BL21 DE3 Star cells (Invitrogen, C601003), BL21dLacGold cells (Didovyk et al., 2017) (Agilent, 230,132), or the CRISPR+, CRISPR-derivatives from this work were grown overnight at 37°C on 2xYT agar plates with the appropriate antibiotics. A single colony was grown in a 5 ml 2xYT culture overnight at 37°C. The next day, a 50 ml culture was started with a 1:1,000 dilution overnight at 37°C. On the fourth day, a total of 2 L of culture was started and split in 5 2-L Erlenmeyer, at an initial OD₆₀₀ 0.05 in 2xYT supplemented with 40 mM phosphate dibasic (Sigma, 94,046), 22 mM phosphate monobasic (Sigma, 74,092) and 20 g/L D-glucose. This culture was grown at 37°C with vigorous agitation (230 rpm) until OD₆₀₀ reached 0.6–0.8 (approximately 2.5 h) and cells were induced with 1 mM IPTG for another 3 h at 37°C before harvesting by centrifugation at 5,000 g and 4°C. Pellets were washed twice with cold S30B buffer (5 mM tris acetate pH 8.2, 14 mM magnesium acetate, 60 mM potassium glutamate, and 2 mM dithiothreitol) (Sun et al., 2013). The pellet was then weighted, and a relationship of 0.9 ml of S30B and 5 g of 0.1 mm diameter silica beads (Biospec, 11079101) were added per Gram of pellet obtained. 2.5 ml bead-beating tubes and cups were filled with the viscous solution composed of cells and glass beads, without generating bubbles, sealed and beaten for 30 s using a homogenizer (MP Biomedicals, FastPrep-24 5G). To remove the beads from extracts, processed samples were placed on the top of a micro-chromatography column (Biorad, 7326204), which was placed into an empty bead-beating tube. The bead-beaten tube attached to the micro-chromatography column and the empty recipient tube was placed into a 15 ml Falcon tube and centrifuged at 6,000 g for 5 min at 4°C. Properly beat extracts should appear clear, and two distinct layers should be observed. The supernatant from all tubes was pooled and agitated at 37°C inside a 5 ml unsealed tube for 1 hour for runoff. After the run-off reaction, the tubes were placed on ice and re-centrifuged at 6,000 g for 10 min at 4°C to pull down the debris generated during the run-off reaction. The supernatant from this centrifugation, i.e., the crude extract, was aliquoted, frozen, and stored at −80°C until use. A link to the full protocol of crude extract and cell-free reaction preparation can be found here: https://www.protocols.io/view/preparation-of-cell-free-rnapt7-reactions-kz2cx8e.

The in-house cell-free reactions were composed of 45% crude lysate and 40% reaction buffer. The remaining 15% included DNA input solution chlorophenol red-β-D-galactopyranoside (Sigma, 59,767 at final concentration of 0.6 mg/ml), and in the case of the RNA sensing reactions, trigger RNA from in vitro transcription. A typical reaction is composed of 50 mM HEPES pH 8, 1.5 mM ATP and GTP, 1.4 mM CTP and UTP as triphosphate ribonucleotides, 0.2 mg/ml tRNA (Roche, 01109541001), 0.26 mM Coenzyme A, 0.33 mM NAD, 0.756 mM cAMP, 0.0068 mM folinic acid, 0.112 mg/ml spermidine, 2% PEG-8000, 3.4 mM of each of the 20 amino acids (glutamate is also added in excess in potassium and magnesium salts), and 12 mg/ml maltodextrin and 0.6 mg/ml sodium hexametaphosphate (Sigma, 305,553) or 30 mM 3-PGA as an energy source. Cell-free reactions were mounted on ice in a final volume of 10 µL in 1.5 ml Eppendorf tubes and vortexed for 30 s before sampling 5 µL that were loaded in V-bottom 96 well plates (Corning, CLS3957) or rounded 384 well-plates (Corning, CLS3540). All the reactions were incubated at 29°C in a Synergy HTX plate reader (BioTek).

