This work was supported by the Research Corporation for Scientific Advancement (Cottrell College Scholar Award #22548) and by TriLink Biotechnologies (ResearchReward Grant #G139).&#160;

1. Activity Assay
NOTE: There are two typical types of assays that are often run to characterize DNA polymerases using the methods described here. They differ in whether they qualitatively characterize overall synthesis (encompassing many steps of DNA synthesis) or whether they quantitatively focus on individual steps. We describe the necessary steps for each of these below. 
NOTE: Because the assembly of materials are relatively complex, for time sensitive experiments, we recommend that al...

<ol>
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M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Directed+evolution+of+DNA+polymerases+for+next-generation+sequencing.">Directed evolution of DNA polymerases for next-generation sequencing.</a> Angew Chem Int Ed Engl. 49 (34), 5921-5924 (2010).</li><li>Xia, G., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Directed+evolution+of+novel+polymerase+activities:+mutation+of+a+DNA+polymerase+into+an+efficient+RNA+polymerase.">Directed evolution of novel polymerase activities: mutation of a DNA polymerase into an efficient RNA polymerase.</a> Proc Natl Acad Sci U S A. 99 (10), 6597-6602 (2002).</li><li>Chen, T., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Evolution+of+thermophilic+DNA+polymerases+for+the+recognition+and+amplification+of+C2'-modified+DNA.">Evolution of thermophilic DNA polymerases for the recognition and amplification of C2'-modified DNA.</a> Nat Chem. 8 (6), 556-562 (2016).</li><li>Thirunavukarasu, D., Chen, T., Liu, Z., Hongdilokkul, N., Romesberg, F. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Selection+of+2'-Fluoro-Modified+Aptamers+with+Optimized+Properties.">Selection of 2'-Fluoro-Modified Aptamers with Optimized Properties.</a> J Am Chem Soc. 139 (8), 2892-2895 (2017).</li><li>Taylor, A. I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Catalysts+from+synthetic+genetic+polymers.">Catalysts from synthetic genetic polymers.</a> Nature. 518 (7539), 427-430 (2015).</li><li>Alves Ferreira-Bravo, I., Cozens, C., Holliger, P., DeStefano, J. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Selection+of+2'-deoxy-2'-fluoroarabinonucleotide+(FANA)+aptamers+that+bind+HIV-1+reverse+transcriptase+with+picomolar+affinity.">Selection of 2'-deoxy-2'-fluoroarabinonucleotide (FANA) aptamers that bind HIV-1 reverse transcriptase with picomolar affinity.</a> Nucleic Acids Res. 43 (20), 9587-9599 (2015).</li><li>Schultz, H. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Taq+DNA+Polymerase+Mutants+and+2'-Modified+Sugar+Recognition.">Taq DNA Polymerase Mutants and 2'-Modified Sugar Recognition.</a> Biochemistry. 54 (38), 5999-6008 (2015).</li><li>Rosenblum, S. L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Design+and+discovery+of+new+combinations+of+mutant+DNA+polymerases+and+modified+DNA+substrates.">Design and discovery of new combinations of mutant DNA polymerases and modified DNA substrates.</a> Chembiochem. 18 (8), 816-823 (2017).</li><li>Creighton, S., Goodman, M. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gel+kinetic+analysis+of+DNA+polymerase+fidelity+in+the+presence+of+proofreading+using+bacteriophage+T4+DNA+polymerase.">Gel kinetic analysis of DNA polymerase fidelity in the presence of proofreading using bacteriophage T4 DNA polymerase.</a> J Biol Chem. 270 (9), 4759-4774 (1995).</li><li>Joyce, C. M., Benkovic, S. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=DNA+polymerase+fidelity:+kinetics,+structure,+and+checkpoints.">DNA polymerase fidelity: kinetics, structure, and checkpoints.</a> Biochemistry. 43 (45), 14317-14324 (2004).</li><li>Leconte, A. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Discovery,+characterization,+and+optimization+of+an+unnatural+base+pair+for+expansion+of+the+genetic+alphabet.">Discovery, characterization, and optimization of an unnatural base pair for expansion of the genetic alphabet.</a> J Am Chem Soc. 130 (7), 2336-2343 (2008).</li><li>Sanger, F., Nicklen, S., Coulson, A. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=DNA+sequencing+with+chain-terminating+inhibitors.">DNA sequencing with chain-terminating inhibitors.</a> Proc Natl Acad Sci U S A. 74 (12), 5463-5467 (1977).</li><li>Karger, B. L., Guttman, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=DNA+Sequencing+by+Capillary+Electrophoresis.">DNA Sequencing by Capillary Electrophoresis.</a> Electrophoresis. 30 (Suppl 1), S196-S202 (2009).</li><li>Lawyer, F. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=High-level+expression,+purification,+and+enzymatic+characterization+of+full-length+Thermus+aquaticus+DNA+polymerase+and+a+truncated+form+deficient+in+5'+to+3'+exonuclease+activity.">High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5' to 3' exonuclease activity.</a> PCR Methods Appl. 2 (4), 275-287 (1993).</li><li>Lawyer, F. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Isolation,+characterization,+and+expression+in+Escherichia+coli+of+the+DNA+polymerase+gene+from+Thermus+aquaticus.">Isolation, characterization, and expression in Escherichia coli of the DNA polymerase gene from Thermus aquaticus.</a> J Biol Chem. 264 (11), 6427-6437 (1989).</li><li>Carroll, S. S., Cowart, M., Benkovic, S. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+mutant+of+DNA+polymerase+I+(Klenow+fragment)+with+reduced+fidelity.">A mutant of DNA polymerase I (Klenow fragment) with reduced fidelity.</a> Biochemistry. 30 (3), 804-813 (1991).</li><li>Shendure, J., Ji, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Next-generation+DNA+sequencing.">Next-generation DNA sequencing.</a> Nat Biotechnol. 26 (10), 1135-1145 (2008).</li><li>Larsen, A. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+general+strategy+for+expanding+polymerase+function+by+droplet+microfluidics.">A general strategy for expanding polymerase function by droplet microfluidics.</a> Nat Commun. 7, 11235 (2016).</li><li>Cozens, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enzymatic+Synthesis+of+Nucleic+Acids+with+Defined+Regioisomeric+2'-5'+Linkages.">Enzymatic Synthesis of Nucleic Acids with Defined Regioisomeric 2'-5' Linkages.</a> Angew Chem Int Ed Engl. 54 (51), 15570-15573 (2015).</li></ol>

