Colorimetric readout of hybridization chain reaction

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates generally to the use of calorimetric testing using nano-gold particles to identify the presence of one or more analytes in a sample and more particularly to the use of hybridization chain reaction (HCR) to create a visual signal in the presence of target analytes.

2. Description of the Related Art

Single stranded DNA is a versatile material that can be programmed to self-assemble into complex structures driven by the free energy of base pair formation. Synthetic DNA machines can be powered by strand displacement interactions initiated by the sequential introduction of auxiliary DNA fuel strands. Typically, various DNA strands begin to associate as soon as they are mixed together. Catalytic fuel delivery proves a conceptual approach to powering autonomous DNA machines by storing potential energy in loops that are difficult to access kinetically except in the presence of a catalyst strand.

Hybridization chain reaction (HCR) is a method for the triggered chain hybridization of nucleic acid molecules starting from stable, monomer hairpins or other more complicated nucleic acid structures. HCR is described in U.S. patent application Ser. No. 11/087,937, filed Mar. 22, 2005, which is hereby incorporated by reference in its entirety. In the simplest version of this process, stable monomer hairpins undergo a chain reaction of hybridization events to form a nicked helix when triggered by a nucleic acid initiator strand. A fundamental principle behind HCR is that short loops are resistant to invasion by complementary single-stranded nucleic acids. This stability allows for the storage of potential energy in the form of loops. Potential energy is released when a triggered conformational change allows the single stranded bases in the loops to hybridize with a complementary strand.

Nano-gold based colorimetric systems have been used for detection of nucleic acid sequences. See, for example, R. Elghanian, J. I. Storhoff, R. C. Mucic, R. L. Letsinger, and C. A. Mirkin. Selective colorimetric detection of polynucleotides based on the distance-dependent optical properties of gold nanoparticles. Science, 277(5329):1078-1081, 1997 and J. W. Liu and Y. Lu. A colorimetric lead biosensor using DNAzyme-directed assembly of gold nanoparticles. J. Am. Chem. Soc., 125(22):66426643, 2003, each of which is hereby incorporated by reference. Gold particles functionalized by thiolated DNA strands can be aggregated via complementary strand hybridization, shifting the sample color from red to blue. (U. Storhoff, R. Elghanian, R. C. Mucic, C. A. Mirkin, and R. L. Letsinger. One-pot calorimetric differentiation of polynucleotides with single base imperfections using gold nanoparticles. J. Am. Chem. Soc., 120:1959-1964, 1998, incorporated herein by reference).

SUMMARY OF THE INVENTION

In one aspect, methods for detecting an analyte in a sample by calorimetric hybridization chain reaction are provided. HCR monomers polymerize in the presence of an analyte and polymerized HCR products are detected by a color change in nano-gold particles associated with the polymers. The nano-gold particles may be conjugated to one or more of the HCR monomers or may be part of a detection component that is able to associate with the HCR polymers but not the unpolymerized monomers.

In some embodiments, a sample to be tested for the presence of an analyte is contacted with one or more first metastable HCR monomers. The first HCR monomers are each conjugated to one or more nano-gold particles. Preferably the nano-gold particles are from about 1 to about 250 nm in diameter, more preferably from about 10 to about 50 nm in diameter.

The sample is contacted with one or more second metastable HCR monomers comprising a region complementary to a portion of the first monomer, such that the first and second HCR monmers polymerize in the presence of the analyte to be detected. The second monomers may also be conjugated to nano-gold particles. A color change in the nano-gold particles identifies the presence of polymerized HCR monomers, and thus indicates the presence of the analyte in the sample. The color change is brought about by the change in proximity of the nano-gold particles upon polymerization of the monomers. In preferred embodiments, polymerization of the HCR monomers leads to aggregation of the nano-gold particles and a color shift from red to blue.

In some embodiments the sample is obtained from a patient and the analyte to be detected is associated with a disease, disorder or condition, such as with a pathogen.

In another aspect, methods of identifying an aggregated nucleic acid structure are provided. A first nucleic acid construct is provided comprising a duplex region, a first loop region and an initiator complement region that is substantially complementary to an initiation region of an initiator nucleic acid. A second nucleic acid is provided comprising a second duplex region, at least one second loop region and a first nucleic acid complementary region that is substantially complementary to the initiator complement region of the first monomer. Binding of an initiator nucleic acid to the first nucleic acid construct leads to aggregation of the first and second monomers to form an aggregated nucleic acid structure. The initiator may be the analyte of interest, such as a nucleic acid that is to be detected. Alternatively, the initiator may comprise a recognition molecule, such as an aptamer, and the initiator is provided to the sample. In the presence of analyte, such as a polypeptide, the initiator can undergo a conformational change such that the initiation region is able to bind to the initiator complement region of the first nucleic acid construct.

In some embodiments third and fourth nucleic acid constructs are included in the HCR reactions, and these constructs are incorporated in the aggregated nucleic acid structure formed in the presence of the analyte of interest.

A detection component comprising nano-gold particles is provided and aggregated nucleic acid structures are identified by observing a color change in the nano-gold particles. The detection component can be provided at the same time as the other HCR components or can be provided subsequently. In some embodiments the detection component is able to hybridize to the aggregated nucleic acid structure and preferably comprises a nucleic acid that is complementary to a portion of the first and/or second nucleic acid constructs. In other embodiments the detection component comprises a DNA binding reagent and is able to bind to the aggregated nucleic acid construct but not to the first and second nucleic acid constructs prior to aggregation.

In a further aspect of the invention, kits are provided that can be used for the detection of an analyte in a sample. The kits preferably comprise a first metastable nucleic acid monomer comprising an initiator complement region and a second metastable nucleic acid monomer comprising a propagation region that is substantially complementary to a portion of the first nucleic acid. A detection component comprising a nano-gold particle may be provided in the kit. However, in some embodiments the first and/or second nucleic acid monomers serve as the detection component and are conjugated to one or more nano-gold particles.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 schematically illustrates one embodiment of an HCR system. Each letter represents a segment of nucleic acids. Letters marked with a* are complementary to the corresponding unmarked letter.

FIG. 1A shows two hairpins, labeled H1 and H2, that are metastable in the absence of initiator I. The hairpins comprise sticky ends ‘a’ and ‘c*’, respectively. Potential energy is stored in the hairpin loops.

FIG. 1B shows how a single initiator strand ‘I’ can nucleate or bind to the sticky end of H1 and displace one arm to open the hairpin. This frees up the bases that were trapped in the hairpin, allowing them to perform a similar displacement reaction on H2.

As illustrated in FIG. 1C, the newly exposed c region of H1 nucleates at the sticky end of H2 and opens the hairpin to expose a region on H2 (a*) that is identical in sequence to the initiator I. As a result, each copy of I can propagate a chain reaction of hybridization events between alternating H1 and H2 hairpins to form a nicked double helix, thereby amplifying the signal of initiator binding. The process can continue until the monomers (H1 and H2) are exhausted. At each step, energy is gained from the hybridization of ‘a’ or ‘c’. The reactions diagrammed in FIG. 1 have been successfully carried out and are summarized in FIG. 1D.

