The authors would like to thank Ekaterina V. Nikitina for kindly providing gDNA of EBV. Muhannad Ateiah, Maria Y. Berezovskaya, and Maria S. Rubel thank the Ministry of Education and Science of the Russian Federation (Grant No FSER-2022-0009) and the Priority 2030 program.

1. DNM design
<ol>
	<li>Select a unique region within the genome of interest. 
	NOTE: This work uses a region of the Epstein-Barr virus (EBV) genome in positions 13972-14154 (OR652423.1).</li>
	<li>Create a primer set for the amplification of the selected fragment, for example, via Primer3 tool embedded in Ugene26.</li>
	<li>Open the UNAFold web tool27 (see Table of Materials) and insert the selected region. Change&#160;the folding temperature to 55 &#176;C, and ionic conditions to 250 mM of monovalent ions, and 200 mM of Mg2+.
	<ol>
		<li>Open the resulting secondary structure of the ssDNA fragment and select a stable hairpin. Locate the DNA-nanomachines&#39; binding site in the&#160;unstructured regions or, alternatively, on the loops of the hairpin structures to achieve a stronger binding of the target.</li>
	</ol>
	</li>
	<li>If the targeted analyte site is folded in a stem-loop structure, place Arm 1 and 2 as follows: Ensure that Arm 2 binds one side of the stem, the loop, and 3-5 nt of the second stem side; Arm 1 binds a fragment of the second stem side.</li>
	<li>Open the DinaMelt tool28 (see Table of Materials) and analyze the sequences of the arms and their reverse-complement sequences. Use the DinaMelt tool to make sure that the Tm of Arms 2 and 3 is above 65 &#176;C: at least 10 &#176;C above the assay temperature (55 &#176;C).
	<ol>
		<li>Keep the Tm of Arm 1 at least 1-3 &#176;C above the reaction temperature (55&#160;&#176;C) if high recognition selectivity is&#160;to be achieved29.</li>
	</ol>
	</li>
	<li>Combine Arms 1 and 2 sequences with the DNAzyme core&#39;s halves and the F-sub binding fragments13.</li>
	<li>Analyze the secondary structure of the designed DNA strands using UNAFold27. 
	NOTE: 55 &#176;C (assay temperature), 200 mM Mg2+, 250 mM monovalent ions (HEPES, Na+, K+).
	<ol>
		<li>Use the design only if the folding &#916;G is lower than - 4 kcal/mol. Try to avoid long CG-rich sequences. If the secondary structure is too stable, introduce a mutation to the Arm to increase the folding &#916;G30. Alternatively, placing Arm 3 2-3 nt away from Arm 2 is another strategy to change the Arm 3&#160;sequence to avoid stable intermolecular structures.</li>
	</ol>
	</li>
	<li>Create a random sequence for the DNA tile fragment as long as Arm 3. Combine the Arm 3 sequence with the DNA tile sequence via (dT)4-6 or ethylene glycol (e.g., triethylene glycol (TEG) or hexaethylene glycol (HEG)). The DNM version presented in the experiment uses (dT)6.</li>
	<li>Link Arm 2 with the sequence complementary to the DNA tile fragment selected in step 1.8 via a linker.</li>
	<li>Analyze the secondary structure of the designed DNA strands using the UNAFold web app. Ensure that the folding energy of each DNA strand is above 4 kJ/mol at 55 &#176;C, and avoid long CG-enriched sequences. Preferably, change the DNA tile sequence.</li>
	<li>Draw the structure using any available vector graphics software. This article uses Biorender and Pixelmator Pro for visualization (see Table of Materials). Verify accuracy in 5&#39;-&#62;3&#39; directions for each strand. 
	NOTE: Obtain the sequences from a reliable commercial vendor.</li>
</ol>
2. Functional test of the DNM