All plasmids used in this work correspond to single transcriptional units (Level 1 plasmids) that were prepared using Golden Gate assembly from Level 0 parts (T7 Promoter, T7 terminator, Toehold Sensors, Triggers, etc.) (Pollak et al., 2019). The level 0 parts were previously prepared by Gibson assembly (Gibson et al., 2009) from PCR linear DNA amplified from gblocks (IDT). All plasmids were commercially sequenced before use. Plasmid DNA input was produced by midi prepping an overnight culture of 200 ml LB with the appropriate strain (Promega, A2492) and cleaned again using PCR cleanup (Promega, A6754). Plasmid DNA inputs were used in a set of concentrations ranging from 0.5 to 10 nM. Input linear DNA was produced by PCR and cleaned with PCR cleanup kit (Promega, A6754), quantified and diluted to desired concentrations using ultra-pure water. A list of all the primers and plasmids used in this work is shown in Supplementary Tables S1, 2, respectively.

PCR products containing the trigger T7 transcriptional unit were cleaned by PCR cleanup kit (Promega, A6754) and 250 ng were processed by in vitro transcription using the HiScribe T7 kit (Promega, E2040S) and incubated at 37°C overnight. The products were then treated with DNAseI for 1 hour at 37°C and the enzyme was inactivated by heat at 70°C for 10 min. Next, standard RNA clean up steps were performed according to the RNeasy MinElute kit (Qiagen, 74,204) before quantification.

We used the NASBA lyophilized kit from Life Sciences following the manufacturer’s instructions. Negative controls and RNA dilutions in the range 27 mM to 0.2 fM were prepared in ultra-pure water just before use. The lyophilized reaction buffer containing nucleotide mix (Life Sciences, LRB-10) was reconstituted with DRB-10 diluent (Life Sciences, DRB-10), heated at 41°C for 5 min and kept at room temperature. The initial mixture, consisting of 10 µL of the reconstituted reaction buffer, 1 µL RNAsin (Promega, N2111), 380 mM of each DNA primer, 2 µL ultra-pure water and a 1 µL RNA amplicon dilution, were assembled at 4°C and incubated at 65°C for 2 min, followed by a 10 min annealing at 41°C. During annealing, the lyophilized enzyme mix, consistent of AMV RT, RNaseH, T7 RNAP, and high molecular weight sugar mix (Life Sciences, LEM-10), was reconstituted with cold D-PDG (Life Sciences, D-PDG-10) and placed on ice. Immediately after annealing, 5 µL of the dissolved enzyme mix was added to the reaction, to a final volume of 20 µL, and the mixture was incubated at 41°C for 2 h with thermocycler lid at 98°C. A 10 min incubation at 70°C was performed for enzyme inactivation. The amplified product was subsequently cleaned up with the RNeasy MinElute kit (Qiagen, 74,204).

Lyophilization was performed by assembling 9 µL of cell extracts and 8 µL of reaction buffer in a PCR tube. In a separate tube, 3 µL of the corresponding plasmid were mixed with 1 µL of substrate (9 mg/ml), when LacZ reporter was used. Tubes containing the assembled reactions were closed with adhesive aluminum film and punctured with a 16-gauge needle to create a hole. The tubes were placed in a FreeZone 2.5 L Triad Benchtop Freeze Dryer (Labconco), previously pre-chilled at −75°C (shelf temperature), for overnight freeze-drying of two segments. The first segment was at −75°C (shelf temperature) with a temperature collector of −80°C for 12 h and 0.04 mbar of pressure. The second segment was performed at −20°C for 4 h with the same pressure. Samples were stored at room temperature in open plastic bags over 30 g of silica inside a closed Tupperware. Rehydration of cell-free reactions was done with 20 µL of a plasmid solution in ultra-pure water. pT7:sfGFP was used at 6 nM or 8 nM final concentration whereas ZIKV Toehold 27 was used at 10 nM final concentration. Trigger 27 RNA was added at a final concentration of 300 nM.

With the aim of designing novel toehold sensors, we implemented an algorithm developed by Green et al. (Green et al., 2014), as an in silico tool called NupackSensors (http://www.github.com/elanibal/NupackSensors). To identify possible triggers from a target sequence, the algorithm first determines all contiguous 36 nucleotide sub-sequences. Each possible trigger defines one specific toehold sensor. After filtering out the sensors that contained stop codons, potential structural defects of each design were calculated, along with a set of thermodynamic parameters (Supplementary Figure S1; Supplementary Tables S3, 4). The following score function was implemented, and one score value was assigned to each of the possible designs (Ma et al., 2018): S c o r e = − 71 d S e n s o r − 49.1 d A c t i v e S e n s o r − 22.6 d B i n d i n g S i t e + 54.3