FIG. 1D illustrates the results of an HCR reaction and the effect of initiator concentration on amplification. Lanes 2-7: Six different concentrations of initiator were used (0.00, 10.00, 3.20, 1.00, 0.32 and 0.10 μM, respectively) in a 1 μM mixture of H1 and H2. Lanes 1 and 8 were DNA markers with 100-bp and 500-bp increments respectively.

FIG. 1E illustrates HCR kinetics monitored by substituting a fluorescently labeled base in the sticky end of an HCR monomer. Here 2-aminopurine (2AP) was substituted for A (base 3) in the sticky end of H1. The hairpin monomers H1 and H2 did not hybridize prior to triggering by initiator ((H1^2AP+1.2×H2 for 24 hours+0.5× initiator), red). The same quenched baseline was achieved without HCR by adding excess initiator to H1^2APin the absence of H2 (H1^2AP+4.0× initiator, green). Addition of insufficient initiator to H1^2APprovided only partial quenching (H1^2AP+0.5× initiator (blue), demonstrating that HCR, and not initiator alone, was responsible for exhausting the supply of H12AP monomer.

FIG. 2 illustrates an embodiment in which HCR utilizing two monomer pairs produces quadratic signal amplification. FIG. 2A illustrates two hairpin monomers Q1 and Q2 that are metastable in the absence of initiator IQ. As shown in FIG. 2B, binding of IQ leads to a strand displacement interaction that exposes sticky end fe*b*. This single stranded region then nucleates at the f* sticky end of Q2, and a subsequent branch migration exposes segments cb*d* and e* as shown in FIG. 2C. The d*e* region initiates the next Q1 molecule, leading to amplification in one direction, while the exposed cb* region initiates a second HCR reaction involving monomers H1 and H2 (FIG. 1). As illustrated in FIG. 2D, the resulting branched polymer has a Q1/Q2 main chain with H1/H2 side chains branching off at each Q2 segment.

FIG. 3 illustrates a pair of monomers (E1 and E2) that can be used in combination with at least one other pairs of monomers to achieve exponential amplification by HCR. In the presence of cb*, E1 and E2 form a linear chain that includes periodic single stranded d*e* regions. The initiator sequence for E1/E2 matches the periodic single stranded region produced by Q1/Q2 and vice versa. Consequently, a mixture of Q1, Q2, E1 and E2 plus either initiator (cb* or d*e*) will lead to the formation of a structure in which each branch of the polymer is itself a branched polymer. Sustained growth will ultimately decrease to cubic amplification.

FIGS. 4A-E illustrate another embodiment for HCR with exponential growth. Eight different strands are used in this embodiment. Strand one (1) is the ‘hub’ of the system and has an exposed, single-stranded region joining two hairpins (FIG. 4A). When the initiator (2) binds, it creates a long helix with one sticky end on each side. The two sticky ends generated by the initiated ‘hub’ bind with strands (3) and (6), respectively (FIGS. 4B and C). Next, auxiliary strands (4) and (7) bind to previously protected bulge loops (FIGS. 4D and E), and expose two hairpin regions. These hairpins then bind to strands (5) and (8), respectively, to generate sticky ends similar to the initiator molecule (2). Thus, each initiator produces two new initiators, leading to exponential growth. As a side note, two subsets of strands (1,2,3,4,5) and (1,2,6,7,8) produce linear systems in the absence of the other strands.

FIG. 5A illustrates an aptamer HCR trigger mechanism for the detection of ATP. Binding of the DNA aptamer to ATP induces a conformation change that exposes a sticky end.

FIG. 5B shows an agarose gel demonstrating ATP detection via HCR.

FIG. 6 illustrates a self-complementary hairpin with an interior loop that is a double helix (dotted lines). DNA hairpin can also exist as a dimer with an interior loop. One possible concern is that the interior loops may be easier to invade than the corresponding hairpins. To prevent this side reaction, self-complementary hairpins would convert the interior loop to a simple double helix (dotted lines). However, this added precaution may not be necessary.

FIG. 7A illustrates a colorimetric HCR scheme employing the Q1, Q2 and I strands of the quadratic HCR scheme in FIG. 2. Periodic single stranded regions (for example, cb* in FIG. 2) provide binding sites for DNA functionalized gold nano-particle.

FIG. 7B illustrates the results of calorimetric HCR studies. In the absence of analyte (−) a red sample color was observed. In the presence of a target analyte a color shift from red to blue was observed by TLC spot test.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

Hybridization Chain Reaction (HCR) is a novel method for the triggered hybridization of nucleic acid molecules starting from metastable monomer hairpins or other metastable nucleic acid structures. Dirks, R. and Pierce, N. Proc. Natl. Acad. Sci. USA 101(43): 15275-15278 (2004), incorporated herein by reference in its entirety. HCR does not require any enzymes and can operate isothermally.

In one embodiment of HCR, two or more metastable monomer hairpins are used. The hairpins preferably comprise loops that are protected by long stems. The loops are thus resistant to invasion by complementary single-stranded nucleic acids. This stability allows for the storage of potential energy in the loops. Potential energy is released when a triggered conformational change allows the single-stranded bases in the loops to hybridize with a complementary strand, preferably in a second hairpin monomer.

Each monomer is caught in a kinetic trap, preventing the system from rapidly equilibrating. That is, pairs of monomers are unable to hybridize with each other in the absence of an initiator. Introduction of an initiator strand causes the monomers to undergo a chain reaction of hybridization events to form a nicked helix (see FIGS. 1A-C). HCR can be used, for example, to detect the presence of an analyte of interest in a sample.

Methods are provided herein for creating a visual signal, preferably a color change to indicate detection of one or more analytes by HCR. Such calorimetric signaling can improve efficiency and allow for portability, for example by allowing visualization of a signal with the naked eye, thus not requiring any instrument for detection (although an instrument may be used in some embodiments). Colorimetric testing for the presence and/or amount of one or more particular analytes in a sample can be used, for example, in consumer kits for analyte detection, in a primary care setting and in remote areas.

In some embodiments, one or more components of the HCR system are attached to a colorimetric indicator, preferably a nanometer scale gold particle (nano-gold), such that upon HCR polymerization, the nano-gold particles aggregate and undergo a color change. In other embodiments, nano-gold particles are able to bind to HCR components upon polymerization, leading to aggregation of the nano-gold particles and an associated color change. Thus, upon detection of an analyte of interest, the calorimetric indicator is activated. Preferably, the color change is visible to the naked eye. In other embodiments, the color change is determined by a method such as thin layer chormotograph (TLC) or with the aid of an instrument such as a spectrophotometer. Methods and instruments for visualizing color changes are well known in the art.

Definitions

“Nucleic Acids” as used herein means oligomers of DNA or RNA. Nucleic acids may also include analogs of DNA or RNA having modifications to either the bases or the backbone. For example, nucleic acid, as used herein, includes the use of peptide nucleic acids (PNA). The term “nucleic acids” also includes chimeric molecules.

The term “sticky end” refers to a nucleic acid sequence that is available to hybridize with a complementary nucleic acid sequence. The secondary structure of the “sticky end” is such that the sticky end is available to hybridize with a complementary nucleic acid under the appropriate reaction conditions without undergoing a conformational change. Typically the sticky end is a single stranded nucleic acid.