<ol>
	<li>Preparation of buffer and reagents
	<ol>
		<li>Prepare the&#160;reaction buffer composed of 50 mM HEPES (pH 7.5-7.8), 50 mM NaCl, 150 mM KCl, and 200 mM MgCl2. Fill with the&#160;deionized water up to 50 mL.</li>
		<li>Prepare 10 &#181;M aliquots of Dzb-Tile and Tile-Arm3 oligonucleotides. Prepare 1 &#181;M solution of the Dza, a 100 &#181;M F-sub, and 1 nM, 10 nM, 100 nM analytes in RNase/free water or sterile deionized water. The details of the oligonucleotide sequences are provided in the Table of Materials.</li>
	</ol>
	</li>
	<li>DNM assembly
	<ol>
		<li>Thaw the oligonucleotide solutions completely before using. Gently mix by tapping (do not intensively vortex). Spin down (rapidly, for a few seconds) the solution using a microcentrifuge.</li>
		<li>Mix 1 &#181;M each of Dzb-Tile and Tile-Arm3 in 200 &#181;L of the reaction buffer in 0.5 mL microcentrifuge tubes.</li>
		<li>Mix the tube gently and spin down the solution.</li>
		<li>Wrap the lid of the closed tube with paraffin film. Alternatively, use screw cap tubes.</li>
		<li>Incubate the tube into a 500 mL beaker with boiling water for 2 min, then turn the heater off and let the temperature passively cool down overnight.</li>
		<li>Prepare the 12% native PAGE: Mix 1 mL of 10&#1093; TBE buffer, 3 mL of 40% AA:BA, deionized water up to 10 mL, 50 &#181;L of APS, and 5 &#181;L of TEMED (see Table of Materials). Move the mixture to the gel cassette and let it polymerize.</li>
		<li>Mix 1 &#181;L of each sample, namely, the assembled DNM, Dzb-Tile, and Tile-arm3, with 1 &#181;L of 4x loading dye and load them into the gel.</li>
		<li>Put the cassette into the chamber, fill it with 1x TBE buffer, and let the gel run for 90 min at 80 V.</li>
		<li>Dye the gel with Ethidium bromide and visualize it using a gel-documenting system (see Table of Materials).</li>
	</ol>
	</li>
	<li>LOD assay
	<ol>
		<li>Prepare 160 &#181;L of 200 nM F-sub in the reaction buffer. This is done to assess the basic background of the substrate stability.</li>
		<li>Prepare 7 aliquots of 160 &#181;L of preassembled DNM, F-sub, and Dza at concentrations of 20 nM of DNM and Dza and 200 nM of F-sub in the reaction buffer. Out of the seven tubes, keep tube #1 as the blank background to assess the spontaneous assembly of the DNAzyme core.</li>
		<li>Add the analyte into tubes #2-7 at the final concentrations of 1 pM, 10 pM, 100 pM, 200 pM, 500 pM and 1000 pM.</li>
		<li>Gently mix, spin down the tubes, and classify&#160;the solutions into three 50 &#181;L portions into a&#160;black 96-well plate. Seal the plate with an optically transparent film.</li>
		<li>Incubate the plate in a water bath at 55 &#176;C for 1 h. Spin down the plate.</li>
		<li>Measure fluorescence at 525 nm (&#955;ex = 495 nm). Calculate the mean and the standard deviation for each point.</li>
		<li>Calculate the blank-to-basic ratio by dividing the signal of the tube that contains F-sub and DNM by the signal of the tube that contains F-sub only. Ensure the ratio is within the 1.1-1.5 range.</li>
		<li>Calculate the signal-to-blank ratio by dividing the signal of the tube that contains F-sub, DNM, and the analyte to the signal of the tube that contains F-sub and DNM only. Consider the signal as true positive if it is higher than the background average plus three standard deviations.</li>
		<li>Repeat the experiment twice and ensure the standard deviation between the analytical repeats is less than 0.5.</li>
	</ol>
	</li>
</ol>