The authors have nothing to disclose.

Here, we have described an assay to characterize the DNA polymerase-mediated synthesis of M-DNA. By using near-infrared labeled DNA primers, and using denaturing polyacrylamide gel electrophoresis to resolve differently sized oligonucleotides, we can obtain single nucleotide resolution on oligonucleotides, enabling precise measurement of synthesis. These approaches can be used to either measure the overall activity of the enzyme (section 2.1) or to measure the Michaelis-Menten parameters of individual steps (note followi...

DNA polymerases perform accurate and efficient DNA synthesis and are essential to maintaining genome integrity. The ability to synthesize hundreds of nucleotides per second without making errors also makes DNA polymerases essential tools in molecular biology and biotechnology. However, these properties also limit the applications for M-DNA substrates; generally speaking, natural DNA polymerases cannot synthesize many potentially valuable M-DNA substrates, likely due to the high selective pressure against using non-standard substrates in vivo. Many groups have developed directed evolution approaches to generate mutant DNA polymerases capable of M-DNA synthesis1a,2,3,4,5; these efforts have expanded the biotechnological utility of DNA6,7,8.
To evaluate the ability of mutant DNA polymerases to synthesize M-DNA, we9,10, and others11,12,13 typically use in vitro measurements of DNA polymerase activity, which are described in this manuscript. In these experiments, DNA polymerases are co-incubated with a labeled primer/template duplex and nucleoside triphosphate substrates; the products are evaluated by gel electrophoresis. Depending on the specific experimental question, mutant DNA polymerases, modified primers, modified templates, or modified nucleoside triphosphates can be used, enabling the systematic biochemical evaluation of the mutant enzyme activity.
Historically, these assays have relied on a 5&#39; radioactive label to track DNA synthesis; most commonly, 32P and 33P have been used; typically, labeling is achieved using T4 polynucleotide kinase11. However, due to the finite lifetime and relatively high cost of radioactive labels and their safe disposal, our group instead uses a synthetic 5&#39; near-infrared fluorophore labeled DNA. Using a relatively low cost near-infrared gel imager, we have observed similar detection limits to prior studies using radioactive labels (unpublished results). We have successfully reproduced past observations9, and we have not observed any large quantitative difference with previously measured rate constants (unpublished results).
To analyze the size of DNA, and thus, the extent of DNA synthesis, we rely on polyacrylamide gel electrophoresis methods developed originally for Sanger sequencing14 before the advent of capillary electrophoresis15. The distance of separation or mobility can be used as a measurement of molecular weight; large format, vertical polyacrylamide gels can achieve single nucleotide resolution, enabling quantitative observation of DNA oligonucleotides of varying lengths.
Collectively, these experiments are a robust method for polymerase characterization. Due to the time sensitive nature of the reactions, preparation and care is necessary to achieve reproducible results. Further, while the acrylamide gel is a highly effective way to measure DNA synthesis, as well as numerous other DNA modifying reactions, with single nucleotide resolution, it can be technically challenging. The protocol here will hopefully enable users to perform these experiments while avoiding the most common mistakes.

