- Preliminary communication
- Open Access
Beyond allostery: Catalytic regulation of a deoxyribozyme through an entropy-driven DNA amplifier
© Eckhoff et al; licensee BioMed Central Ltd. 2010
- Received: 10 June 2010
- Accepted: 1 October 2010
- Published: 1 October 2010
The programmability and replicability of RNA and DNA have respectively enabled the design and selection of a number of allosteric ribozymes and deoxyribozymes. These catalysts have been adapted to function as signal transducers in biosensors and biochemical reaction networks both in vitro and in vivo. However, allosteric control of nucleic acid catalysts is currently limited by the fact that one molecule of effector (input) generally regulates at most one molecule of ribozyme or deoxyribozyme (output). In consequence, allosteric control is usually inefficient when the concentration of input molecules is low. In contrast, catalytic regulation of protein enzymes, as in protein phosphorylation cascades, generally allows one input molecule (e.g., one kinase molecule) to regulate multiple output molecules (e.g., kinase substrates). Achieving such catalytic signal amplification would also be of great utility for nucleic acid circuits. Here we show that allosteric regulation of nucleic acid enzymes can be coupled to signal amplification in an entropy-driven DNA circuit. In this circuit, kinetically trapped DNA logic gates are triggered by a specific sequence, and upon execution generate a peroxidase deoxyribozyme that converts a colorless substrate (ABTS) into a green product (ABTS•+). This scheme provides a new paradigm for the design of enzyme-free biosensors for point-of-care diagnostics.
- Branch Migration
- Input Molecule
- Allosteric Control
A variety of functional nucleic acids have been engineered over the past two decades, including not only simple binding elements (aptamers [1, 2]) and catalysts (ribozymes  and deoxyribozymes ), but also more 'intelligent' molecular parts, such as aptamer beacons and allosteric ribozymes that can sense biomolecules [5, 6], process molecular information [7, 8], and regulate biochemical systems . However, most regulatory nucleic acid elements are based on allosteric control, which has a fundamental limitation: one input molecule generally yields only one output molecule. Such stoichiometric or sub-stoichiometric regulation is often insufficient for effective metabolic regulation or diagnostic signal transduction, especially when the concentrations of input molecules are low.
In contrast, natural catalytic cascades, such as the phosphorylation of proteins by kinases, readily amplify low input signals. Although in principle ribozymes and deoxyribozymes could participate in similar cascades as catalysts [10–12], no generalizable method for implementing such cascades has yet been established. On the other hand, DNA and RNA can catalyze chemical reactions not only by forming intricate tertiary structures, but also by simply forming Watson-Crick base pairs. In fact, by serving as a hybridization template, DNA can control and catalyze a wide range of chemical reactions , some of which can yield products capable of regulating downstream reactions. More recently, Zhang and coworkers have designed a scheme for highly efficient, enzyme-free, entropy-driven catalytic reactions that relies only on the dynamic hybridization of DNA strands [14–17]. Because of its chemical simplicity, this scheme is expected to allow the development of enzyme-free DNA circuits substantially more complex and robust  than previous enzyme-dependent examples [19–22]. Similar strand displacement-based schemes using DNA hairpins as substrates have also been devised [23, 24]. Moreover, it has been shown that the principles used to construct aptamer beacons and allosteric ribozymes  can also be applied to these schemes in order to create DNA circuits that use molecules other than nucleic acids as input signals .
While DNA circuits may prove useful as diagnostics, strand-exchange reactions have so far been monitored by sophisticated analytical devices. As an example of the possibilities available for signal transduction, we convert one molecule of input DNA to multiple molecules of a peroxidase deoxyribozyme [12, 25] that in turn converts the colorless substrate 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid) (ABTS) into the readily observed green product ABTS•+. We also demonstrate that an entropy-driven catalytic DNA circuit can function as a generic signal amplification module that allows lower concentrations of input molecules to control the production of higher concentrations of deoxyribozymes, and thus exceed the limit of stoichiometric allosteric control. The system is qualitatively sensitive to mismatches in the input nucleic acid, suggesting that the combined entropy-driven strand exchange and allosteric deoxyribozyme circuit might facilitate the future development of enzyme-free, point-of-care diagnostic assay system [26–28].
Sequence of DNA sub-domains used in this work
In this circuit, the amplification module contains a Gate duplex at 100 to 200 nM, and a Fuel strand at a higher concentration (300 nM to 1 μM); this will allow the entropy-driven execution of the circuit. The Gate duplex in turn consists of a Dock strand and an Invader strand. Although in principle the Fuel can displace the Invader from the Gate, this reaction is very slow due to the stability of DNA duplex. However, in the presence of even low concentrations of an input (the Trigger strand), the sub-domain 1t at the 3' end of the Trigger can bind the toehold sub-domain 1t* at the 5' end of the Dock, and initiate a branch migration reaction in which the Trigger displaces the Invader from the Dock. After the Invader dissociates, a Fuel strand can interact with the Dock via the sub-domain 2t at its 5' end, and initiate a backward branch migration to displace, and thus recycle, the Trigger (with the concomitant formation of the Waste_1 duplex). The recycled Trigger can then catalyze another cycle of exchange between the Invader and the Fuel on the Dock. Thus, the net reaction of these two processes is the reversible reaction Gate + Fuel = Invader + Waste_1, where the Trigger serves as a catalyst to accelerate this otherwise very slow reaction, and thereby reach an equilibrium where a substantial amount of Invader is released.