Precision DNAzyme Nanomachines for Discriminative RNA and DNA Analysis

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The authors declare no conflict of interest.

The design of DNA machines is straightforward but requires some experience in designing&#160;hybridization probes or functional DNA nanostructures. It is appropriate to keep the analyte fragment as short as possible to diminish the number of possible secondary structures and simplify DNM invasion to the secondary structure. The CG content should preferably be below 60% to avoid stable intramolecular structures. Successful assembly of the DNM is achieved at slow cooling rates. In some cases, DNMs can be spontaneously asse...

One of the earliest methods for&#160;nucleic acid detection is&#160;complementary binding of selective oligonucleotides to the analyzed RNA or DNA sequences. This method employs nucleic acid fragments (probes) that can form Watson-Crick base pairs with a targeted DNA or RNA analyte1. The complex is then differentiated from the analyte and the unbound probe by a variety of techniques. Certain methods, such as Northern blotting, in situ hybridization, or qPCR, are based on the&#160;phenomenon&#160;of complementary binding2. The most common hybridization probes have two significant drawbacks: low sensitivity (they can reach micromolar to nanomolar levels) as well as low selectivity to single nucleotide variations (SNV), including point mutations. The issue requires a sophisticated approach since the solutions to these drawbacks conflict with each other3. To provide the best selectivity, the detecting oligonucleotide should be kept short enough to form unstable hybrids with mismatched analytes. Such short oligonucleotides are not able to bind targeted nucleic acids tightly and unwind their secondary structures, thus often failing to provide a detectable signal. It is especially challenging to detect CG-rich fragments in biological RNA, or double-stranded DNA (dsDNA). On the other hand, long probes are insensitive to SNV3. To break the deadlock, the concept of a binary probe has been&#160;developed4.
Binary sensors split a single detection probe into two pieces and specialize its fragments, keeping one of them long to unwind the hairpins or invade the dsDNA. The second binary probe fragment remains short to be sensitive to a mismatched base, thus providing a means for detecting SNV. The signal will be produced if the two binary sensor parts are joined together4. The full complex can be visualized via FRET5, molecular beacon probe6,7, or G-quadruplexes with peroxidase-like activity8,9,10, or else RNA-cleaving11,12,13 DNAzyme. Binary sensors with a 10-23 DNAzyme core have been amply described. They have been adapted to detect single-stranded nucleic acid fragments&#160;created synthetically11, or single-stranded amplification products14,15. Detection without amplification is also possible, for example, in the case of 16S rRNA extracted from a cell culture, since this molecule is abundant in cells12,16. Binary sensors with a 10-23 DNAzyme core can also be adapted for non-nucleic acid detection, such as for lead ions17. Nevertheless, low sensitivity is still considered to be one of the major drawbacks of binary 10-23 DNAzyme sensors, and&#160;various approaches, including cascades18 or alternative signal-enhancing methods19, have been developed to address this issue. Unfortunately, the above techniques drastically increase the cost and instability of the sensor components, and so they have not come into practice.
The experiment described in this work uses 10-23 DNAzyme-based DNA-nanosensors referred to as DNA-nanomachines (DNM)20,21. These structures include binary sensors and also&#160;(1) DNA facilitators flanking the binary probe,&#160;unwinding the structured regions and&#160;invading into double-stranded DNAs, and (2) a DNA tile that holds all the DNM parts together in close proximity and increases the chances of signal formation (Figure 1). Altogether, the 10-23 DNAzyme-based DNMs decrease the limit of detection (LOD) down to the picomolar range21; they can be used to detect 16rRNA in cell lysates22 or report the presence of viral RNA without amplification23,24. At the same time, the DNMs remain sensitive to the SNV and can even be used to genotype alleles in heterozygous organisms25. The DNM method can be used as a complementary technique to any amplification type for product visualization or identification of the product in a complex mixture with high selectivity. The DNMs, unlike conventional TaqMan and beacon probes, do not require heating of the sample and so can be used in end-point detection protocols, making the overall detection cost-effective.
This article describes the in silico development of a DNM and demonstrates procedures for assembly and functional characterization of DNM. The work was performed using a synthetic fragment of Epstein-Barr virus (EBV) corresponding to the positions 13972-14154 of the viral DNA (OR652423.1) (see Table of materials).

