Systems for detecting and quantifying nucleic acids
This invention is based, in part, on our discovery of an essentially one-step, label-free system comprising a sensing unit having a redox current reporter and a nucleic acid sequence complementary to that of a target nucleic acid of interest or sufficiently complementary to that of the target nucleic acid or a sequence therein to specifically bind the target nucleic acid. The sensing unit is bound to an electroconductive substrate (e.g., a carbon- or metal-containing microelectrode (e.g., a gold microelectrode)), and the system includes a signal amplification mechanism that does not rely upon a redox enzyme and thereby overcomes a fundamental limitation of microelectrode DNA sensors that fail to generate detectable current in the presence of only small amounts of a target nucleic acid.
1. A system for detecting a target nucleic acid in a sample, the system comprising
an electroconductive substrate;
a sensing unit that is bound to the substrate, wherein the sensing unit comprises
a redox current reporter and
a sequence-specific nucleic acid,
wherein the sequence-specific nucleic acid comprises a nucleic acid sequence that is sufficiently complementary to that of the target nucleic acid or a sequence therein to specifically bind the target nucleic acid,
wherein the sequence-specific nucleic acid is a single nucleic acid strand, is bound to the substrate, and is not bound to the substrate via a separate nucleic acid strand,
wherein the redox current reporter is linked to the sequence-specific nucleic acid; and
a coreactant.
2. The system of claim 1 , wherein the target nucleic acid is a microRNA (miRNA) or a precursor thereof.
3. The system of claim 1 , wherein the electroconductive substrate comprises a carbon- or metal-containing microelectrode.
4. The system of claim 3 , wherein the electroconductive substrate is fashioned as a microelectrode having a radius or dimension of about 0.1-100 μm, a nanoelectrode having a radius or dimension below 0.1 micron, or a macroelectrode having a radius or dimension above 100 micron.
5. The system of claim 1 , wherein the sensing unit is covalently bound to the substrate.
6. The system of claim 1 , wherein the sensing unit is bound to the substrate through a thiolate moiety.
7. The system of claim 1 , further comprising alkanethiolate moieties bound to the substrate to passivate the system and thereby reduce non-specific signals.
8. The system of claim 1 , wherein the redox current reporter comprises a molecule capable of undergoing oxidation, thereby transferring electrons to the substrate and generating an oxidized redox current reporter.
9. The system of claim 1 , wherein the redox current reporter comprises a molecule capable of undergoing reduction, thereby capturing electrons from the substrate and generating a reduced redox current reporter.
10. The system of claim 9 , wherein the coreactant is capable of oxidizing the reduced redox current reporter.
11. The system of claim 1 , w8herein the nucleic acid sequence is 17-27 nucleotides in length.
12. The system of claim 1 further comprising a common buffer in which the coreactant is contained.
13. The system of claim 1 , wherein the coreactant is a reductant selected from the group consisting of oxalic acid (C 2 H 2 O 4 ), formic acid (HCOOH), ascorbic acid (C 6 H 8 O 8 ), a compound comprising an Sn 2+ ion or Fe 2+ ion, hydrazine, tris-(2-carboxyethyl) phosphine hydrochloride (TCEP), and any other reagent that will reduce an oxidized redox current reporter; or an oxidant selected from the group consisting of oxygen, hydrogen peroxide and other reactive oxygen species, a compound comprising an Fe 3+ ion, a compound comprising ClO 4 − , BO 3 − , MnO 4 − , SO 5 2− , S 2 O 8 2− , HSO 5 − , ClO 2 − or other halogen-containing anions, and any other reagent that will oxidize a reduced redox current reporter.
14. The system of claim 1 , wherein the sensing unit lacks a redox enzyme.
15. The system of claim 1 , wherein the system is configured for high throughput screening of a plurality of nucleic acids.
16. The system of claim 15 , wherein the system comprises a plurality of sensing units, with a first sensor designed to detect a first nucleic acid and a second sensor designed to detect a second nucleic acid, wherein levels of expression of the first and second nucleic acids together signify the presence of a disease state.
17. A method of detecting a target nucleic acid in a sample, the method comprising:
providing a sample comprising nucleic acids obtained from a subject or from a patient; and
exposing the sample to the system of claim 1 .
18. A method of making the system of claim 1 , the method comprising
(a) providing an electroconductive substrate;
(b) immersing the substrate in a solution comprising sensing units for a time sufficient to allow the sensing units to self-assemble on the surface of the substrate, thereby generating a probe-functionalized substrate;
(c) immersing the probe-functionalized substrate in a solution comprising passivating agents for a time sufficient to allow the agents to self-assemble on the surface of the substrate.
19. The method of claim 18 , wherein the sensing unit comprises a sulfhydryl group, alkyne, or any functional group that provides precursors to bind to the electroconductive substrate; wherein the passivating agents comprise a sulfhydryl group or are an alkanethiol; or wherein the step of immersing the probe-functionalized substrate in a solution comprising inert thiol moieties further comprises heating and cooling the solution.