“Monomers” are individual nucleic acid oligomers. Typically, at least two monomers are used in hybridization chain reactions, although three, four, five, six or more monomers may be used. In some embodiments more than two monomers are utilized, such as in the HCR systems displaying quadratic and exponential growth discussed below. Typically each monomer comprises at least one region that is complementary to at least one other monomer being used for the HCR reaction.

A first monomer in a monomer pair preferably comprises an initiator complement region that is complementary to a portion of an initiator molecule. The initiator complement region is preferably a sticky end. Binding of the initiator to the initiator complement region begins an HCR reaction.

In addition, the second monomer preferably comprises a propagation region that is able to hybridize to the initiator complement region of another monomer, preferably another copy of the first monomer, to continue the HCR reaction begun by the initiator. The propagation region may be, for example, the loop region of a hairpin monomer as described below. In one embodiment the propagation region on the second monomer is identical to the portion of the initiator that is complementary to the initiator complement region of the first monomer.

The propagation region on the second monomer is preferably only available to interact with the initiator complement region of the first monomer when an HCR reaction has been started by the initiator. That is, the propagation region becomes available to hybridize to the initiator complement region of another monomer when one copy of the first monomer has already hybridized to a second monomer, as discussed in more detail below.

Preferred monomers are “metastable.” That is, in the absence of an initiator they are kinetically disfavored from associating with other monomers comprising complementary regions. “HCR” monomers are monomers that are able to assemble upon exposure to an initiator nucleic acid to form a polymer.

As used herein, “polymerization” refers to the association of two or more monomers to form a polymer. The “polymer” may comprise covalent bonds, non-covalent bonds or both. For example, in some embodiments two species of monomers are able to hybridize in an alternating pattern to form a polymer comprising a nicked double helix. The polymers are also referred to herein as “HCR products.”

An “initiator” is a molecule that is able to initiate the polymerization of monomers. Preferred initiators comprise a nucleic acid region that is complementary to the initiator complement region of an HCR monomer.

Monomers

Two or more distinct species of nucleic acid monomers are preferably utilized in an HCR reaction. Each monomer species typically comprises at least one region that is complementary to a portion of another monomer species. However, the monomers are designed such that they are kinetically trapped and the system is unable to equilibrate in the absence of an initiator molecule that can disrupt the secondary structure of one of the monomers. Thus, the monomers are unable to polymerize in the absence of the initiator. Introduction of an initiator species triggers a chain reaction of alternating kinetic escapes by the two or more monomer species resulting in formation of a polymer. In the examples below, the two hairpin monomers polymerize in the presence of an initiator to form a nicked, double helix.

In a preferred embodiment, two or more monomer species are employed that have a hairpin structure. The hairpin monomers preferably comprise loops protected by long stems. In other embodiments, monomers with a different secondary structure are provided. However, the secondary structure is preferably such that the monomers are metastable under the reaction conditions in the absence of an initiator nucleic acid. In the presence of an initiator, the secondary structure of a first monomer changes such that it is able to hybridize to a sticky end of a second monomer species. This in turn leads to a change in the secondary structure of the second monomer, which is then able to hybridize to another first monomer and continue the process. In this way, once a single copy of the first monomer interacts with a single copy of the initiator, a chain reaction is produced such that the monomers are able to assemble into a polymer comprising alternating monomer species.

A number of criteria can be used to design the monomers to achieve the desired properties. These include, for example and without limitation, sequence symmetry minimization, the probability of adopting the target secondary structure at equilibrium, the average number of incorrect nucleotides at equilibrium relative to the target structure, and hybridization kinetics.

Monomers can be synthesized using standard methods, including commercially available nucleic acid synthesizers or obtained from commercial sources such as Integrated DNA Technologies (Coralville, Iowa).

In some embodiments, monomers are derivitized with a compound or molecule to increase the molecular weight of the polymer resulting from HCR. Preferably they are derivitized at a location that does not interfere with their ability to hybridize. In other embodiments monomers comprise a fluorophore or calorimetric compound that allows the resulting polymers to be visualized.

In preferred embodiments, at least two hairpin monomers are utilized as illustrated in FIG. 1A. The monomers each preferably comprise a sticky end (a and c*, respectively), a first complementary segment (b and b*, respectively), a loop segment (c and a*, respectively), and a second complementary segment (b and b*, respectively). The first and second complementary segments are also referred to as “stems” and together form a duplex region.

The first monomer (H1) preferably comprises a sticky end a that is complementary to a first nucleic acid portion a* of an initiator (I; FIG. 1B). This sticky end is referred to herein as the “initiator complement region.” The initiator may be, for example, an analyte of interest, or a nucleic acid that is able to contact the first monomer only in the presence of an analyte of interest, as discussed in more detail below.

The second monomer (H2) preferably comprises a sticky end c* that is complementary to a portion of the first monomer that becomes accessible upon initiator binding. Preferably the sticky end c* is complementary to the loop segment c of the first monomer (FIG. 1A). The loop segment c of the first monomer is preferably not available to hybridize with sticky end c* of the second monomer in the absence of initiator.

The first and second complementary segments (b and b*) in the first and second monomers are typically substantially identical. That is, the first complementary segment b of the first monomer (H1) is able to hybridize to the second complementary segment b* of the second monomer (H2).

The first complementary segment of each monomer is also able to hybridize to the second complementary segment of the same monomer to form the hairpin structure. For example, as shown in FIG. 1A, the first monomer (H1) comprises a first complementary segment b that is able to hybridize to the second complementary segment b*. In the absence of an initiator, the first and second complementary segments of each monomer are generally hybridized to form a duplex region of the metastable monomer.

Preferably, the first complementary segment b of the first monomer is also complementary to a portion b* of the initiator, such that upon hybridization of the initiator region a* to the sticky end a (the initiator complement region) of the first monomer H1, one arm of the hairpin structure is displaced. This opens the hairpin and allows binding of the first complementary segment b to the second portion b* of the initiator strand (FIG. 1B).

The loop segment c of the first monomer is also exposed by the opening of the hairpin and is able to bind to the sticky end c* of the second monomer H2, as illustrated in FIG. 1C. This opens the second monomer hairpin H2 and the second complementary segment b* of the first monomer is able to hybridize to the first complementary segment b of the second monomer H2.

This leaves the loop region a* and first complementary region b* of the second monomer H2 exposed (FIG. 1C). The sticky end a of another first monomer (H1) species is able to bind to the exposed loop region a* of the second monomer H2, thus opening the H1 hairpin and continuing the process described above. Because the loop region a of the second monomer acts as an initiator on a second H1 monomer and allows the process to continue in the absence of further initiator, it is referred to as the propagation region.

At each step, energy is gained from the hybridization of the the sticky end of the monomer. The result is a nicked, double helix polymer comprising alternating H1 and H2 fragments. This process preferably continues in a chain reaction until all of one or both of the monomer species is used up, or the reaction is stopped by some other mechanism. If desired, the nicks in the nucleic acid polymer structures that result from HCR can by ligated (for example, using T4 DNA ligase).

Because of the self-propagating nature of the reaction, each copy of the initiator species can begin the chain reaction. Further, as long as there is a fixed supply of monomers the average molecular weight of the resulting polymers is inversely related to the initiator concentration, as can be seen in FIG. 1D.

