Nano-scale biosensors
View Patent ↗Devices, systems, and methods for detecting nucleic acid hybridization, including single nucleic base mutations at low concentrations, are disclosed, using surface-tethered hairpin loop oligonucleotide probes and metal-nanoparticles conjugated to a hybridization detection sequence that is capable of binding the stem region of the opened hairpin loop oligonucleotide probe, without the use of labeling or target modification and capable of recycling.
1. A device, comprising:
a thermally responsive, electrically insulating substrate;
at least one heating element; and
a first detecting unit, comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of first oligonucleotide probes attached to said substrate in said nanogap;
wherein said first oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said first oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded.
2. A device of claim 1 ,
wherein said first oligonucleotide probes form a self-assembled monolayer.
3. A device of claim 1 ,
wherein said thermally responsive, electrically insulating substrate is silicon, silicon dioxide, or a combination thereof.
4. A device of claim 1 , further comprising:
a plurality of additional heating elements capable of forming a temperature gradient.
5. A device of claim 1 ,
wherein said heating element is embedded in said substrate.
6. A device of claim 1 ,
wherein said heating element comprises gold.
7. A device of claim 1 ,
wherein said first detecting unit is located on the surface of said substrate.
8. A device of claim 1 ,
wherein said first and second electrodes comprise a metal selected from the group consisting of gold, silver, titanium, copper, or a combination thereof.
9. A device of claim 1 ,
wherein said nanogap is formed by electromigration.
10. A device of claim 1 ,
wherein said nanogap is about 10 nm to about 500 nm.
11. A device of claim 1 ,
wherein said first oligonucleotide probes are covalently attached to said substrate.
12. A device of claim 1 ,
wherein each of said first oligonucleotide probes comprise:
an optional spacer having about one nucleotide base to about 20 nucleotide bases;
a nucleotide loop having about 3 nucleotide bases to about 100 nucleotide bases; and
a base pair stem having about 3 nucleotide base pairs to about 20 nucleotide base pairs.
13. A device of claim 1 ,
wherein each of said first oligonucleotide probes comprise:
a spacer having about 3 nucleotide bases;
a nucleotide loop having about 12 nucleotide bases; and
a base pair stem having about 6 nucleotide base pairs.
14. A device of claim 1 , further comprising:
a plurality of second detecting units, comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of second oligonucleotide probes attached to said substrate in said nanogap;
wherein said second oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence;
wherein said second oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
wherein said second oligonucleotide probes are the same or different from said first oligonucleotide probes in said first detecting unit; and
wherein said second oligonucleotide probes are the same or different from other second oligonucleotide probes in said plurality of second detecting units.
15. A device of claim 1 , further comprising:
a plurality of microfluidic channels; and
an optional cover.
16. A device of claim 1 ,
wherein said at least one heating element is located in a first layer; and
wherein said first electrode and said second electrodes are located in a second layer.
17. A system, comprising:
a device of claim 1 ; and
a plurality of nanoparticle reporter conjugates;
wherein said nanoparticle reporter conjugates comprise at least one nanoparticle and a single-stranded oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probe; and
wherein said nanoparticle is a metal, semiconductor, or magnetic colloidal particle.
18. A system of claim 17 ,
wherein said single-stranded oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probe comprises about 3 nucleotide bases to about 80 nucleotide bases.
19. A system of claim 17 ,
wherein said single-stranded oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probe comprises about 7 nucleotide bases.
20. A system, comprising:
a device of claim 14 ; and
a plurality of first nanoparticle reporter conjugates; and
a plurality of at least one second nanoparticle reporter conjugates;
wherein said first nanoparticle reporter conjugates comprise at least one nanoparticle and a single-stranded oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probes;
wherein said nanoparticle in said first nanoparticle reporter conjugate is a metal, semiconductor, or magnetic colloidal particle;
wherein said second nanoparticle reporter conjugates comprise at least one nanoparticle and a single-stranded oligonucleotide complementary to at least a portion of said stem of said second oligonucleotide probes;
wherein said nanoparticle in said second nanoparticle reporter conjugate is a metal, semiconductor, or magnetic colloidal particle;
wherein said second nanoparticle reporter conjugates are the same or different from said first nanoparticle reporter conjugates; and
wherein said second nanoparticle reporter conjugates are the same or different from said other second nanoparticle reporter conjugates.