The product of the amplification module, namely the Invader strand, can then enter the allosteric deoxyribozyme module (Figure 1B) which consists solely of a Reporter duplex. The reporter duplex is formed by the hybridization of the DNAzyme strand and the Blocker strand. The DNAzyme strand has a catalytic domain 3 (colored dark purple in Figure 1B) that can fold into a G-quadruplex and exhibit peroxidase activity in the presence of hemin. However, the activity of the deoxyribozyme is inhibited by hybridization to the Blocker strand in the Reporter duplex. The Invader strand produced by the amplification module can displace the DNAzyme from the Reporter duplex with the concomitant formation of the Waste_2 duplex. Only upon Invader-mediated displacement can the DNAzyme strand undergo a conformational change and fold into an active G-quadruplex conformation and (in the presence of hemin and H2O2) oxidize the colorless substrate ABTS to produce the readily observed green product ABTS•+. Thus, the overall function of the combined circuit is to amplify one molecule of Trigger into multiple molecules of G-quadruplex deoxyribozyme and colored product.
Figure 2D directly compares the extent of reaction between different samples after 1 hr. Notably, the increase of fluorescent signal by 5 nM Trigger in the presence of Fuel was ~0.3 RFU (comparing samples #3 and #4), which corresponded to the production of ~20 nM of Invader. Thus, in the context of the circuit as a whole 5 nM Trigger presumably produced 20 nM Invader, and thus the original signal was amplified by (20 nM/5 nM =) 4-fold within an hour. While this value is relatively small compared to other methods, it should be noted that the extent of amplification was primarily limited by the high, uncatalyzed background reaction which in 1 hr produced a signal equivalent to that produced by ~25 nM Invader. This background can be tuned by increasing the purity of the Gate duplex (see Section 2 of [Additional file 1]), and by 'clamping' and 'padding' the duplex to decrease non-specific strand exchange .
The combined chemical system could thus be assayed for the ability to detect input Trigger strands. Notably, in the presence of Gate and Fuel, as little as 25 nM of Trigger was able to produce sufficient peroxidase activity for visual observation of ABTS•+ formation after only 15 min of reaction (Figure 3, sample #6). Observed peroxidase activity further increased when the Trigger concentration was increased to 50 nM (Figure 3, samples #7~9). The circuit could be shown to be dependent upon both Trigger and Fuel. In the absence of Fuel, 50 nM of Trigger alone did not yield sufficient peroxidase activity for visual observation (Figure 3, sample #13). In the absence of Trigger, 200 nM of Gate only restored a small fraction of peroxidase activity even with the presence of 500 nM of Fuel (Figure 3, sample #2 and #3). As a positive control, the addition of 200 nM of Invader to 200 nM of Gate and 200 nM of Reporter almost completely restored peroxidase activity (Figure 3, compare sample #4 with sample #5).
Zhang and Winfree have shown that single-nucleotide mutations, insertions, and deletions in the catalyst strand can result in 10- to 300-fold reductions in its efficiency in catalyzing strand exchange . These reductions in signal observed with single-nucleotide mismatches are comparable to other well-developed DNA sensors [26–28, 31–33]. Consistent with these findings, we observed that when a single nucleotide was changed in the toehold region (Figure 3, inset), the mutant Trigger did not yield any peroxidase activity above background even at 150 nM concentration (Figure 3, sample #10~12).
In summary, by coupling an entropy-driven DNA circuit with deoxyribozyme catalysis we created a catalytic cascade akin to phosphorylation-based protein regulation in biology. Optimization of circuit design and purification methods (see Section 2 of [Additional file 1]) coupled with cascaded and autocatalytic amplification schemes [14, 24] should greatly improve circuit performance. Overall, these results suggest that entropy-driven DNA circuits coupled with colorimetric readouts could lead to new point-of-care nucleic acid detection methods, including field-based qualitative plus/minus discrimination between mutant and wild-type alleles.
We thank Dr. David Yu Zhang for helpful discussions on the design of the amplification module, and Dr. Bingling Li for her suggestions on the optimization of conditions for the colorimetric assay. This work was supported by the Welch foundation (F-1654) and National Institute of Health (GM077040-08, EB007689). XC was partly supported by the Graduate School Continuing Fellowships of the University of Texas at Austin.
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