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1.5 mL tube</td>
			<td>Biofil</td>
			<td>CFT011015</td>
			<td></td>
		</tr>
		<tr>
			<td>100 bp+ DNA Ladder</td>
			<td>Evrogen</td>
			<td>NL002</td>
			<td></td>
		</tr>
		<tr>
			<td>100-1000 &#181;L pipette</td>
			<td>Kirgen</td>
			<td>KG-Pro1000</td>
			<td></td>
		</tr>
		<tr>
			<td>10-100 &#181;L pipette</td>
			<td>Kirgen</td>
			<td>KG-Pro100</td>
			<td></td>
		</tr>
		<tr>
			<td>1-10 &#181;L pipette</td>
			<td>Kirgen</td>
			<td>KG-Pro10</td>
			<td></td>
		</tr>
		<tr>
			<td>20-200 &#181;L pipette</td>
			<td>Kirgen</td>
			<td>KG-Pro200</td>
			<td></td>
		</tr>
		<tr>
			<td>2-20 &#181;L pipette</td>
			<td>Kirgen</td>
			<td>KG-Pro20</td>
			<td></td>
		</tr>
		<tr>
			<td>4x Gel Loading Dye</td>
			<td>Evrogen</td>
			<td>PB020</td>
			<td></td>
		</tr>
		<tr>
			<td>Acrylamide 4K</td>
			<td>AppliChem</td>
			<td>A1090,0500</td>
			<td></td>
		</tr>
		<tr>
			<td>Ammonium persulfate</td>
			<td>Carl Roth</td>
			<td>2809447</td>
			<td></td>
		</tr>
		<tr>
			<td>Biorender</td>
			<td>Biorender</td>
			<td></td>
			<td>https://www.biorender.com</td>
		</tr>
		<tr>
			<td>Bisacrylamide</td>
			<td>Molekula</td>
			<td>22797959</td>
			<td></td>
		</tr>
		<tr>
			<td>Boric Acid</td>
			<td>TechSnab</td>
			<td>H-0202</td>
			<td></td>
		</tr>
		<tr>
			<td>ChemiDoc imaging system</td>
			<td>BioRad</td>
			<td>12003153</td>
			<td></td>
		</tr>
		<tr>
			<td>Costar 96-Well Black Polystyrene Plate</td>
			<td>Corning</td>
			<td>COS3915</td>
			<td></td>
		</tr>
		<tr>
			<td>DinaMelt</td>
			<td>RNA Institute</td>
			<td></td>
			<td>http://www.unafold.org/Dinamelt/applications/two-state-melting-hybridization.php</td>
		</tr>
		<tr>
			<td>EDTA</td>
			<td>Amresco</td>
			<td>Am-O105</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethidium bromide</td>
			<td>BioLabMix</td>
			<td>EtBr-10</td>
			<td></td>
		</tr>
		<tr>
			<td>HEPES</td>
			<td>Amresco</td>
			<td>Am-O485</td>
			<td></td>
		</tr>
		<tr>
			<td>Magnesium chloride</td>
			<td>AppliChem</td>
			<td>131396</td>
			<td></td>
		</tr>
		<tr>
			<td>Mini Protean Tetra Cell</td>
			<td>BioRad</td>
			<td>1658001EDU</td>
			<td></td>
		</tr>
		<tr>
			<td>pipette 10 &#181;L tips</td>
			<td>Kirgen</td>
			<td>KG1111-L</td>
			<td></td>
		</tr>
		<tr>
			<td>pipette 1000 &#181;L tips</td>
			<td>Kirgen</td>
			<td>KG1636</td>
			<td></td>
		</tr>
		<tr>
			<td>pipette 200 &#181;L tips</td>
			<td>Kirgen</td>
			<td>KG1212-L</td>
			<td></td>
		</tr>
		<tr>
			<td>Pixelmator Pro</td>
			<td>Pixelmator Team</td>
			<td></td>
			<td>https://www.pixelmator.com/pro/</td>
		</tr>
		<tr>
			<td>Potassium chloride</td>
			<td>Carl Roth</td>
			<td>1782751</td>
			<td></td>
		</tr>
		<tr>
			<td>PowerPac Basic Power Supply</td>
			<td>BioRad</td>
			<td>1645050</td>
			<td></td>
		</tr>
		<tr>
			<td>RNAse/DNAse free water</td>
			<td>Invitrogen</td>
			<td>10977049</td>
			<td></td>
		</tr>
		<tr>
			<td>Sealing film for PCR plates</td>
			<td>Sovtech</td>
			<td>P-502</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium chloride</td>
			<td>Vekton</td>
			<td>HCh (0,1)</td>
			<td></td>
		</tr>
		<tr>
			<td>Spark multimode microplate reader</td>
			<td>Tecan</td>
			<td>Spark- 10M</td>
			<td></td>
		</tr>
		<tr>
			<td>T100 amplificator</td>
			<td>BioRad</td>
			<td>10014822</td>
			<td></td>
		</tr>
		<tr>
			<td>TEMED</td>
			<td>Molekula</td>
			<td>68604730</td>
			<td></td>
		</tr>
		<tr>
			<td>Tris(hydroxymethyl)aminomethane</td>
			<td>Amresco</td>
			<td>Am-O497</td>
			<td></td>
		</tr>
		<tr>
			<td>UNAFold</td>
			<td>RNA Institute</td>
			<td></td>
			<td>http://www.unafold.org/mfold/applications/dna-folding-form.php</td>
		</tr>
		<tr>
			<td>Water bath</td>
			<td>LOIP</td>
			<td>LB-140</td>
			<td></td>
		</tr>
		<tr>
			<td>Oligos used</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Analyte:</td>
			<td rowspan="2">Evrogen</td>
			<td rowspan="2"></td>
			<td rowspan="2">direct order, standard desalting purification</td>
		</tr>
		<tr>
			<td>GAGCACTTGGTCAGGCACACGG 
			ACAGGGTCAGCGGAGGACGCG 
			TGGCACAGCAGCCCGGGGTAG 
			GTCCCCTGGACCTGCCGCTGG 
			CGGACTACGCCTTCGTTGC</td>
		</tr>
		<tr>
			<td>Tile-Arm3:</td>
			<td rowspan="2">Evrogen</td>
			<td rowspan="2"></td>
			<td rowspan="2">direct order, standard desalting purification</td>
		</tr>
		<tr>
			<td>CCG GGCTGCTGTGCCATTTT 
			TTGCTGACTACTGTCACCTCT 
			CTGCTAGTCT</td>
		</tr>
		<tr>
			<td>Dzb-Tile: AGACTAGCAGAGAGGTGACAG 
			TAGTCAGCTTTTTTCGCGTCCTC 
			CGCTGACCACAACGAGAGGAA 
			ACCTT</td>
			<td>Evrogen</td>
			<td></td>
			<td>direct order, standard desalting purification</td>
		</tr>
		<tr>
			<td>Dza: TGCCCAGGGAGGCTAGCTCT 
			GTCCGTGTGCCTGACCA</td>
			<td>Evrogen</td>
			<td></td>
			<td>direct order, standard desalting purification</td>
		</tr>
		<tr>
			<td>F-sub oligonucleotide: AAGGTT(FAM)TCCTCrGrU 
			CCCTGGGCA-BHQ1</td>
			<td>DNA-Syntez</td>
			<td></td>
			<td>direct order, HPLC purification</td>
		</tr>
	</tbody>
</table>

