Method Article

Single-Molecule Dwell-Time Analysis of Restriction Endonuclease-Mediated DNA Cleavage

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DOI:

10.3791/62112

February 7th, 2021

In This Article

Summary

Using quantum-dot-labeled DNA and total internal reflection fluorescence microscopy, we can investigate the reaction mechanism of restriction endonucleases while using unlabeled protein. This single-molecule technique allows for massively multiplexed observation of individual protein-DNA interactions, and data can be pooled to generate well-populated dwell-time distributions.

Abstract

This novel total internal reflection fluorescence microscopy-based assay facilitates the simultaneous measurement of the length of the catalytic cycle for hundreds of individual restriction endonuclease (REase) molecules in one experiment. This assay does not require protein labeling and can be carried out with a single imaging channel. In addition, the results of multiple individual experiments can be pooled to generate well-populated dwell-time distributions. Analysis of the resulting dwell-time distributions can help elucidate the DNA cleavage mechanism by revealing the presence of kinetic steps that cannot be directly observed. Example data collected using this assay with the well-studied REase, EcoRV - a dimeric Type IIP restriction endonuclease that cleaves the palindromic sequence GAT↓ATC (where ↓ is the cut site) - are in agreement with prior studies. These results suggest that there are at least three steps in the pathway to DNA cleavage that is initiated by introducing magnesium after EcoRV binds DNA in its absence, with an average rate of 0.17 s-1 for each step.

Introduction

Restriction endonucleases (REases) are enzymes that effect sequence-specific double-strand breaks in DNA. The discovery of REases in the 1970s led to the development of recombinant DNA technology, and these enzymes are now indispensable laboratory tools for genetic modification and manipulation1. Type II REases are the most widely used enzymes in this class as they cleave DNA at a fixed location either within or near their recognition sequence. However, there is a great deal of variation among the Type II REases, and they are divided into several subtypes based on particular enzymatic properties rather than being classified according to their e....

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Protocol

1. General information

  1. Oligonucleotide design
    NOTE: The 60 base-pair (bp)-long DNA substrate is formed from a pair of complementary oligonucleotides with a duplex melting temperature of 75 °C in 100 mM NaCl.
    1. Order one oligonucleotide synthesized with a single 5' biotin modification and the other with a 5' thiol modification (with a six-carbon spacer). Place the recognition site in the center of the duplex region.
      NOTE: The oligonucleotide sequences for use with EcoRV are shown below (recognition site in bold).
      5' biotin - AAA ACC GAC ATG TTG ATT TCC TGA AAC GGG ATA TCA TCA AAG CCA TG....

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Results

The flow cell is directly coupled to a high numerical aperture oil-immersion 60x magnification objective on an inverted microscope equipped with laser illumination for through-objective TIRF imaging (Figure 5A). After introducing the DNA substrate and washing away excess DNA and quantum dots, there are typically thousands of individual quantum dots in a field of view (Figure 5B). These quantum dots are stably attached to the glass surface, and they do not underg.......

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Discussion

The DNA substrate for this assay is labeled with a quantum dot using a two-step reaction scheme using sulfo-SMCC. This bifunctional crosslinker consists of an NHS ester moiety that can react with a primary amine, and a maleimide moiety that can react with a sulfhydryl group20. The thiolated oligonucleotides used to prepare the substrate are shipped in their oxidized form. It is important to reduce and purify them, as described, before proceeding with the coupling procedure, or the efficiency of th.......