Here, d S e n s o r represents the average number of incorrectly paired nucleotides with respect to the ideal toehold sensor structure, defined as “.........................(((((((((((...(((((............)))))...))))))))))).....................” (Pardee et al., 2016) in dot-bracket notation (Supplementary Figure S1). Similarly, the parameter d A c t i v e S e n s o r represents the average number of incorrectly paired nucleotides with respect to the ideal activated sensor structure. d B i n d i n g S i t e represents the deviations from the perfect single-stranded binding site in the toehold domain, which is essential for the initial trigger binding and subsequent strand-displacement reaction. After assigning one score to each toehold sensor design, they are ranked.

For the PVY toehold sensor design, two RNA target sequences were evaluated in NupackSensors, corresponding to the long and short sequences found to be conserved in several PVY strains (Supplementary Tables S5, 6). For each of them, four of the highest scores were picked for experimental evaluation. Linear DNA encoding the PVY toeholds were prepared by PCR using specific primers that add the T7 promoter and each toehold sensor sequence on their 5’ tails along with the UNSXR reverse primer. LacZ full length was used as template (Supplementary Table S1 for primer sequences).

Sequences of each operon of the genes that are part of the RecBCD complex and the EndI endonuclease were identified in E.coli K12 strain genome using the web platform RegulonDB (Salgado et al., 2013). sgRNAs were designed according to (Larson et al., 2013), following these steps: all available 5'->3' PAM sites (CCN) within the nucleotide sequence of the gene of interest were marked, identifying contiguous sites as target candidates; the target candidates were analyzed and selected as the 18–22 bp contiguous to the PAM sequence that are within the first ∼156 nt of the CDS (i.e., counting from the ATG); sequences that end in C or T were selected so that the sgRNA begins with A or G (corresponding to nucleotide +1 of the sgRNA transcript) since this increases the transcription of the promoter used (Larson et al., 2013; Qi et al., 2013). The designed sgRNA corresponded to the reverse complementary sequences of the chosen target. These steps were performed in ApE open source software (https://jorgensen.biology.utah.edu/wayned/ape/). We designed three sgRNAs that targeted the cistron of recB and recD, recC and endA genes, respectively.

Linear DNA fragments of 1.5 kb and 500 bp were prepared via PCR for its use as linear DNA input and standards, respectively. Those were purified by wizard gel and PCR clean-up kit (Promega), achieving a final concentration of 200 ng/μL 600 ng of the 1.5 kb linear DNA were added to 20 μL cell-free reactions and incubated at 29°C for 0, 30, 60 or 120 min and quickly submerged in liquid nitrogen to stop the reaction. Frozen samples were put on ice; and immediately, a volume of binding buffer from PCR clean-up kit (Promega, A9282) was added followed by 2 µL (300 ng) of the 500 bp linear DNA that served as an internal standard for the purification. The samples were then purified following standard supplier’s protocol and eluted with 30 µL of ultra-pure water. Next, 0.3 volumes of loading buffer were added to the purified samples and 10 µL were run on a 1% agarose gel electrophoresis containing 1X SYBR-Safe for DNA visualization. 1.5 kb and 500 bp DNA fragments were placed in two independent lines along with another line for 1 kb Ladder (NEB, N232). Once bands were clearly identifiable, the gel was photographed on a blue LED light transilluminator with a blue-light filter. The intensity of the 1.5 kb bands in each sample was integrated using ImageJ and normalized with the intensity of the 500 bp band of the same lane.