The length of the loop, stem and sticky ends of the monomers can be adjusted, for example to ensure kinetic stability in particular reaction conditions and to adjust the rate of polymerization in the presence of initiator. In one preferred embodiment the length of the sticky ends is the same as the length of the loops. In other embodiments the sticky ends are longer or shorter than the loops. However, if the loops are longer than the sticky ends, the loops preferably comprise a region that is complementary to the sticky end of a monomer.

In some preferred embodiments the length of the loops is short relative to the stems. For example, the stems may be two or three times as long as the loops.

The loop regions are preferably between about 1 and about 100 nucleotides, more preferably between about 3 and about 30 nucleotides and even more preferably between about 4 and about 7 nucleotides. In one embodiment the loops and sticky ends of a pair of hairpin monomers are about 6 nucleotides in length and the stems are about 18 nucleotides long.

Other refinements to the system stabilize the monomer hairpins to help prevent HCR in the absence of an initiator. This can be achieved, for example, via super-stable hairpin loop sequences (Nakano et al. Biochemistry 41:14281-14292 (2002)), with ostensible structural features that could further inhibit direct hybridization to the hairpin. In other embodiments hairpin loops are made to be self-complementary at their ends. This self-complementarity “pinches” the hairpin loops, making them shorter. However, if the reactive sticky ends of each monomer are complementary to the loop regions on the opposite monomer, as described above, they will have a slight propensity to close up, thereby slowing down the reaction. This feature can be utilized if a slower reaction is desired. Completely self-complementary hairpins can also be used, for example if the monomer hairpins are forming dimers with interior loops that are more easily invaded than their hairpin counterparts. FIG. 6 illustrates a self-complementary hairpin with an interior loop that is a double helix.

Reaction conditions are preferably selected such that hybridization is able to occur, both between the initiator and the sticky end of a first monomer, and between the complementary regions of the monomers themselves. The reaction temperature does not need to be changed to facilitate the hybridization chain reaction. That is, the HCR reactions are isothermic. They also do not require the presence of any enzymes.

Variations

There are many possible variations to HCR that may improve its speed, stability and ability to amplify chemical signals. The system illustrated in FIG. 1 and discussed above exhibits linear growth in response to initiator. However, increasing the rate of polymer growth can enhance the ability to detect the presence of low copy number targets, such as a single target molecule in a large test volume. For example, monomers can be designed to undergo triggered self-assembly into branched structures exhibiting quadratic growth or dendritic structures exhibiting exponential growth. The exponential growth is limited by the available space such that it decreases to cubic amplification as the volume around the initiator fills. However, if chain reactions products are able to dissociate, exponential growth can be maintained until the supply of monomers is exhausted.

In order to achieve non-linear growth, 3 or more HCR monomers can be used. In preferred embodiments at least 4 HCR monomers are used. In some embodiments, at least one monomer in a primary monomer pair incorporate a trigger nucleic acid segment that is complementary to the exposed sticky end of one of the monomers from a secondary set of HCR monomers. Upon exposure to the nucleic acid that is to be detected, the set of primary monomers undergoes HCR to form a polymer with a periodic single stranded trigger region. Thus the trigger nucleic acid is exposed, leading to a polymerization chain reaction in the secondary set of monomers. In other embodiments, both the primary and secondary set of monomers includes a trigger segment, such that exponential growth is achieved. Exemplary schemes are presented in FIGS. 2 and 3 for achieving quadratic and exponential growth, respectively.

In one embodiment, one of a first pair of monomers comprises a bulge loop. Upon polymerization, a single stranded region results from the presence of the bulge loop. The bulge loop segment is preferably complementary to the sticky end of one of a second pair of HCR monomers. Thus, upon exposure to the initiator, the first pair of monomers undergoes HCR to form a polymer with a single stranded region that acts to trigger polymerization of the second pair of monomers. FIGS. 2A-C depict such a quadratic amplification scheme. Monomers Q1 and Q2 interact with hairpin monomers H1 and H2 (FIG. 1) after initiation by IQ to form the branched polymer schematically illustrated in FIG. 2D.

Q1 and Q2 (FIG. 2a) are metastable in the absence of the initiator I_Q. I_Qbinds to Q1 and a subsequent strand displacement interaction exposes segments f, e* and b* as shown in FIG. 2B. This single-stranded region contacts sticky end f* of Q2 and a subsequent branch migration exposes segments c, b*, d* and e*. Segment d* then interacts with another copy of Q1 at sticky end d, causing the hairpin to open up such that e* can also hybridize. At the same time, the exposed c segment initiates a linear HCR reaction with hairpins H1 and H2 (not shown). The resulting branched polymer has a main chain comprising alternating Q1 and Q2 segments and H1/H2 side chains branching off at each Q2 segment.

In a further embodiment, exponential growth is achieved in response to an initiator by combining two or more pairs of monomers. For example, monomer pair Q1 and Q2 (FIG. 2) can be used in conjunction with monomers E1 and E2 (FIG. 3) to obtain exponential growth in response to an initiator. In the presence of nucleic acid segment cb*, E1 and E2 form a linear chain that includes periodic single stranded d*e* regions. By design, the initiator sequence for E1/E2 matches the periodic single stranded region produced by Q1/Q2 and vice versa. Consequently, a mixture of Q1, Q2, E1 and E2 monomers in the presence of initiator will form a structure in which each branch of the polymer is itself a branched polymer. Either initiator cb*, corresponding to the sticky end and first complementary region of E1, or d*e*, corresponding the sticky end and first complementary region of Q1, will activate the chain reaction.

While non-linear amplification systems provide enhanced sensitivity over a linear system, they may also have an increased chance for spurious initiation of HCR and a resultant increase in false-positive signals. Several methods may be used to decrease the possibility for initiation of the system in the absence of the initiator. In systems utilizing hairpin monomers, these may include helix clamping, helix elongation and loop entropy ratchets.

The quadratic and exponential growth HCR schemes illustrated in FIGS. 2 and 3 include long single-stranded regions (b* and e* respectively). These long regions could potentially function as weak initiators. Several methods are available to reduce spurious monomer polymerization in the absence of initiator for both higher order growth schemes and linear growth schemes. These include helix clamping, helix lengthening and loop entropy ratchets. In helix clamping, the single stranded regions in one or more of the monomers are truncated at each end so that the helixes that they could potentially invade in other monomers are effectively clamped at the ends by bases that are not present in the single stranded (b* and e*) regions. Experiments have shown that this can eliminate any spurious initiation. The amount of truncation that is effective to decrease or eliminate spurious initiation can be determined by routine experimentation. For example, control experiments can be performed using fluorescent gel electrophoresis time courses to monitor strand exchange between single stranded DNA and duplex DNA (e.g., strand b* invading duplex bb*) for different clamp lengths. Using spectrally distinct dyes for the initially single stranded DNA and for the two DNA species in the duplex allows independent monitoring of all species as strand exchange proceeds. These controls can provide a systematic basis for section of clamp dimensions.