dnazyme 10-23 - based nanomachines for nucleic acid recognition

DNAzyme-based nanomachines (DNM) for the detection of DNA and RNA sequences (analytes) are multifunctional structures made of oligonucleotides. Their functions include tight analyte binding, highly selective analyte recognition, fluorescent signal amplification by multiple catalytic cleavages of a fluorogenic reporter substrate, and fluorogenic substrate attraction for an increase in sensor response. Functional units are attached to a common DNA scaffold for their cooperative action. The RNA-cleaving 10-23 DNMs feature&#160;improved sensitivity in comparison with non-catalytic hybridization probes. The stability of the DNM and the increased chances of substrate recognition are provided&#160;by a double-stranded DNA fragment,&#160;a tile. DNM can differentiate two analytes with a single nucleotide difference in a folded RNA and a double-stranded DNA and detect analytes at concentrations ~1000 times lower than other protein-free hybridization probes. This article presents the concept behind the diagnostic potential of DNA-nanomachine activity and overviews DNM design, assembly, and application&#160;in nucleic acid detection assays.

Author Spotlight: Advancements in DNA Nanosensors &amp;#8211; Addressing Sensitivity and Selectivity Challenges in Molecular Detection

DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition

The biggest breakthrough our lab made in the field of hybridization probe was made in 2007 by Dmitry Kolpashchikov, who suggested an ADL splitting hybridization probes in halves assessing each of the half its own function, for example, increasing selectivity to mismatches and single nucleotide variations along to unwinding complex probes. The second breakthrough was made a decade later when it was suggested to add additional multi component binding arms. Along with the Unitan platform.Such designs were able to work even with complex targets, for example, double stranded nucleic acids, and highly structured nucleic acids. The biggest challenges our lab faces right now are coming from the problem of low sensitivity of DNA nano sensors in comparison to conventional amplification techniques. By now, the DNA nano sensors in amplification free assay presents low selectivity, and we are trying to overcome this problem with new molecular designs and new ways of DNA nano sensor detection.The main advantages of our DNA sensors are their sensitivity in terms of low detected concentration of the analyte and selectivity. For example, their ability to detect single nucleotide polymorphism Also as an advantage compared to other diagnostics techniques. Our DNA sensors are able to unwind and detect complex RNA structures and double stranded DNA.The new scientific question, our results have paved the way for is, is it possible to find double stranded DNA using protein free hybridization props? The protein independent prop could be easily accessible by automated DNA synthesis, easier to be delivered in cells and be compatible with chemical modification and complex nano structures developed by DNA nanotechnology combined with DNA enzymes such as Dnase lipids and DNA enzymes. Such a prop could become a basis for protein free nucleases a useful tool for gene editing and therapy.

