feature comprising background probes, and excludes an area of the feature comprising specific hybridization probes; and

extracting feature information within the template area.

32. A method comprising:

receiving data for a feature on a chemical array comprising both specific hybridization probes designed or selected to specifically bind to target sequences and background probes for evaluating non-specific binding of target; and

detecting an amount of specific hybridization to the target sequences.