We first sought to implement a low-cost and simple protocol for cell-free gene expression. To do this, we combined the use of S12 crude extracts–a simple post lysate processing which does not require ultracentrifugation nor dialysis (Kim et al., 2008)—with a highly concentrated amino acid mixture (Caschera and Noireaux, 2015b) and a cost-effective energy source. This energy source is based on maltodextrin and polyphosphates, which do not require cold-chain transportation (Caschera and Noireaux, 2015a). We characterized our system by measuring the dynamics or endpoints of the pT7:sfGFP constitutive expression (Figure 1A). Initially, we prepared four different batches and tested optimum magnesium concentration in the reaction buffer for the cell-free expression of sfGFP. Optimal values ranged between 8.5 and 10 nM for all extracts (Supplementary Figure S2). With the goal of reducing the cost of lysate preparation, we compared maltodextrin and polyphosphates (HMP) to the conventional and more expensive 3-phosphoglyceric acid (3-PGA) energy source. In a side-by-side comparison with 3-PGA, maltodextrin produced a similar initial rate in sfGFP fluorescence (Supplementary Figure S3). Moreover, the endpoint measurements were significantly higher for the cost-effective maltodextrin-based energy source in each batch tested (Figure 1B). Next, we measured the dynamics of constitutive pT7:sfGFP (Figure 1A) expression in these extracts compared to two RNAP T7-based commercial kits. In comparison to these commercial cell-free systems, our in-house cell lysates generated higher endpoint fluorescent values, although variability was observed between different batches of cell-free extracts (Figure 1C).

A cost-breakdown analysis of lab-scale extract production of this optimized cell-free lysate system was performed, comparing reagent prices available to the collaborating institutions in Chile and the United Kingdom (Supplementary Tables S7–13). The cost per reaction (5 µL) in Chile was $0.069 USD for the maltodextrin-based preparation in comparison to $7.80 USD for the locally purchased commercial PURExpress, representing a reduction of two orders of magnitude. In comparison, the home-made preparations were about two times less expensive in the United Kingdom than in Chile (Supplementary Figure S4; Supplementary Table S7). Maltodextrin-based reactions were approximately 20% cheaper than the 3-PGA alternative.

To investigate whether RNA toehold sensors would be functional in the in-house prepared cell extracts, we used Zika virus (ZIKV) toehold sensors already shown to work well in PURExpress (Pardee et al., 2016). We selected ZIKV toehold sensors 8 and 27 and their respective triggers due to their high dynamic range and orthogonality (Pardee et al., 2016). These toehold sensors, controlling full-length LacZ expression, were incubated with the corresponding RNA trigger (400 nM) independently (Figure 2A). For each sensor, we chose the highest DNA concentration that ensures low-background in PURExpress and used this concentration for comparison with in-house cell-free reactions. Sensor 8 (at 0.8 nM plasmid DNA) behaved similarly in both reaction conditions, achieving a near-maximal response about 120 min after induction while maintaining a low signal in the absence of the trigger (Figure 2B). Sensor 27 (2 nM input DNA), also displayed comparable performance and sequence-specific activation in both systems used (Figures 2B,C). We also compared the performance of the full-length LacZ with LacZ-alpha reporters supplemented with the previously expressed LacZ-omega peptide in commercial and in-house cell-free extracts (Supplementary Figure S5). Full-length LacZ reporters exhibited higher ON/OFF endpoint absorbance values in both systems tested (Supplementary Figure S6, right). This can be explained by the slightly higher OFF state observed on both toehold sensors when using LacZ-alpha as a reporter (Supplementary Figure S6).

Next, we studied the effect of plasmid DNA input concentration on the leaky expression and saturation of sensing reactions. We tested three ZIKV toehold sensors controlling full-length LacZ expression (ZIKV Sensors 8, 27, and 32) (Pardee et al., 2016) in concentrations ranging from 0.5 to 10 nM. In all sensors, OFF state signal increased as a function of the input DNA concentration (Supplementary Figure S7). These results indicate that input DNA concentration can affect the dynamic range of RNA toehold sensors and that optimal concentrations may be different for each sensor.

To increase the sensitivity of CFTS in home-made cell-free preparations, we performed NASBA amplification of the target RNA before adding it to the reactions containing the sensors (Pardee et al., 2016). While unamplified RNA was detected at concentrations no lower than 3 nM, the NASBA amplification of target RNAs upstream in the workflow permitted the detection of RNA at concentrations as low as three fM (Figure 2D), representing a sensitivity increment of six orders of magnitude.