The length of the helices in the linear HCR scheme illustrated in FIG. 1 contributes directly to the height of the kinetic barrier that prevents spurious polymerization between the two hairpin species. Interactions between H1 and H2 are sterically impeded by the loop size. However, the long helices (bb*) in each hairpin provide a more fundamental kinetic barrier; the length of the helices has a direct effect on the height of the kinetic barrier that impedes spurious HCR. An increase in the length of the helices will increase the initial kinetic barrier in the uninitiated system. Thus, in some embodiments utilizing hairpin monomers, for example if spurious initiation is observed, the length of the duplex region can be increased to reduce the background noise. The helix length necessary to reduce polymerization in the absence of initiator to an acceptable level can be readily determined by routine experimentation. In some embodiments helix lengthening is combined with helix clamping.

In still other embodiments utilizing hairpin monomers, loop entropy ratchets are used to reduce HCR in the absence of initiator. An initiator opens an HCR hairpin via a three-way branch migration. This reaction is reversible because the displaced strand is tethered in the proximity of the new helix. However, by increasing the length of the single-stranded loop, the entropy penalty associated with closing the loop increases. As a result, a longer loop will bias the reaction to proceed forward rather than returning to the uninitiated state. However, larger loops are more susceptible to strand invasion. To counter this effect and allow the use of larger loops, mismatches can be introduced between the loop sequences and the complementary regions of the other monomers. Again, the loop length and amount of mismatch that produces the desired reduction in non-specific HCR can be determined by the skilled artisan through routine experimentation.

Initiator

The initiator is preferably a nucleic acid molecule. The initiator comprises an initiator region that is complementary to a portion of an HCR monomer, preferably a portion of the monomer that is available for hybridization with the initiator while the monomer is in its kinetically stable state. The initiator also preferably comprises a sequence that is complementary to a portion of the monomer adjacent to the sticky end such that hybridization of the initiator to the sticky end causes a conformational change in the monomer and begins the HCR chain reaction. For example, the initiator may comprise a region that is complementary to the first complementary region of the HCR monomer, as described above.

In the preferred embodiments, the sequence of the initiator is complementary the sticky end (initiator complementary region) and first complementary region of a first monomer. As described above, in some embodiments this will also influence the sequence of the second complementary region and the loop of the second monomer species.

In some embodiments the initiator is a nucleic acid that is to be detected in a sample or a portion of a nucleic acid that is to be detected. In this case, the sequence of the target nucleic acid is taken into consideration in designing the HCR monomers. For example, the initiator complement region, preferably a sticky end, of one monomer is designed to be complementary to a portion of the target nucleic acid sequence. Similarly, a region adjacent to the sticky end of the same monomer can be designed to be complementary to a second region of the target sequence as well. Because the second monomer will hybridize to the first monomer, the sequence of the second monomer will also reflect at least a portion of the sequence of the target nucleic acid.

In other embodiments, the initiator comprises at least a portion of a nucleic acid that is part of a “initiation trigger” such that the initiator is made available when a predetermined physical event occurs. In the preferred embodiments that predetermined event is the presence of an analyte of interest. However, in other embodiments the predetermined event may be any physical process that exposes the initiator. For example, and without limitation, the initiator may be exposed as a result of a change in temperature, pH, the magnetic field, or conductivity. In each of these embodiments the initiator is preferably associated with a molecule that is responsive to the physical process. Thus, the initiator and the associated molecule together form the initiation trigger. For example, the initiator may be associated with a molecule that undergoes a conformational change in response to the physical process. The conformational change would expose the initiator and thereby stimulate polymerization of the HCR monomers. In other embodiments, however, the initiation trigger comprises a single nucleic acid. The initiator region of the nucleic acid is made available in response to a physical change. For example, the conformation of the initiation trigger may change in response to pH to expose the initiator region.

The structure of the trigger is preferably such that when the analyte of interest is not present (or the other physical event has not occurred), the initiator is not available to hybridize with the sticky end of a monomer. Analyte frees the initiator such that it can interact with a metastable monomer, triggering the HCR polymerization reactions described above. In some embodiments analyte causes a conformational change in the trigger that allows the initiator to interact with the monomer.

The initiator may be part of a trigger comprising a nucleic acid that is linked to or associated with a recognition molecule, such as an aptamer, that is capable of interacting with an analyte of interest. The trigger is designed such that when the analyte of interest interacts with the recognition molecule, the initiator is able to stimulate HCR. Preferably, the recognition molecule is one that is capable of binding the analyte of interest.

Recognition molecules include, without limitation, polypeptides, such as antibodies and antibody fragments, nucleic acids, such as aptamers, and small molecules. The use of an initiator bound to an aptamer is described in more detail below.

In some particular embodiments, amplification of diverse recognition events is achieved by coupling HCR to nucleic acid aptamer triggers. An aptamer is identified that is able to specifically bind an analyte of interest. The analyte is not limited to a nucleic acid but may be, for example, a polypeptide or small molecule. The aptamer is linked to a nucleic acid comprising an initiator region in such a way that the initiator is unavailable to stimulate HCR in the absence of analyte binding to the aptamer.

Preferably, conformational changes in the aptamer secondary structure expose the initiator segment. In one embodiment, such an aptamer trigger is a hairpin nucleic acid that comprises an initiator segment that is complementary to the initiator complement region or sticky end of an HCR monomer. The aptamer trigger also comprises a complementary region that is complementary to a region of the HCR monomer adjacent to the sticky end, a loop region and an aptamer sequence. The hairpin aptamer trigger may also comprise a region that enhances the stability of the hairpin in the absence of aptamer binding to the analyte, such as a nucleic acid region in one arm of the hairpin that is complementary to a region of the other arm.

FIG. 5A depicts a scheme for HCR amplification of ATP binding using an aptamer construct that exposes an initiator strand upon ATP binding. The sticky end can act as a trigger for the HCR mechanism of FIG. 1 by opening hairpin H2. The region x is introduced to help stabilize the trigger in the absence of analyte. The region b* includes both the hairpin loop and the portion of the stem complementary to x. This trigger mechanism is based on conformational changes in the aptamer secondary structure (Yingfu Li (2003) Journal of the American Chemical Society 125:4771-4778) that make the initiator strand available to stimulate HCR. FIG. 5B illustrates successful detection of ATP, as well as specificity in differentiating ATP from GTP, as discussed in more detail in the Examples below.

Colorimetric HCR

The products of HCR are preferably detected using a colorimetric system based on the change in color of nano-gold particles upon aggregation. Nanometer-scale gold particles (nano-gold particles) are particles of gold having an approximate mean diameter of about 1 to about 250 nm, more preferably about 1 to about 100 nm, still more preferably about 10 to about 50 nm, and even more preferably about 15 to about 30 nm. Nano-gold particles undergo a color change based on the distance between particles. In particular, upon aggregation nano-gold particles undergo a color shift from red to blue.

Nano-gold particles can be directly associated with one or more HCR components prior to polymerization, such that upon polymerization in the presence of a target analyte, the nano-gold particles are brought into proximity with each other and change color. The gold particles can be associated with HCR components such as hairpin monomers H1, H2, Q1, Q2, E1 and E2 or even, in some embodiments, to an initiator trigger. In some preferred embodiments nano-gold particles are conjugated directly to hairpin monomers, more preferably H1, H2, Q1 and/or Q2 monomers. In other embodiments they are attached to one or more of the hairpin monomers through a linker. Preferably they are attached such that upon aggregation the spacing of gold nano-particles is less than about 100 bp, more preferably less than about 60 bp, still more preferably less than about 25 bp.