21. A system of claim 20 ,
wherein said single-stranded oligonucleotide complementary to at least a portion of said stem of said hairpin loop probe comprises about 3 nucleotide bases to about 80 nucleotide bases.
22. A system of claim 20 ,
wherein said single-stranded oligonucleotide complementary to at least a portion of said stem of said hairpin loop probe comprises about 7 nucleotide bases.
23. A system of claim 17 or 20 , further comprising:
an electrical reading device for interrogating said device of claim 1 .
24. A system of claim 23 ,
wherein said electrical reading device is portable.
25. A method for detecting nucleic acid hybridization, comprising:
providing a device, comprising:
a thermally responsive, electrically insulating substrate;
at least one heating element; and
a first detecting unit, comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of first oligonucleotide probes attached to said substrate in said nanogap;
wherein said first oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said first oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
providing a solution comprising at least one buffer and single-stranded oligonucleotide target under hybridizing conditions;
wherein said single-stranded oligonucleotide target hybridizes at least some of said first oligonucleotide probes to form elongated oligonucleotide probes;
providing a plurality of first nanoparticle reporter conjugates under hybridizing conditions;
wherein said first nanoparticle reporter conjugates comprise at least one nanoparticle and an oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probes;
wherein said nanoparticle in said first nanoparticle reporter conjugate is a metal, semiconductor, or magnetic colloidal particle;
applying a voltage drop across said electrodes; and
measuring a change in conductivity, resistivity, capacitance, or impedance across said electrodes at known locations to determine perfect complementarity of said oligonucleotide target to said first oligonucleotide probes.
26. A method of claim 25 ,
wherein said voltage drop is applied as direct current.
27. A method of claim 25 ,
wherein said voltage drop is applied as alternating current.
28. A method of claim 25 ,
wherein said measuring step measures an increase in conductivity across said electrodes at known locations to determine perfect complementarity of said oligonucleotide target to said first oligonucleotide probes.
29. A method of claim 25 ,
wherein said single-stranded oligonucleotide target is prepared by heating a solution comprising double-stranded oligonucleotide target.
30. A method of claim 25 , further comprising:
washing to remove unhybridized components from said detecting unit.
31. A method of claim 25 , further comprising:
heating said device to remove said hybridized targets and said hybridized nanoparticle reporter conjugates from said probe to permit recycling of said detecting unit.
32. A method of claim 25 , further comprising:
heating a solution comprising double stranded oligonucleotide target to form said solution comprising single-stranded oligonucleotide target.
33. A method of claim 25 , further comprising:
forming a temperature gradient to focus said single stranded oligonucleotide target at said detecting unit.
34. A method of claim 25 , further comprising:
reversing the polarity of said voltage drop to remove unbound components or nonspecifically bound components from said detecting unit.
35. A method of claim 25 , further comprising:
providing, in addition to said first detecting unit, a plurality of additional detecting units, each additional detecting unit comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of second oligonucleotide probes attached to said substrate in said nanogap;
wherein said second oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said second oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded
wherein said second oligonucleotide probes are the same or different from said first oligonucleotides in said first detecting unit; and
wherein said second oligonucleotide probes are the same or different from other second oligonucleotide probes in said plurality of second detecting units;
providing a plurality of at least one second nanoparticle reporter conjugates under hybridizing conditions;
wherein said second nanoparticle reporter conjugates comprise at least one nanoparticle and an oligonucleotide complementary to at least a portion of said stem of said second oligonucleotide probes;
wherein said nanoparticle in said second nanoparticle reporter conjugate is a metal, semiconductor, or magnetic colloidal particle;
wherein said second nanoparticle reporter conjugates are the same or different from said first nanoparticle reporter conjugates;
wherein said second nanoparticle reporter conjugates are the same or different from said other second nanoparticle reporter conjugates;
wherein said measuring step is carried out in parallel or sequentially for said first detecting unit and said plurality of said additional detecting units.