<table>
	<tbody>
		<tr>
			<td>Tris HCl</td>
			<td>Promega</td>
			<td>H5123</td>
			<td></td>
		</tr>
		<tr>
			<td>Tris Base</td>
			<td>Promega</td>
			<td>H5131</td>
			<td></td>
		</tr>
		<tr>
			<td>MgCl2</td>
			<td>Fisher Scientific</td>
			<td>BP214-500</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetylated BSA</td>
			<td>Promega</td>
			<td>PR-R3961</td>
			<td></td>
		</tr>
		<tr>
			<td>KCl</td>
			<td>Sigma</td>
			<td>P4504</td>
			<td></td>
		</tr>
		<tr>
			<td>Dithiothreitol (i.e. DTT)</td>
			<td>Research Products International</td>
			<td>D11000</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethylenediaminetetraacetic acid (i.e. EDTA) (0.5M solution)</td>
			<td>Sigma</td>
			<td>03690-100mL</td>
			<td></td>
		</tr>
		<tr>
			<td>Glycerol</td>
			<td>Sigma</td>
			<td>G5516</td>
			<td></td>
		</tr>
		<tr>
			<td>Formamide</td>
			<td>Acros</td>
			<td>AC42374-5000</td>
			<td></td>
		</tr>
		<tr>
			<td>Orange G</td>
			<td>Sigma Aldrich</td>
			<td>O3756</td>
			<td></td>
		</tr>
		<tr>
			<td>Bromophenol blue</td>
			<td>Fisher Scientific</td>
			<td>50-701-6973</td>
			<td></td>
		</tr>
		<tr>
			<td>dNTPs</td>
			<td>Fisher Scientific</td>
			<td>FERR0191</td>
			<td></td>
		</tr>
		<tr>
			<td>M-dNTPs (riboNTPs)</td>
			<td>Fisher Scientific</td>
			<td>45-001-341 (343, 345, 347)</td>
			<td></td>
		</tr>
		<tr>
			<td>M-dNTPs (all other modified NTPs)</td>
			<td>TriLink Biotechnologies</td>
			<td>assorted</td>
			<td></td>
		</tr>
		<tr>
			<td>primer 1</td>
			<td>IDT DNA / TriLink Biotechnologies</td>
			<td>Custom Syntheses</td>
			<td>We use the IR700 dye which can be purchased as a custom synthesis. We typically purchase the oligonucleotides HPLC purified. Sequence is 5&#8217;-dTAATACGACTCACTATAGGGAGA</td>
		</tr>
		<tr>
			<td>template 1</td>
			<td>IDT DNA / TriLink Biotechnologies</td>
			<td>Custom Syntheses</td>
			<td>We typically purchase the oligonucleotides HPLC purified. Sequence is 5&#8217;-dCGCTAGGACGGCATTGGATCAGTCTCCCTATAGTGAGTCGTATTA</td>
		</tr>
		<tr>
			<td>Acrylamide</td>
			<td>Research Products International</td>
			<td>A11405</td>
			<td>38.67% acrylamide and 1.33% bis-acrylamide</td>
		</tr>
		<tr>
			<td>Tris/Borate/EDTA (TBE) solid</td>
			<td>Research Products International</td>
			<td>T22020</td>
			<td></td>
		</tr>
		<tr>
			<td>Urea ultrapure</td>
			<td>Research Products International</td>
			<td>U20200</td>
			<td></td>
		</tr>
		<tr>
			<td>Gel tape</td>
			<td>CBS Scientific</td>
			<td>GT-72-10</td>
			<td></td>
		</tr>
		<tr>
			<td>Large white spring clamp polypropylene</td>
			<td>CBS Scientific</td>
			<td>GPC-0001</td>
			<td></td>
		</tr>
		<tr>
			<td>Ammonium persulfate (APS)</td>
			<td>Fisher Scientific</td>
			<td>BP179</td>
			<td></td>
		</tr>
		<tr>
			<td>Tetramethylethylenediamine (TEMED)</td>
			<td>Fisher Scientific</td>
			<td>BP15020</td>
			<td></td>
		</tr>
		<tr>
			<td>0.75 mm spacers</td>
			<td>CBS Scientific</td>
			<td>SGS-20-0740A</td>
			<td></td>
		</tr>
		<tr>
			<td>33x42 Notched Glass Plate Set</td>
			<td>CBS Scientific</td>
			<td>SGP33-040A</td>
			<td></td>
		</tr>
		<tr>
			<td>Wedge plate separator</td>
			<td>CBS Scientific</td>
			<td>WPS-100</td>
			<td></td>
		</tr>
		<tr>
			<td>Comb for gel electrophoresis</td>
			<td>CBS Scientific</td>
			<td>SG33-0734</td>
			<td></td>
		</tr>
		<tr>
			<td>Gel electrophoresis rig</td>
			<td>CBS Scientific</td>
			<td>SG-400-33</td>
			<td></td>
		</tr>
		<tr>
			<td>ultrapure water</td>
			<td></td>
			<td></td>
			<td>we use a Milli-Q system from Millipore</td>
		</tr>
		<tr>
			<td>DNA polymerases</td>
			<td></td>
			<td></td>
			<td>we prepare these in our laboratory using published protocols.</td>
		</tr>
	</tbody>
</table>