While in some embodiments nano-gold particles are attached to an HCR component prior to polymerization, such as the H1 and/or H2 monomers, in other embodiments they are part of a detection component that is able to associate with an HCR product after polymerization. Thus, in some embodiments the detection component comprises nano-gold particles that are conjugated to one or more oligonucleotides. The oligonucleotides are able to bind to HCR products, but under typical reaction conditions are not able to bind to HCR components prior to polymerization.

In preferred embodiments the detection component comprises one or more oligonucleotides that are complementary to a portion of one or more HCR monomers that is protected prior to polymerization. Reaction conditions are controlled such that the oligonucleotides (with conjugated nano-gold particles) are able to bind to the HCR polymer that is exposed upon polymerization in the presence of a target analyte. Such reaction conditions can be readily established by the skilled artisan based on particular circumstances without undue experimentation.

Oligonucleotides (and HCR components) are preferably designed such that detection component binding causes nanogold particle aggregation, preferably with a spacing of gold nano-particles of less than about 100 bp, more preferably less than about 60 bp, still more preferably less than about 25 bp.

In a detection component, the nanogold particles are preferably conjugated to two or more oligonucleotides. In some embodiments the two or more oligonucleotides are complementary to the same portion of an HCR polymer, while in other embodiments the two or more oligonucleotides are complementary to different regions of an HCR polymer.

In other embodiments a detection component is used comprising nano-gold particles conjugated to a component that interacts with the HCR polymers in other ways. For example, nano-gold particles can be conjugated to one or more oligonucleotides that are able to form triple helices with the HCR polymers. In other embodiments nano-gold particles are conjugated to aptamers that are able to bind to HCR polymers, but not the unreacted HCR components. Additionally, gold particles can be bound to small molecules (e.g., polyamides based on distamycin and netropsin), proteins, or peptides that specifically bind to the polymer structure but not to unpolymerized HCR components. Again, in preferred embodiments the spacing of nano-gold particles upon binding to HCR polymers is less than about 100 bp, more preferably less than about 50 bp and still more preferably less than about 25 base pairs.

Gold particles can be functionalized by known methods, including, for example, by coupling through a sulfur-gold bond. Gold particles also can be functionalized with a coupling reagent to allow for conjugation to other functional groups. Functionalized nano-gold particles can be coupled to a nucleic acid. In some embodiments nano-gold particles are coupled directly or through a linker to one or more HCR components. Fro example, as discussed above nano-gold particles can be conjugated to an oligonucleotide that is complementary to a portion of an HCR monomer and/or polymer.

The gold particles are most easily attached to the 5′ or 3′ ends of an oligonucleotide. However, the gold particles also can be attached to linkers extending from the nucleobases or from the backbone of a nucleic acid, using standard nucleic acid chemistry techniques. Methods of coupling to other molecules, such as peptides, are known to the skilled artisan.

The stoichiometry of coupling of nucleic acids (or other molecules) to the nano-gold particles can be varied depending upon the particular circumstances. Particles can be generated that have a single oligonucleotide conjugated (on average) or multiple oligonucleotides conjugated. In a preferred embodiment at least 2, more preferably at least 5, still more preferably at least 10, yet more preferably at least 50 and even more preferably at least 100 oligonucleotides are conjugated, on average, to each nano-gold particle.

When nano-gold particles are attached to HCR components directly or through a linker (prior to polymerization), HCR reactions are carried out generally as described above. However, when nano-gold particles are attached to a detection nucleotide (or other molecule or compound) to form a detection component that interacts with the polymerized HCR product, the detection component can be included in the reaction mixture initially, or the detection component can added during or subsequent to completion of the HCR polymerization reaction. In some preferred embodiments, the detection component is added to the reaction mixture at essentially the same time as the other HCR components.

In the presence of an analyte of interest, polymerized HCR products form, nano-gold particles aggregate and a color change can be observed. The color change may be observable by the naked eye. In other embodiments, the color change is observed by a chromatographic technique, such as thin layer chromatograph (TLC). In still other embodiments an instrument, such as a spectrophotometer, is used to detect color change in an HCR sample.

Nano-Gold HCR

In the simplest embodiment, HCR requires two hairpin nucleic acid molecules, H1 and H2 as shown in FIG. 1. Either H1, H2 or both can be labeled with a nanometer-scale gold particle. In the presence of an analyte of interest, the assembly of the H1 and H2 nucleic acids results in an extended structure that will bring the gold particles into closer proximity. The gold particles can be generated with only one oligonucleotide per particle (on average), or multiple oligonucleotides per particle. In more complex HCR systems, one or more of the other repeating units of the HCR chain can be labeled with the gold particle.

Gold functionalized with multiple oligonucleotides can be cross-linked by HCR products, as illustrated in FIG. 7A. In the example shown in FIG. 7A, the oligonucleotides linked to the gold particles are complementary to regions of the assemblies (polymers) formed in the HCR reaction and triggered by the presence of an analyte of interest. Alternatively, the components themselves (H1, H2 etc . . . ) can be labeled with nano-gold as discussed above. The proximity of the nano-gold particles changes upon polymerization in the presence of the analyte, leading to a color change.

Applications

Colorimetric HCR may be used to produce a visual signal indicating the presence of a target molecule. HCR can be initiated by the presence of a target molecule comprising an initiator nucleic acid region. In other embodiments HCR is initiated by any event that exposes an initiator nucleic acid strand (for example, an aptamer binding to its target ligand so as to expose an initiator strand, as discussed above). In both cases, hybridization of the initiator strand to the initiator complementary region on an HCR monomer triggers polymerization of the HCR monomers. In the case where nano-gold particles have been incorporated in an HCR component, such as in one or more of the monomers themselves, the polymerization event causes aggregation of the nano-gold particles, leading to a color change from red to blue. In other embodiments, binding of multiple detection components comprising nano-gold particles to the HCR polymers leads to aggregation and a color change from red to blue. For some amplification applications in which detection is the primary objective, HCR may serve as an attractive alternative to PCR (polymerase chain reaction).

Colorimetric HCR can be used to detect a physical change in a sample. For example, as discussed above an initiator trigger may be used to trigger polymerization of two or more HCR monomers in response to a physical change in the sample. This may be, for example, and without limitation, a change in pH, temperature, magnetic field or conductivity in the sample. By using calorimetric HCR with nano-gold as an indicator, a simple color change in a sample can provide an easy way to identify environmental conditions and/or changes.

In other embodiments calorimetric HCR is used to identify a physical characteristic of a sample. An initiator trigger may be used that is activated only when the sample has a particular characteristic, such as a particular pH, temperature or conductivity. In one embodiment an initiator trigger is utilized that exposes the initiator and triggers HCR only when the pH is above a predetermined level, leading to a color change that is easily observed. The presence of such products indicates a pH above the predetermined level.

Colorimetric HCR may be used to construct a biosensor. In one embodiment the sensor would comprise two or more HCR monomers and would detect the presence of initiator in a sample (or particular environmental conditions, as discussed above). Whenever initiator is present, HCR will occur, resulting in the creation of a polymer from the individual monomer species and a readily detectable color change.

