Controlled alignment of nano-barcodes encoding specific information for scanning probe microscopy (SPM) reading

• US 7,476,786 B2
• Filed: 09/19/2003
• Issued: 01/13/2009
• Est. Priority Date: 09/20/2002
• Status: Expired due to Fees

• Current Assignee: Intel Corporation
• Original Assignee: Intel Corporation
• Inventors: Yamakawa, Mineo, Su, Xing, Chan, Selena
• Primary Examiner(s): LU, FRANK WEI MIN
• Application Number:
  US10/667,004
• Publication Number:
  US 20040126820A1
• Time in Patent Office: 1,943 Days
• Field of Search: 435/6, 435/7.1, 435/91.1, 435/183, 435/283.1, 435/287.1, 435/287.2, 436/94, 436/501, 536/23.1, 536/24.3, 536/24.33, 536/25.3, 530/300, 530/350, 977/702, 977/704, 977/705, 977/728, 977/729, 977/734, 977/742, 977/773, 977/774
• US Class Current: 435/6.14
• CPC Class Codes: B82Y 10/00 Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
• CPC Class Codes: B82Y 30/00 Nanotechnology for materials or surface science, e.g. nanocomposites
• CPC Class Codes: B82Y 5/00 Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 2563/185 Nucleic acid dedicated to use as a hidden marker/bar code, e.g. inclusion of nucleic acids to mark art objects or animals
• CPC Class Codes: C12Q 2565/601 being a microscope, e.g. atomic force microscopy [AFM]
• CPC Class Codes: Y10S 977/702 having biological material component
• CPC Class Codes: Y10S 977/704 Nucleic acids, e.g. DNA or RNA
• CPC Class Codes: Y10S 977/705 Protein or peptide
• CPC Class Codes: Y10S 977/728 Nucleic acids, e.g. DNA or RNA
• CPC Class Codes: Y10S 977/729 From protein or unit thereof, e.g. enzyme or carboxyl group
• CPC Class Codes: Y10S 977/734 Fullerenes, i.e. graphene-based structures, such as nanohorns, nanococoons, nanoscrolls or fullerene-like structures, e.g. WS2 or MoS2 chalcogenide nanotubes, planar C3N4, etc.
• CPC Class Codes: Y10S 977/742 Carbon nanotubes, CNTs
• CPC Class Codes: Y10S 977/773 Nanoparticle, i.e. structure having three dimensions of 100 nm or less
• CPC Class Codes: Y10S 977/774 Exhibiting three-dimensional carrier confinement, e.g. quantum dots
• CPC Class Codes: Y10S 977/924 using nanostructure as support of dna analysis

Abstract

The methods, apparatus and compositions disclosed herein concern the detection, identification and/or sequencing of biomolecules, such as nucleic acids or proteins. In certain embodiments of the invention, coded probes comprising a probe molecule attached to one or more nano-barcodes may be allowed to bind to one or more target molecules. After binding and separation from unbound coded probes, the bound coded probes may be aligned on a surface and analyzed by scanning probe microscopy. The nano-barcodes may be any molecule or complex that is distinguishable by scanning probe microscopy (SPM), such as carbon nanotubes, fullerenes, submicrometer metallic barcodes, nanoparticles or quantum dots. Where the probes are oligonucleotides, adjacent coded probes hybridized to a target nucleic acid may be ligated together before alignment and scanning probe microscopy (SPM) analysis. Compositions comprising coded probes are also disclosed herein. Systems for biomolecule analysis may comprise a scanning probe microscopy (SPM) instrument and at least one coded probe attached to a surface.

Claims

1. A method comprising:

a) obtaining a plurality of coded probes, each of the coded probes comprising a probe molecule attached to at least one nano-barcode, and at least two of the coded probes comprise two or more identifiably different nano-barcodes that can generate different detectable signals wherein the nano-barcode is selected from the group consisting of carbon nanotubes, fullerenes, submicrometer metallic barcodes, nanoparticles, quantum dots, combinations thereof, and the nano-barcodes made from nano-tag elements;

b) contacting one or more target molecules in a sample with the coded probes wherein the coded probes comprise oligonucleotides and bind to different locations on the target molecules;

c) ligating the coded probes that are adjacent one another on the target molecules to form ligated coded probes and aligning the ligated coded probes on a substrate surface by molecular combing using microfludic channels and forming organized coded probes wherein the ligated coded probes are aligned in the direction of microfluidic flow in the microfluidic channels;

d) identifying the organized coded probes; and

e) detecting the one or more target molecules based on the organized coded probes.

2. The method of claim 1, wherein the target molecule is a nucleic acid.

3. The method of claim 2, further comprising, contacting a library of coded probes comprising all possible nucleic acid sequences for a particular length of oligonucleotide with the one or more target molecules.

4. The method of claim 2, wherein the nucleic acid is attached to a surface.

5. The method of claim 2, further comprising separating the ligated coded probes from the nucleic acid and non-ligated coded probes.