dna polymerase activity assay using near-infrared fluorescent labeled dna visualized by acrylamide gel electrophoresis

For any enzyme, robust, quantitative methods are required for characterization of both native and engineered enzymes. For DNA polymerases, DNA synthesis can be characterized using an in vitro DNA synthesis assay followed by polyacrylamide gel electrophoresis. The goal of this assay is to quantify synthesis of both natural DNA and modified DNA (M-DNA). These approaches are particularly useful for resolving oligonucleotides with single nucleotide resolution, enabling observation of individual steps during enzymatic oligonucleotide synthesis. These methods have been applied to the evaluation of an array of biochemical and biophysical properties such as the measurement of steady-state rate constants of individual steps of DNA synthesis, the error rate of DNA synthesis, and DNA binding affinity. By using modified components including, but not limited to, modified nucleoside triphosphates (NTP), M-DNA, and/or mutant DNA polymerases, the relative utility of substrate-DNA polymerase pairs can be effectively evaluated. Here, we detail the assay itself, including the changes that must be made to accommodate nontraditional primer DNA labeling strategies such as near-infrared fluorescently labeled DNA. Additionally, we have detailed crucial technical steps for acrylamide gel pouring and running, which can often be technically challenging.

A successful polyacrylamide gel analysis of a qualitative characterization of overall activity (described in section 2.1, Figure 1) and of steady-state kinetics (described in the note at conclusion of section 2.1, Figure 2) are shown. An unsuccessful polyacrylamide gel analysis is also shown (Figure 3).
Note that no commercially available l...

Watch this Scientific Journal Video about DNA Polymerase Activity Assay Using Near-infrared Fluorescent Labeled DNA Visualized by Acrylamide Gel Electrophoresis at JoVE.com

DNA Polymerase Activity Assay Using Near-infrared Fluorescent Labeled DNA Visualized by Acrylamide Gel Electrophoresis

This protocol describes the characterization of DNA polymerase synthesis of modified DNA through observation of changes to near-infrared fluorescently labeled DNA using gel electrophoresis and gel imaging. Acrylamide gels are used for high resolution imaging of the separation of short nucleic acids, which migrate at different rates depending on size.

For any enzyme, robust, quantitative methods are required for characterization of both native and engineered enzymes. For DNA polymerases, DNA synthesis ...