Colorimetric HCR can be used to identify the presence of nucleic acids, polypeptides or other molecules of interest in a sample. For example, nucleic acids associated with a pathogen can be identified in a biological sample obtained from a patient. In some embodiments, a sample is obtained from a patient and tested for the presence of nucleic acids associated with a virus, such as HIV. One or more pairs of HCR monomers are contacted with the sample, where at least one of the monomers comprises an initiator complementary region that is complementary to a portion of the nucleic acid to be detected. An easily observed color change indicates the presence of the virus. Thus, calorimetric HCR provides an inexpensive, fast and reliable method of diagnosing diseases, disorders or conditions in a patient.

Colorimetric HCR can also be used to determine analyte concentration. In some embodiments, the concentration of analyte is determined by comparing the color change in a particular sample with the color change observed from HCR reactions in one or more control samples with a known concentration of the analyte. In this way the concentration of analyte in the unknown samples can be determined to be the same as one of the control samples, greater than one of the control samples, less than one of the control samples, or in the range of concentration between two control samples. Thus, the number of control reactions can be adjusted based on the particular circumstances to provide more or less sensitive determination of analyte concentration. For example, if a relatively exact analyte concentration is necessary, the number of control samples can be increased. On the other hand, if only a broad idea of analyte concentration is necessary, fewer control samples can be used.

Controls reactions are preferably carried out under similar conditions to the HCR reaction in which a concentration is to be determined. In some embodiments control HCR reactions are carried out at approximately the same time as the HCR reaction of interest. In other embodiments, control HCR reactions are carried out under controlled conditions, for example at room temperature. The controlled conditions may approximate those in which the HCR reactions of interest are anticipated to be carried out.

For some applications, it may be useful to employ colorimetric HCR for both amplification and capture of a target. Thus, the HCR mechanism can be designed to capture a target molecule, leaving the target tethered to the resulting polymer. The capture of the target is signaled by the color change of the sample. The separation step is facilitated by the increased size of the HCR product with respect to the analyte of interest. Thus, even small, rare nucleic acid targets can be readily isolated from a sample. In one embodiment the positive HCR reactions are run on a gel under conditions that do not disrupt binding between the target and the HCR monomer. The HCR products are then isolated from the gel and the target is purified.

More sophisticated biosensors can be created by the incorporation of DNA or RNA aptamers or other mechanisms that expose HCR initiator strands only in the presence of a particular analyte of interest or a particular physical change in the system. FIG. 5A shows how ATP can be used to trigger HCR. FIG. 5B shows illustrative results demonstrating sensitivity to initiator concentration and specificity in detecting ATP relative to GTP.

Thus in some embodiments an initiator region is linked to a recognition molecule that is specific for an analyte to be detected in a sample to form an initiator trigger. The initiator is only made available to stimulate HCR upon analyte binding to the recognition molecule. Preferably, the recognition molecule is an aptamer that is specific for an analyte of interest, such as a polypeptide associated with a disease or disorder. The polypeptide may be, for example, a cancer antigen or a polypeptide associated with a pathogen or infectious agent.

In one embodiment a biological sample, such as blood, urine, cerebrospinal fluid, or tissue, is obtained from a patient suspected of suffering from a disease or disorder, or of having a particular condition, such as being pregnant. The sample is incubated with one or more pairs of HCR monomers and an initiator trigger molecule comprising an initiator and an aptamer specific for a polypeptide or other molecule associated with the disease, disorder or condition. In some embodiments one or more of the HCR monomers comprise nano-gold particles. In other embodiments, a detection component comprising nano-gold is also added to the reaction. A simple color change in the sample from red to blue indicates that the analyte associated with the disease, disorder or condition is present in the sample. One or more control reactions can also be run simultaneously.

EXAMPLES

HCR monomers comprising DNA sequences were designed using a combination of criteria (Dirks et al. Nucleic Acids Research 32:1392-1403 (2004)). These included sequence symmetry minimization (Seeman N. C. J. Theor. Biol. 99:237-247 (1982)), the probability of adopting the target secondary structure at equilibrium (Hofacker et al. Monatsh. Chem. 125:167-188 (1994)), the average number of incorrect nucleotides at equilibrium relative to the target structure (Dirks et al. Nucleic Acids Research 32:1392-1403 (2004)) and hybridization kinetics (Flamm et al. RNA 6:325-338 (2000)). The sequences of the monomers and initiator for the basic HCR system illustrated in FIG. 1 and the aptamer trigger HCR system illustrated in FIG. 5 are shown in Table 1. The aptamer system included new sequences to ensure compatibility with the fixed sequence of the aptamer. DNA was synthesized and purified by Integrated DNA Technologies (Coralville, Iowa).

TABLE 1SystemStrandSequence*BasicH15′-TTA ACC CAC GCC GAA(SEQ ID NO:1)TCC TAG ACT CAA AGTAGT CTA GGA TTC GGCGTG-3′H25′-AGT CTA GGA TTC GGC(SEQ ID NO:2)GTG GGT TAA CAC GCCGAA TCC TAG ACT ACTTTG-3′I5′-AGT CTA GGA TTC GGC(SEQ ID NO:3)GTG GGT TAA-3′Aptamer†H15′-CAT CTC GGT TTG GCT(SEQ ID NO:4)TTC TTG TTA CCC AGGTAA CAA GAA AGC CAAACC-3′H25′-TAA CAA GAA AGC CAA(SEQ ID NO:5)ACC GAG ATG GGT TTGGCT TTC TTG TTA CCTGGG-3′I^ATP5′-CCC AGG TAA CAA GAA(SEQ ID NO:6)AGC CAA ACC TCT TGT custom character

I5′-CCC AGG TAA CAA(SEQ ID NO:7)GAA AGC CAA ACC-3′
*In the hairpin sequences, loops are in bold and sticky ends are italicized.

†Aptamer nucleotides are italicized and bolded.

For the basic HCR system illustrated in FIG. 1, concentrated DNA stock solutions were prepared in buffer that was later diluted to reaction conditions. The buffer comprised 50 mM Na2HPO4/0.5M NaCl (pH 6.8).

Monomers H1 and H2 (FIG. 1B) were mixed at various concentrations in the presence and absence of initiator. Stock solutions of I, H1 and H2 were diluted in reaction buffer to three times their final concentration and 9 μl of each species was combined, in that order to give a 27 μl reaction volume. Six different concentrations of initiator were used (0.00, 10.00, 3.20, 1.00, 0.32 and 0.10 μM) in a 1 μM mixture of H1 and H2. Reactions were incubated at room temperature for 24 hours before running 24 μl of each product on a gel. Samples were loaded on 1% agarose gels containing 0.5 μg EtBr per ml of gel volume. The gels were prepared using 1×SB buffer (10 mM NaOH, pH adjusted to 8.5 with boric acid). The agarose gels were run at 150 V for 60 minutes and visualized under UV light.

FIG. 1D illustrates the results of the HCR reactions and the effect of initiator concentration on amplification. Lanes 2-7 of the gel shown in FIG. 1D are the results of the HCR reactions at the various initiator concentrations, respectively. Lanes 1 and 8 are DNA markers with 100-bp and 500-bp increments respectively. As illustrated by FIG. 1D, introduction of an initiator strand triggers a chain reaction of hybridization that results in the production of polymers of various sizes. The average molecular weight of the polymers is inversely related to the initiator concentration (FIG. 1(d)). The inverse relationship follows from the fixed supply of monomer hairpins, but the phenomenon was observed after 10 minutes, when the supply of monomers had not been exhausted.