Deployment of RNA sensors in point-of-care settings is facilitated by the lyophilization of cell-free reactions, enabling room temperature transportation and use upon rehydration (Pardee et al., 2016). In order to test whether home-made CFTS can also be freeze-dried and stored at room-temperature, we lyophilized reactions supplemented with pT7:sfGFP plasmid. These reactions were sealed immediately after lyophilization and kept at room temperature for up to 90 days in a closed tupperware containing desiccant and, upon rehydration, compared to a fresh sample for reference. We observed more than 60% recovery of the endpoint sfGFP expression 1 week after lyophilization, which decreased to 17% after 90 days at room temperature (Supplementary Figure S8). The ZIKV Sensor 27 was also tested in home-made cell extracts after one and 7 days of lyophilization. Besides the evident decrease in dynamic range, especially after 7 days, these reactions retained the ability to detect its target trigger, while maintaining target specificity (Supplementary Figure S9). Taken together, these results indicate that the home-made cell-free system is compatible with lyophilization both for constitutive protein expression and for toehold RNA sensing reactions. The efficiency loss during storage at room temperature indicates that the preservation conditions should be addressed for further optimization and the use of cryoprotectants (Karig et al., 2017).

The use of linear DNA for CFTS offers several advantages compared to plasmid DNA that has to be generated by cloning and then amplified using bacterial cultures prior to use (Yang et al., 1980; Bassett and Rawson, 1983; Hoffmann et al., 2001; Michel-Reydellet et al., 2005; Seki et al., 2008; Shrestha et al., 2012; Sun et al., 2014; Marshall et al., 2017). Linear DNA can be produced by PCR amplification from a lacZ gene template, enabling the design of toehold structures as primer tails for rapid screening of CFTS libraries. The use of linear dsDNA in cell-free, however, is affected by nuclease-mediated DNA degradation in crude cell extracts. This effect is primarily due to the action of exonuclease V (Yang et al., 1980; Bassett and Rawson, 1983) (encoded in the RecBCD operon) (Dillingham and Kowalczykowski, 2008) and endonuclease I (encoded by endA), which are the dominant sources of endonuclease activity in E. coli (I. R. Lehman et al., 1962). Previous studies have shown an increase in the efficiency of cell-free protein synthesis from PCR products using several approaches, such as supplementing with exonuclease V inhibitors (Sitaraman et al., 2004; Sun et al., 2014), using modified nucleotides downstream the PCR reaction (Hoffmann et al., 2001), incorporating competitive DNA strands containing χ-sites (Marshall et al., 2017), adding dsDNA binding proteins (Zhu et al., 2020), depleting exonuclease V in the crude extracts (Seki et al., 2008), deleting RecBCD with the lambda phage red recombinase (Michel-Reydellet et al., 2005), and generating strains lacking endA (Michel-Reydellet et al., 2005; Hong et al., 2015).

To increase the stability of PCR-derived linear DNA, we explored a CRISPRi-based strategy (Larson et al., 2013) to control the genes encoding exonuclease V and endonuclease I in cells before harvesting. We designed sgRNAs targeting the 5’ ends of these genes and an IPTG-inducible dCas9 (Supplementary Figure S10A–C) and transformed E coli strain BL21 DE3 STAR (hereafter named CRISPRi+). As a control, an off-target sgRNA that does not have a known target in the E.coli genome (Nuñez et al., 2017) was transformed into E coli strain BL21 DE3 STAR and tested in parallel (hereafter named CRISPRi-). A growth comparison was performed between the CRISPRi+, CRISPRi- and the basal genotype strain BL21 DE3 STAR, finding a slightly lower growth rate for the CRISPRi+ (Supplementary Figure S10D).

This CRISPRi strategy is cost-effective as it does not require the supplementation with extra components, or in vitro modifications of the PCR product. To test this approach, our crude extracts of each genotype (BL21 DE3 STAR/CRISPRi+, BL21 DE3 STAR/CRISPRi- and BL21 DE3 STAR) were prepared and the stability of a 1.5 Kb linear DNA was quantified over a 2-h time course using agarose gel electrophoresis (Supplementary Figure S11A). The following exponential degradation model was fitted to the data: D N A ( t ) = D N A 0 ⋅ e − K d e g t where D N A 0 is the initial concentration of DNA, D N A ( t ) is the remaining concentration of DNA at a given time t , and K d e g the degradation rate of the DNA. Modelling was undertaken assuming the lower plateau equal to zero, and the ordinary least squares approach was used for parameter estimation. Model screening indicated no statistical evidence of the parameters D N A 0 being different across the data sets evaluated (F-test for extra sum of squares, p = 0.9285), finding the best fit value at D N A 0 = 0.9797 (Supplementary Figure S11B). Statistical analysis of the K d e g parameters showed significant differences between cell extract genotypes (F-test for extra sum of squares, p < 0.001). Degradation rate decreased significantly between the CRISPRi-optimized extracts ( K d e g = 0.008 / m i n ) to the two controls ( K d e g = 0.022 / m i n for the CRISPRi-negative control, and K d e g = 0.040 / m i n for the BL21-derived crude extract). Also, the CRISPRi optimized extracts significantly increased protein production capacity from PCR products, leading to a two-fold increase in the sfGFP endpoint signal (Supplementary Figure S12A).