36. A method for detecting nucleic acid hybridization, comprising:
providing a device, comprising:
a thermally responsive, electrically insulating substrate;
at least one heating element; and
a first detecting unit, comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of first oligonucleotide probes attached to said substrate in said nanogap;
wherein said first oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said first oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
providing a solution comprising at least one buffer and single-stranded oligonucleotide target under hybridizing conditions;
wherein said single-stranded oligonucleotide target hybridizes at least some of said first oligonucleotide probes to form elongated oligonucleotide probes;
providing a plurality of first reporter conjugates under hybridizing conditions;
wherein said first reporter conjugates comprise an oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probes;
reversibly exchanging an imino proton in each base pair of said first reporter conjugate or said stem of said first oligonucleotide probes with a metal ion selected from the group consisting of gold ion, silver ion, platinum ion, and copper ion;
applying a voltage drop across said electrodes; and
measuring a change in conductivity, resistivity, capacitance, or impedance across said electrodes at known locations to determine perfect complementarity of said oligonucleotide target to said first oligonucleotide probes.
37. A method of claim 36 , further comprising:
providing, in addition to said first detecting unit, a plurality of additional detecting units, each additional detecting unit comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of second oligonucleotide probes attached to said substrate in said nanogap;
wherein said second oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said second oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
wherein said second oligonucleotide probes are the same or different from said first oligonucleotides in said first detecting unit; and
wherein said second oligonucleotide probes are the same or different from other second oligonucleotide probes in said plurality of second detecting units;
providing a plurality of at least one second reporter conjugates under hybridizing conditions;
wherein said second reporter conjugates comprise an oligonucleotide complementary to at least a portion of said stem of said second oligonucleotide probes;
wherein said second reporter conjugates are the same or different from said first nanoparticle reporter conjugates;
wherein said second reporter conjugates are the same or different from said other second nanoparticle reporter conjugates;
reversibly exchanging an imino proton in each base pair of said second reporter conjugate or said stem of said second oligonucleotide probes with a metal ion selected from the group consisting of gold ion, silver ion, platinum ion, and copper ion;
wherein said measuring step is carried out in parallel or sequentially for said first detecting unit and said plurality of said additional detecting units.
38. A method for detecting nucleic acid hybridization, comprising:
providing a device, comprising:
a thermally responsive, electrically insulating substrate;
at least one heating element; and
a first detecting unit, comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of first oligonucleotide probes attached to said substrate in said nanogap;
wherein said first oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said first oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
providing a solution comprising at least one buffer and single-stranded oligonucleotide target under hybridizing conditions;
wherein said single-stranded oligonucleotide target hybridizes at least some of said first oligonucleotide probes to form elongated oligonucleotide probes;
providing a plurality of first nanoparticle reporter conjugates under hybridizing conditions to form a double stranded nucleic acid sequence;
wherein said first nanoparticle reporter conjugates comprise an oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probes;
vectorially depositing silver on said double stranded nucleic acid sequence;
applying a voltage drop across said electrodes; and
measuring a change in conductivity, resistivity, capacitance, or impedance across said electrodes at known locations to determine perfect complementarity of said oligonucleotide target to said first oligonucleotide probes.
39. A method of claim 38 ,
wherein said vectorially depositing step comprises:
ion exchanging silver ions on said double stranded nucleic acid sequence;
reducing said silver ions; and
developing silver aggregates on said double stranded nucleic acid sequence.