These results confirmed an earlier experiment in which 1 μM of H1 and H2 were reacted overnight in 0.5M NaCl, 50 mM Na₂HPO₄at pH 6.5 with initiator at concentrations of 0, 1, 0.1, 0.01, 0.001 and 0.0001 μM. With no initiator HCR reactions were not observed. In addition, no visible polymer growth was observed at initiator concentrations of 0.001 and 0.0001 μM. At the other initiator concentrations an inverse relationship was observed between the initiator concentration and the average molecular weight of the resulting polymers.

In another set of experiments, the aptamer trigger illustrated in FIG. 5A was utilized. The aptamer trigger (I^ATP) comprised an initiator region corresponding to the initiator used in the experiments described above, linked to an aptamer that is able to specifically interact with ATP (Huizenga et al. Biochemistry 34:656-665 (1995)). In addition, the aptamer trigger comprises a stabilizing region designed to stabilize the trigger in the absence of ATP. The aptamer trigger is designed such that in the presence of ATP the hairpin is opened and the initiator region exposed, thereby triggering polymerization of the H1 and H2 monomers. The sequence of I^ATPis provided in Table 1, above.

Reactions were carried out with various combinations of H1, H2, I, I^ATP, ATP and GTP. Concentrated stock solutions of the constituents were diluted to reaction conditions: 5 mM MgCl2/0.3 M NaCl/20 mM Tris (pH 7.6). Reactions were performed with 1.4 mM ATP and/or GTP. DNA species were combined to yield 1 μM concentrations in 27 μl of reaction buffer, with additions made in the following order: buffer and/or initiator I or aptamer trigger I^ATP, H1, and then H2 (I and I^ATPinteract with H2 rather than H1). In this case, 1 μl of 40 mM ATP, 40 mM GTP or water was added to each reaction, as appropriate, for a total reaction volume of 28 μl.

Reactions were incubated at room temperature for one hour and run on agarose gels (as described above) or native polyacrylamide gels. Native polyacrylamide gels were 10% precast gels made with 1×TBE buffer (90 mM Tris, 89 mM boric acid, 2.0 mM EDTA, pH 8.0). The polyacrylamide gels were run at 150V for 40 minutes in 1×TBE and stained for 30 minutes in a solution containing 5 μg EtBr per ml.

FIG. 5B shows a representative agarose gel illustrating that the aptamer trigger I^ATPcan initiate polymerization of H1 and H2 in the presence of ATP and that ATP can be distinguished from GTP. Hairpins H1 and H2 did not polymerize when mixed in the absence of initiator (H1+H2; Lane 1), but did polymerize when the initiator I was added (H1+H2+I; Lane 2). ATP alone was unable to trigger the polymerization of the hairpin monomers (H1+H2+ATP; Lane 3) and no polymers were observed from the combination of aptamer trigger with ATP in the absence of hairpin monomers (IATP+ATP; Lane 4). Some weak spurious HCR was observed in the absence of ATP from the combination of monomers and aptamer trigger (H1+H2+I^ATP; Lanes 5) or in the presence of GTP (H1+H2+I^ATP+GTP; Lane 7), respectively. Strong HCR amplification of ATP recognition was seen when the monomers were combined with the aptamer trigger in the presence of ATP (H1+H2+I^ATP+ATP; Lane 6). A DNA ladder is shown in Lane 8 (100-1000 bp in 100 bp increments).

The kinetics of HCR reactions were explored using fluorescence quenching. The adenine analog 2-aminopurine (2AP) fluoresces when single stranded but is significantly quenched when in a stacked double-helical conformation (Rachofsky et al. Biochemistry 40: 996-956 (2001)). Monomer usage was monitored as polymerization occurred by replacing H1 with the labeled hairpin H1^2AP. H1^2APwas prepared by substituting 2AP for the third base (A) in the sticky end of H1 (see Table 1). Monitoring 2AP fluorescence was used rather than standard end-labeled strands because the local environment of quenched 2AP was the same regardless of whether initiator (I) or monomer (H2) performs the quenching.

Fluorescence data were obtained using a fluorometer from Photon Technology International (Lawrenceville, N.J.), with the temperature controller set to 22° C. Excitation and emission wavelengths were 303 and 365 nm, respectively, with 4 nm bandwidths. Stock solutions of 0.40 μM H12AP and 0.48 μM H2 were prepared in reaction buffer as described above, heated to 90° C. for 90 seconds and allowed to cool to room temperature for 1 hour before use. For each experiment, 250 μl of H12AP was added to either 250 μl of H2 or 250 μl of reaction buffer. These 0.20 μM H12AP solutions were allowed to sit at room temperature for at least 24 hours before fluorescence measurements were taken. The initial signal was obtained after rapidly pipetting the sample in the cuvette to obtain a stable fluorescence baseline. After acquiring at least 2,000 seconds of the baseline, runs were paused for about 1 minute to add 20 μl of initiator (either 20 μM or 2.5 μM) and allow mixing by rapid pipetting. The final reaction volume was 520 μl for all experiments. The variation in initial fluorescence intensities was about 10% across three experiments.

As evidenced by the results presented in FIG. 1E the hairpin monomers H1 and H2 do not hybridize in the absence of initiator. Addition of initiator (I) to the hairpin mixture led to fluorescence quenching via HCR (bottom band from 0 to 2000 seconds, then dropping to middle band from 2000 seconds on)

The same quenched baseline was achieved without HCR by combining H1^2APwith excess initiator in the absence of H2 (FIG. 1(E), middle band from 0 to 2000 seconds, then dropping to bottom band from 2000 seconds on). In this case, each initiator molecule caused one fluorescent signaling event by binding to H1^2AP. With H2 present, HCR performed fluorescent amplification, allowing each initiator molecule to alter the fluorescence of multiple hairpins.

Addition of insufficient initiator to H1^2APprovided only partial quenching (FIG. 1(E), top band), demonstrating that HCR, and not initiator alone, was responsible for exhausting the supply of H1^2APmonomer.

Colorimetric HCR

Colorimetric HCR reactions were run for 3.5 hours using 96 nM DNA hairpins, 0.1×DNA target and 4 nM gold conjugates at room temperature. Nanogold particles were conjugated to an oligonucleotide complementary to a portion of the DNA hairpins that is protected in the absence of HCR polymerization, but able to bind to HCR polymers produced in the presence of a target analyte. In this case, a DNA target molecule was used. In a TLC spot test, a negative control lacking the DNA target showed a red spot, while the sample with the DNA target showed a blue spot, consistent with the expected color change in the nanogold particles from clustering associated with binding to HCR polymers.

Although the foregoing invention has been described in terms of certain preferred embodiments, other embodiments will be apparent to those of ordinary skill in the art. Additionally, other combinations, omissions, substitutions and modification will be apparent to the skilled artisan, in view of the disclosure herein. Accordingly, the present invention is not intended to be limited by the recitation of the preferred embodiments, but is instead to be defined by reference to the appended claims. All references cited herein are incorporated by reference in their entirety.

Colorimetric readout of hybridization chain reaction

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