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Disclosures

The authors have no competing financial interests or other conflicts of interest

Acknowledgements

This work was supported by Award Number K12GM074869 to CME from the National Institute of General Medical Sciences. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of General Medical Sciences or the National Institutes of Health.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
3-aminopropyltriethoxysilane (APTS)Sigma Aldrich440140-100MLStore in dessicator box
5 Minute EpoxyDevcon20845use for sealing the microfluidic device
acetonePharmco329000ACSuse for cleaning coverslips
bath sonicatorFisher ScientificCPXH Model 2800catalog number 15-337-410
Beaker, glass, 100 mL
Benchtop centrifuge
Biotin-PEG-Succinimidyl Valerate (MW 5,000)Laysan BioBIO-SVA-5KSuccinimidyl valerate has a longer half-life than succinimidyl carbonate
biotinylated oligonucleotideIntegrated DNA Technologiescustom - see protocol for design considerationsRequest 5' Biotin modification and HPLC purification
Bovine Serum Albumin (BSA)VWR0903-5Gprepare a 10 mg/mL solution (aq) and heat to 95 °C before using
Centri-Spin-10 Size Exclusion Spin ColumnsPrinceton SeparationsCS-100 or CS-101used to purify thiolated oligonucleotides after reducing the disulfide bond
Centrifuge tubes 1.5. mL
Coverslips, 1-inch square glass
coverslip holders
diamond point wheelDremel7134use for drilling holes in quartz flow cell topper
dithiothreitol (DTT)Thermo ScientificA39255No-Weigh Format, 7.7 mg/vial
drill press rotary tool workstation standDremel220-01facilitates quartz drilling
EcoRV (REase used to generate example data)New England BiolabsR0195T or R0195MUse 100,000 units/mL stock to avoid adding excess glycerol Check REBASE for suppliers of other REases
ethanolvariousCAS 64-17-5denatured or 95% are acceptable, use for cleaning coverslips
Ethylenediaminetetraacetic acid (EDTA)Sigma AldrichEDSBioUltra, anhydrous, store in dessicator box
Flea Micro SpinbarFisherbrand14-513-653 mm x 10 mm size to fit beneath coverslip rack
fluoresceinAcros Organics17324use to make experimental buffers
gravity convection ovenBinder9010-0131
handheld rotary multitoolDremel8220use for drilling holes in quartz flow cell topper
ImagEM X2 EM-CCD CameraHamamatsuC9100-23Bair cooling is adequate for this experiment, use HCImage software or similar to control
Imaging spacer, double-sided, adhesive
Jar, glass with screw cap, (approximately 50 mm diameter by 50 mm high)
magnesium chloride hexahydrateFisher BioreagentsBP214-500use to make experimental buffer with magnesium
MATLAB softwareData analysis
metal tweezersFisher Brand16-100-110
methoxy-PEG-Succinimidyl Valerate (MW 5,000)Laysan BioM-SVA-5KBoth PEGs should have the same NHS ester so that the rate of reaction is consistent
microcentrifugeEppendorf5424
multiposition magnetic stirrerVWR12621-022
N-cyclohexyl-2-aminoethanesulfonic acid (CHES)Acros OrganicsAC20818CAS 103-47-9, use to make CHES buffer
orbital shaker and heater for microcentrifuge tubesQ Instruments1808-0506with 1808-1061 adaptor for 24 x 2.0 mL or 15 x 0.5 mL tubes
Parafilm
PE60 Polyethylene tubing (inner diameter 0.76 mm, outer diameter 1.22 mm)Intramedic625891722 G blunt needles are a good fit for this tubing size
Phosphate-Buffered Saline (PBS) 10xSigma AldrichP7059Use at 1x strength
potassium hydroxideVWR Chemicals BDHBDH9262use a 1 M solution to clean coverslips
Qdot 655 ITK Amino (PEG) Quantum DotsInvitrogenQ21521MP
Quartz Slide, 1 inch square, 1 mm thickElectron Microscopy Sciences72250-10holes must be drilled in the corners for inlet and outlet tubing insertion
reinforced plastic tweezersRubisK35ause for handling coverslips and building microfluidic device
SecureSeal Adhesive SheetsGrace BiolabsSA-S-1Lcut to form spacer for microfluidic device
Single channel syringe pump for microfluidicsNew Era Pump SystemsNE-1002X-USfitted with a 50 mL syringe and a 22 G blunt needle
Slide-a-Lyzer MINI Dialysis Devices, 10 kDa MWCO, 0.1 mLThermo Scientific69570 or 69572used for buffer exchange during quantum dot coupling to DNA
sodium bicarbonateEMD MilliporeSX0320use to make buffer for surface functionalization; 100 mM, pH 8
sodium chlorideMacron7581-12use to make experimental buffers
Sodium phosphate dibasic solution (BioUltra, 0.5 M in water)Sigma Aldrich94046use to make 100 mM sodium phosphate buffer
Sodium phosphate monobasic solution (BioUltra, 5M in water)Sigma Aldrich74092use to adjust pH of 100 mM sodium phosphate buffer
Streptavidin from Streptomyces avidiniiSigma AldrichS4762dissolve at 1 mg/mL and store 25 mL aliqouts at -20 ?
Sulfosuccinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate (sulfo-SMCC)Thermo ScientificA39268No-Weigh Format, 2 mg/vial
Syringe fitted with blunt 21 G needle
Syringe pump
thiolated oligonucleotideIntegrated DNA Technologiescustom - see protocol for design considerationsRequest 5' Thiol Modifier C6 S-S and HPLC purificaiton
TIRF imaging system with 488 nm laser illuminationvariouscustom built
Tris -HClResearch Products InternationalT60050use to make experimental buffers
Tris baseJT Baker4101use to make experimental buffers
Tween-20SigmaP7949use to make blocking buffer
Ultrapure water
vortex mixerVWR10153-842
Wash-N-Dry Coverslip RackElectron Microscopy Sciences70366-16used for surface functionalization of coverslips

References

  1. Roberts, R. J. How restriction enzymes became the workhorses of molecular biology. Proceedings of the National Academy of Sciences of the United States of America. 102 (17), 5905-5908 (2005).
  2. Loenen, W. A., Dryden, D. T., Raleigh, E. A., Wilson, G. G., Murray, N. E.

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Tags

Single Molecule AnalysisTotal Internal ReflectionFluorescence MicroscopyEcoRV EndonucleaseQuantum Dot LabelingMicrofluidic DeviceCatalytic Cycle Measurement

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