6. The method of claim 1, wherein the organized coded probes are identified by scanning probe microscopy.

7. The method of claim 1, wherein the organized coded probes are identified by an equipment selected from the group consisting of atomic force microscopy, scanning tunneling microscopy, lateral force microscopy, chemical force microscopy, force modulation imaging microscopy, magnetic force microscopy, high frequency magnetic force microscopy, magnetoresistive sensitivity mapping microscopy, electric force microscopy, scanning capacitance microscopy, scanning spreading resistance microscopy, tunneling atomic force microscopy and conductive atomic force microscopy.

8. The method of claim 1, wherein the organized coded probes aligned on the substrate surface are identified by scanning probe microscopy.

9. The method of claim 2, further comprising determining the sequences of the oligonucleotides that bind to the nucleic acid.

10. The method of claim 9, further comprising determining the sequence of the nucleic acid based on the sequences of the oligonucleotides that bind to the nucleic acid.

11. The method of claim 2, further comprising identifying the nucleic acid based on the coded probes that bind to the nucleic acid.

12. The method of claim 1, wherein the target molecule is a protein, a peptide, a glycoprotein, a lipoprotein, a nucleic acid, a polynucleotide, or an oligonucleotide.

13. The method of claim 12, wherein the sample further comprising two or more target molecules and the target molecules in the sample are analyzed at the same time.

14. The method of claim 12, wherein the sample further comprising two or more target molecules and the target molecules of the same type are analyzed at the same time.

15. The method of claim 1, wherein the coded probes are further aligned on the substrate surface by free flow electrophoresis.

16. A method comprising:

a) obtaining a plurality of coded probes, each of the coded probes comprising a probe molecule attached to at least one nano-barcode, and at least two of the coded probes comprise two or more identifiably different nano-barcodes that can generate different detectable signals wherein the nano-barcode is selected from the group consisting of carbon nanotubes, fullerenes, submicrometer metallic barcodes, nanoparticles, quantum dots, combinations thereof and the nano-barcodes made from nano-tag elements;

b) contacting one or more target molecules with the coded probes wherein the coded probes comprise oligonucleotides and bind to different locations on the target molecules;

c) ligating the coded probes that are adjacent one another on the target molecules to form ligated coded probes and aligning the ligated coded probes on a substrate surface by molecular combing using microfluidic channels and forming aligned coded probes wherein the ligated coded probes are aligned in the direction of microfluidic flow in the microfluidic channels;

d) identifying the aligned coded probes using scanning probe microscopy; and

e) detecting the one or more target molecules based on the aligned coded probes.

17. The method of claim 16, wherein the scanning probe microscopy is selected from the group consisting of atomic force microscopy, scanning tunneling microscopy, lateral force microscopy, chemical force microscopy, magnetic force microscopy, high frequency. magnetic force microscopy, electric force microscopy, scanning capacitance microscopy, scanning spreading resistance microscopy, tunneling atomic force microscopy and conductive atomic force microscopy.

18. The method of claim 16, wherein the target molecule is a nucleic acid.

19. The method of claim 18, further comprising determining at least part of the sequence of the nucleic acid based on the aligned coded probes.

20. The method of claim 16, further comprising separating the bound coded probes from the target molecules after the coded probes are aligned on the substrate surface.

21. The method of claim 16, wherein the coded probes are further aligned on the substrate surface by free flow electrophoresis.

22. A method comprising:

a) obtaining a plurality of coded probes, each of the coded probes comprising a probe molecule attached to at least one nano-barcode, and at least two of the coded probes comprise two or more identifiably different nano-barcodes that can generate different detectable signals wherein the nano-barcode is selected from the group consisting of carbon nanotubes, fullerenes, submicrometer metallic barcodes, nanoparticles, ciuantum dots, combinations thereof and the nano-barcodes made from nano-tag elements;

b) contacting one or more target molecules with the coded probes and forming binding complexes wherein the coded probes comprise oligonucleotides;

c) aligning the coded probes of the binding complexes on a surface by free flow electrophoresis and forming organized coded probes;

d) identifying the organized coded probes; and

e) detecting the one or more target molecules based on the organized coded probes.

23. A method comprising:

a) obtaining a plurality of coded probes, each of the coded probes comprising a probe molecule attached to at least one nano-barcode, and at least two of the coded probes comprise two or more identifiably different nano-barcodes that can generate different detectable signals wherein the nano-barcode is selected from the group consisting of carbon nanotubes, fullerenes, submicrometer metallic barcodes, nanoparticles, quantum dots, combinations thereof and the nano-barcodes made from nano-tag elements;

b) contacting one or more target molecules with the coded probes wherein the coded probes bind to the target molecules and form binding complexes, and wherein the coded probes comprise olgonucleotides;

c) aligning the coded probes of the binding complexes on a surface by free flow electrophoresis and forming aligned coded probes;

d) identifying the aligned coded probes using scanning probe microscopy; and

e) detecting the one or more target molecules based on the aligned coded probes.