40. A method of claim 38 , further comprising:
providing, in addition to said first detecting unit, a plurality of additional detecting units, each additional detecting unit comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of second oligonucleotide probes attached to said substrate in said nanogap;
wherein said second oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence;
wherein said second oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
wherein said second oligonucleotide probes are the same or different from said first oligonucleotides in said first detecting unit; and
wherein said second oligonucleotide probes are the same or different from other second oligonucleotide probes in said plurality of second detecting units;
providing a plurality of at least one second reporter conjugates under hybridizing conditions;
wherein said second reporter conjugates comprise an oligonucleotide complementary to at least a portion of said stem of said second oligonucleotide probes;
wherein said second reporter conjugates are the same or different from said first nanoparticle reporter conjugates;
wherein said second reporter conjugates are the same or different from said other second nanoparticle reporter conjugates; and
vectorially depositing silver on said double stranded nucleic acid sequence;
wherein said measuring step is carried out in parallel or sequentially for said first detecting unit and said plurality of said additional detecting units.
41. A method for detecting nucleic acid hybridization, comprising:
providing a device, comprising:
a thermally responsive, electrically insulating substrate;
at least one heating element; and
a first detecting unit, comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of first oligonucleotide probes attached to said substrate in said nanogap;
wherein said first oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence; and
wherein said first oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
providing a solution comprising at least one buffer and single-stranded oligonucleotide target under hybridizing conditions;
wherein said single-stranded oligonucleotide target hybridizes at least some of said first oligonucleotide probes to form elongated oligonucleotide probes;
providing a plurality of first reporter molecules under hybridizing conditions to form a double stranded oligonucleotide-stem complex;
wherein said first reporter molecules comprise an oligonucleotide complementary to at least a portion of said stem of said first oligonucleotide probes;
providing a solution comprising first nanoparticle polypeptide conjugates;
wherein said first nanoparticle polypeptide conjugates comprise at least one nanoparticle and a polypeptide that binds to said double stranded oligonucleotide-stem complex;
wherein said nanoparticle in said first nanoparticle polypeptide conjugates is a metal, semiconductor, or magnetic colloidal particle;
applying a voltage drop across said electrodes; and
measuring a change in conductivity, resistivity, capacitance, or impedance across said electrodes at known locations to determine perfect complementarity of said oligonucleotide target to said first oligonucleotide probes.
42. A method of claim 41 , further comprising:
providing, in addition to said first detecting unit, a plurality of additional detecting units, each additional detecting unit comprising:
a first electrode and a second electrode separated by a nanogap; and
a plurality of second oligonucleotide probes attached to said substrate in said nanogap;
wherein said second oligonucleotide probes are in a hairpin loop formation and have the same nucleic acid sequence;
wherein said second oligonucleotide probes comprise an optional spacer, a loop, and a stem region, said stem region being double-stranded;
wherein said second oligonucleotide probes are the same or different from said first oligonucleotides in said first detecting unit; and
wherein said second oligonucleotide probes are the same or different from other second oligonucleotide probes in said plurality of second detecting units;
providing a plurality of second reporter molecules under hybridizing conditions to form a double stranded oligonucleotide-stem complex;
wherein said second reporter molecules comprise an oligonucleotide complementary to at least a portion of said stem of said second oligonucleotide probes;
providing a solution comprising second nanoparticle polypeptide conjugates;
wherein said second nanoparticle polypeptide conjugates comprise at least one nanoparticle and a polypeptide that binds to said double stranded oligonucleotide-stem complex;
wherein said nanoparticle in said second nanoparticle polypeptide conjugates is a metal, semiconductor, or magnetic colloidal particle;
wherein said second reporter molecules are the same or different from said first reporter molecules;
wherein said second reporter molecules are the same or different from other second reporter molecules;
wherein said measuring step is carried out in parallel or sequentially for said first detecting unit and said plurality of said additional detecting units.