The overall goal of this procedure is to analyze DNA polymerase activity on a single nucleotide level. This method can help answer key questions in the DNA polymerase field such as which specific steps of DNA synthesis are limited by DNA modifications. The main advantage of this technique is that you can observe single nucleotide changes enabling precise observation of polymerase activity.While attempting this procedure it is important to remember to plan ahead. Many of the steps are time-sensitive. To begin this procedure first prepare the buffers, DNA duplex mix and protein dilution as outlined in the text protocol.Next, set the temperature of a dry bath to 50 degrees Celsius. Add 24 microliters of the annealed duplex mix to a microcentrifuge tube containing 25 microliters of 2X dNTPs. After this, transfer 9.8 microliters of this mixture to a microcentrifuge tube containing 20 microliters of quenching buffer orange to prepare the no enzyme control.Then add 0.8 microliters of 50X enzyme to the duplexed dNTP mixture. Use a large volume pipette to thoroughly mix the solution. Incubate in the dry bath.Quench the reaction by removing 10 microliters of each reaction mixture and then adding it to a microcentrifuge tube containing 20 microliters of quenching buffer orange. Prepare the acrylamide mix for gel electrophoresis as outlined in the text protocol. Next, wash two 33-centimeter by 42-centimeter gel plates thoroughly with soap and water.Dry each plate face with paper towels and then use delicate task wipers to dry the remaining areas. Rinse the dried plates with 70%ethanol and wipe each again with task wipers. After this, run a gloved hand under deionized water and then using wetted fingers gently wet some 0.75 millimeter spacers.Place the spacers along the edge of the notched plate. Use task wipers to clean up any water that may have splashed on the plates. Put the plates together and then use gel tape to cover the bottom and sides leaving the top untaped.Make sure the tape is aligned evenly and sealed tightly. Using a razor cut the ends of the tape. Then add an additional layer of tape to the bottom of the gel.After preparing the reagents, acquire a squirt bottle and remove the pointed funnel. Using a graduated cylinder, add 125 milliliters of water. Then use a permanent marker to mark the level of the water on the outside of the bottle.Discard the water. Next set up the cork rings and plate sandwich next to a sink as outlined in the text protocol. Place the empty squirt bottle and the prepared APS and TEMED solutions on the other side of the sink.Place a well comb with the desired number of wells and four clamps nearby. Then add 20%acrylamide gel solution to the squirt bottle until it is at the marked level. Simultaneously add 120 microliters of TEMED and 600 microliters of APS to the polyacrylamide gel solution.Quickly add an additional 600 microliters of APS. Swiftly cap the squirt bottle and mix by swirling. Next place the plate sandwich into the sink.Begin pouring, applying slow and steady pressure to the bottle to ensure the gel solution flows steadily. Pour until the gel has reached the notched area and is slightly overflowing from the notched edge. Tilt the plates to remove any air bubbles.Then add the well comb to the plate sandwich. Place the clamps on the comb such that they press down allowing for even distribution of the wells. Quickly dispose of any remaining gel solution in the squirt bottle to an appropriate waste container.Rinse with the deionized water three times through the squirt nozzle to clean the bottle. To begin remove all binder clips from the plate sandwich. Using a razor, cut and remove the gel tape from the edges.Wipe the glass surfaces with paper towels and water to clean off as much polymerized gel residue as possible. Use a razor along the edges to scrape off any remaining gel. Next push the well comb evenly on both sides to remove it.Using a razor, cut off any excess gel along the top of the plate sandwich. Then slice along the notched edge of the plate. Using a syringe and deionized water, rinse the wells to remove any debris.Make sure that each well can be filled with water and is not blocked by excess polymerized gel. Next place the plate sandwich into the apparatus so that the longer plate is facing outward while the notched space is facing inward. Clip the plate sandwich and aluminum plate together attached to the apparatus.Add additional clips to the outside of the plate to promote even running. Add TBE buffer using just enough to cover the base notches and the wells at the top. Run the gel electrophoresis at 50 watts for 20 minutes to warm the plates.After this use a syringe and TBE buffer to clean the wells. Repeat the syringe wash several times to ensure that all remaining buffer salts have been removed from the wells. Next set up the outermost lanes on each side as outlined in the text protocol.Add three microliters of 95%formamide with bromophenol blue to the appropriate wells of the gel. Load all samples and allow them to settle for one minute. After connecting the apparatus and power source, set the power to between 50 and 55 watts.Run the gel for approximately three hours or until the bromophenol blue dye front has run at least two-thirds of the way down the gel. After this, image the gel as outlined in the text protocol. In this study an assay is developed to characterize the DNA polymerase-mediated synthesis of modified DNA.A successful qualitative characterization of overall activity shows individual bands that are well-defined and regular. Activity is judged by both the length of the products and the portion of the labeled primer that is converted to larger products. As can be seen, E6 and E5 are the most active enzymes, while E4 and E1 are the least active.A quantitative analysis using steady-state kinetics can also be performed using these methods. Because only the N and the N+1 products are synthesized, the singular event can be quantified successfully. The basic methodology here can also be used to study a number of other DNA or RNA modifying enzymes other than polymerases.

dna-polymerase-activity-assay-using-near-infrared-fluorescent-labeled

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Biochemistry

14.0K vues.  W.M. Keck Science Department of Claremont Mckenna, Pitzer, and Scripps College. The overall goal of this procedure is to analyze DNA polymerase activity on a single nucleotide level. This method can help answer key questions in the DNA polymerase field such as which specific steps of DNA synthesis are limited by DNA modifications. The main advantage of this technique is that you can observe single nucleotide changes enabling precise observation of polymerase activity.While attempting this procedure it is important to remember to plan ahead. Many of the steps are t...