The aim of the first experiment was to show the assembly of the DNM before&#160;the synthetic fragment of the analyte. All the constituent DNM strands were added to the reaction buffer and assembled in the beaker. The assembled DNM complex was assessed for its correct size and homogeneity by native PAGE. Native PAGE shows the assembled DNM with the analyte in lane 1 and two DNM strands in lanes 2 and 4. If the DNA nanomachine were&#160;not assembled, 2 or 3 separate bands would be visible instead of a single low-mobility...

Read this Scientific Article Protocol about DNAzyme 10-23 - Based Nanomachines for Nucleic Acid Recognition at JoVE.com

The DNAzyme-based nanomachines can be used for highly selective and sensitive detection of nucleic acids. This article describes a detailed protocol for the design of DNAzyme-based nanomachines with a 10-23 core using free software and their application in the detection of an Epstein-Barr virus fragment as an example.

DNAzyme-based nanomachines (DNM) for the detection of DNA and RNA sequences (analytes) are multifunctional structures made of oligonucleotides. Their ...

dnazyme-10-23-based-nanomachines-for-nucleic-acid-recognition

Research

JoVE Journal

Biochemistry

Designing DNAzyme-Based Nanomachines with a 10-23 Core for Detection of an Epstein-Barr Virus Fragment

To begin, open the UNA fold web tool and insert the selected genomic region of interest. Modify the folding temperature to 55 degrees Celsius. The concentration of monovalent ions to 250 millimolars and the magnesium ion concentration to 200 millimolars.Next, open the resulting secondary structure of the single stranded DNA fragment and select a stable hairpin structure. Locate the DNA nano machines binding site either in unstructured regions or on the loops of the hairpin structures for enhanced binding efficiency. If the target analyte site exhibits a stem loop structure, place arm two on one side of the stem covering the loop and three to five nucleotides on the second stem side.Position arm one on a fragment of the second stem side. Now open the DINAMelt tool and examine the sequences of both the arms and their reverse complement sequences. Combine arms one and two sequences with the DNAzyme cores halves, and the F-sub binding fragments.Next, construct a random sequence for the DNA tile fragment, ensuring it is not shorter than the length of arm three. Combine this sequence with the arm three sequence using a linker. Connect arm two to a sequence that is complimentary to the DNA tile fragment via a suitable linker.At last, using the UNA fold web app, analyze the secondary structure of the newly designed DNA strands.

Assembly of DNAzyme-Based Nanomachines for its Functional Characterization

To begin, design DNAzyme-based nanomachines, or DNM, with a 10 to 23 core, using free software. Obtain the designed sequences from commercial sources. Then, take 0.5 milliliter microcentrifuge tubes with 200 microliters of the reaction buffer.Add DZB-Tile and Tile-arm3 oligonucleotides to the tubes. Gently mix them and spin down the solution. Wrap the lid of the closed tube with paraffin film or use screw cap tubes.Incubate the tube in a 500 milliliter beaker with boiling water for two minutes. Then, turn the heater off and allow the temperature to passively cool down overnight. Now, prepare the 12%native page using the given reagents.Transfer the mixture to the gel cassette and allow it to polymerize. Mix one microliter of each sample with one microliter of four times loading dye and load them into the gel. Place the cassette into the chamber.Fill it with TBE buffer and run the gel for 90 minutes at 82 to 100 volts. Dye the gel with ethidium bromide and visualize it using a gel documenting system.

Limit of Detection (LOD) Assay to Check the Sensitivity of DNAzyme-Based Nanomachines (DNM)

To begin, design DNAzyme-based nano machines, or DNM, with a 10 to 23 core, using free software. Assemble the DNM and check its size and homogeneity by native page. Then prepare 160 microliters of F-sub in the reaction buffer.Prepare seven aliquots of 160 microliters of preassembled DNM, F-sub, and DZA in the reaction buffer. Add the analyte to tubes two to seven, and gently mix the components. Then spin down the tubes and divide the solutions into three 50-microliter portions in a black 96-well plate.Seal the plate with an optically-transparent film. Incubate the plate in a water bath at 55 degrees Celsius for one hour. Then spin down the plate.Afterward, measure fluorescence at 480 nanometers excitation wavelength, and 525 nanometers emission wavelength.

629 Views.  ITMO University.  The DNAzyme-based nanomachines can be used for highly selective and sensitive detection of nucleic acids. This article describes a detailed protocol for the design of DNAzyme-based nanomachines with a 10-23 core using free software and their application in the detection of an Epstein-Barr virus fragment as an example.

Precision DNAzyme Nanomachines for Discriminative RNA and DNA Analysis

Summary