Plasmid-derived endpoint expression was also measured in the three genotypes. No statistical differences were found between these values (Supplementary Figure S12B). The linear/plasmid ratio of end-point sfGFP fluorescence was also calculated for each batch, revealing statistical differences between CRISPRi+ and each of the other two genotypes (Supplementary Figure S12C). Taken together, these results indicate that CRISPRi + strain enhances stability of linear DNA, and increases expression yields of sfGFP from PCR-derived linear templates.

We observed a small increase in variability in the PCR-derived linear DNA expression of sfGFP with respect to the expression from plasmid DNA. This was observed across the three genotypes, with coefficients of variability of 0.89 and 1.29 for the expression of sfGFP in CRISPRi+ from plasmid and linear DNA, respectively (Supplementary Table S14).

We prepared CRISPRi-optimized extracts using the BL21-Gold-dLac strain and tested the RNA sensing capability of ZIKV toehold sensors expressed directly from PCR linear products. Using these CRISPRi extracts, both ZIKV sensors, 8 and 27, were able to detect RNA in a sequence-specific manner and behaved similarly to the plasmid derived sensors (Supplementary Figure S13). Subsequently, we used these CRISPRi-optimized crude extracts to prototype novel RNA sensors for Potato Virus Y (PVY), a virus affecting local agriculture in Chile. First, we selected a conserved sequence from a wide range of PVY strains (Supplementary Figure S14), which was subsequently generated as a synthetic fragment, transcribed in vitro and used for screening potential toehold sensors (Figure 3; Supplementary Table S5, 6).

The majority of published toehold sensors have been designed with NUPACK, a software tool for modeling the thermodynamics properties of DNA and RNA molecules (Green et al., 2014; Pardee et al., 2016; Ma et al., 2018). In this work, we have implemented an algorithm that leverages NUPACK and can be generally applied to the analysis and design of novel toehold sensors according to ideal designs (Supplementary Figure S1). Using NupackSensors (see Methods), we analyzed the consensus sequence identified previously and selected eight different toehold RNA sensors for experimental screening. Transcriptional units encoding for each PVY sensor were prepared by PCR amplification and incubated with synthetic RNA direct or reverse complementary (RC) to test their ability to detect RNA in a sequence-specific manner (Figure 3A; Supplementary Figure S15). A control without RNA was used as a baseline in the ON/OFF endpoint calculations. Among the eight sensors tested, two PVY sensors had ON/OFF endpoint measurements greater than two and background level lower than 1.2 (Figure 3B).

In order to validate the fast characterization of PVY toehold sensors using PCR-derived linear DNA, the best scored sensors (PVY Sensor one and PVY Sensor 7) were cloned in plasmids and compared side by side to the plasmid version of ZIKV Sensor 27 in a gradient of input DNA concentrations ranging from 1 to 4 nM (Supplementary Figure S16). Consistent with previous observations (Supplementary Figure S7), input DNA concentrations affect the performance of the toehold sensors. Some sensors (e.g. PVY Sensor 7) showed significant background activation (i.e., being active without a trigger) (Supplementary Figure S16). This background activation is proportional to input DNA concentration. The best performance of PVY Sensor seven was found at a lower concentration (1–2 nM) than for PVY Sensor 1, whose optimal concentration was between 2 and 4 nM (Supplementary Figure S16). Once a good working concentration was identified, PVY Sensor one and ZIKV Sensor 27 were incubated in home-made cell-free reactions (at 3.5 nM final concentration) and supplemented with ZIKV Trigger 27 or PVY RNA (at 480 nM final concentration). PVY Sensor one displayed sequence-specific activation comparable with ZIKV Sensor 27 (Figure 3C). These results showed that the fast-prototyping pipeline presented here, followed by an optimization of input DNA concentration, is a suitable strategy for identifying novel RNA toehold sensors of good performance.