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Method Article

Studying DNA Looping by Single-Molecule FRET

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DOI:

10.3791/51667

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June 28th, 2014

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In This Article

Summary

This study presents a detailed experimental procedure to measure looping dynamics of double-stranded DNA using single-molecule Fluorescence Resonance Energy Transfer (FRET). The protocol also describes how to extract the looping probability density called the J factor.

Abstract

Bending of double-stranded DNA (dsDNA) is associated with many important biological processes such as DNA-protein recognition and DNA packaging into nucleosomes. Thermodynamics of dsDNA bending has been studied by a method called cyclization which relies on DNA ligase to covalently join short sticky ends of a dsDNA. However, ligation efficiency can be affected by many factors that are not related to dsDNA looping such as the DNA structure surrounding the joined sticky ends, and ligase can also affect the apparent looping rate through mechanisms such as nonspecific binding. Here, we show how to measure dsDNA looping kinetics without ligase by detecting transient DNA loop formation by FRET (Fluorescence Resonance Energy Transfer). dsDNA molecules are constructed using a simple PCR-based protocol with a FRET pair and a biotin linker. The looping probability density known as the J factor is extracted from the looping rate and the annealing rate between two disconnected sticky ends. By testing two dsDNAs with different intrinsic curvatures, we show that the J factor is sensitive to the intrinsic shape of the dsDNA.

Introduction

Understanding the mechanical properties of dsDNA is of fundamental importance in basic sciences and engineering applications. The structure of dsDNA is more complicated than a straight helical ladder because roll, tilt, and twist angles between successive base pairs can vary with sequence. Thermal fluctuations can cause dsDNA to undergo diverse modes of conformational fluctuations such as bending, twisting and stretching. Transitions such as melting and kinking can also occur in extreme conditions.

Among these motions, dsDNA bending has the most noticeable biological impact1. dsDNA bending is associated with gene repression or ac....

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Protocol

1. dsDNA Sample Preparation

  1. Design globally curved DNAs by repeating a 10-mer sequence. For example, 5’-GTGCCAGCAACAGATAGC - (TTTATCATCCTTTATCATCCX)7 - TTTCATTCGAGCTCGTTGTTG-3’ is a 186-bp curved DNA where X is a random extra base and the sequence flanking the repeating 10-mer sequence are adapter sequences.
    NOTE: In this example two 10-mers with opposite preferences to nucleosome formation based on a large-scale nucleosome occupancy study by Kaplan et al.15 were chosen. Since the helical repeat of dsDNA is close to 10 bp, any net deflection of the helical axis of the 10-mer will accumul....

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Results

DNA molecules used for the looping study consist of a duplex region of variable sequence and length and single-stranded overhangs that are complementary to each other. The overhangs, which are 7-base long, can anneal to each other to capture the looped state. Each overhang contains either Cy3 or Cy5 that is linked in the DNA backbone through amidite chemistry. The Cy5-overhang is also linked with biotin-TEG (15-atom Tetra-Ethylene Glycol spacer) for surface immobilization (see Figure 4A). All these modif.......

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Discussion

A simple single-molecule assay based on FRET was used to study looping kinetics of DNAs of different intrinsic shapes. Curved DNAs can be prepared by repeating a 10-mer sequence in phase with the helical period of 10.5 bp, and their curvatures can be estimated using PAGE. These dsDNAs are designed with sticky ends to allow transient loop stabilization. We extracted the looping rate from the exponential rise in the number of looped molecules over time. The annealing rate constant between the disconnected sticky end segmen.......

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Disclosures

The authors declare no conflicts of interest.

Acknowledgements

We thank James Waters, Gable Wadsworth and Bo Broadwater for critically reading the manuscript. We also thank four anonymous reviewers for providing useful comments. We acknowledge financial support from Georgia Institute of Technology, the Burroughs Wellcome Fund Career Award at the Scientific Interface, and the student research network grant from NSF Physics of Living Systems.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Small DNA FRAG Extract Kit-100PRVWR97060-558
Acrylamide 40% solution 500 mlVWR97064-522
Bis-acrylamide 2% (w/v) solution 500 mlVWR97063-948
GeneRuler 100 bp DNA Ladder, 100-1,000 bpFermentasSM0241
Mini Vertical PAGE SystemVWR89032-300
Syringe filter 0.2 μm CS50VWRA2666
TroloxSigma-Aldrich238813-1Gtriplet state quencher
Protocatechuic acid (PCA)Sigma-Aldrich08992-50MGoxygen scavenging system
Protocatechuate 3,4-Dioxygenase (PCD)Sigma-AldrichP8279-25UNoxygen scavenging system
mPEG-silane, MW 2,000 1 gLaysan BioMPEG-SIL-2000-1g
Biotin-PEG-Silane, MW 3,400Laysan BioBiotin-PEG-SIL-3400-1g
Avidin, NeutrAvidin Biotin-binding ProteinInvitrogenA2666
Phusion Hot Start High-Fidelity DNA PolymeraseNew England BiolabsF-540L
Gel/PCR DNA Fragments Extraction KitIBI ScientificIB47020
Premium plain glass microscope slidesFisher Scientific12-544-1
VWR micro cover glass, rectangular, no. 1VWR48404-456
Fisher Scientific Isotemp 1006S Recirculating Chiller/HeaterFisher Scientifictemperature control
Objective Cooling CollarBioptechs150303temperature control
KMI53 Biological Micrometer Measuring StageSemprexKMI53
High Performance DPSS Laser 532 nm 50 mWEdmund opticsNT66-968Cy3 excitation
CUBE Fiber Pigtailed 640 nm, 30 mW, Fiber, FC/APC ConnectorCoherent1139604Cy5 excitation
650 nm BrightLine Dichroic BeamsplitterSemrockFF650-Di01-25x36splitting dichroic
LaserMUX Beam Combiner, reflects 514.5, 532, & 543.5 nm lasers, 25 mmSemrockLM01-552-25combining dichroic
Brightline Fluorescence Filter 593/40SemrockFF01-593/40-25Cy3 emission filter
635 nm EdgeBasic LWP longpass Filter, 25 mmSemrockBLP01-635R-25Cy5 emission filter
EMCCD iXon+Andor TechnologyDU-897E-CS0-#BV
IX51 inverted microscope frameOlympus
Objective UApo N 100X/1.49 Oil TIRFOlympus
Immersion oil type-F for fluorescence microscopyOlympusIMMOIL-F30CC
2 mm Diameter 45° Rod Lens Aluminum Coated Edmund optics54-092miniature mirror
1/4" Travel Single-Axis Translation StageThorlabsMS-1translation of miniature mirror
Ø1" Achromatic Doublet, ARC: 400-700 nm, f=200 mmThorlabsAC254-200-Afocusing lens
Adjustable Mechanical SlitThorlabsVA100
Dielectric MirrorThorlabsBB1-E02
Ø1" Achromatic Doublet, f = 100 mmThorlabsAC254-100-Arelay lens
Lens Mount for Ø1" OpticsThorlabsLMR1
Dichroic Filter MountThorlabsFFM1
Fixed Cage Cube PlatformThorlabsB3C
Kinematic Mount for Ø1" OpticsThorlabsKM100
N-BK7 Plano-Convex Lens, Ø1", f = 40 mmThorlabsLA1422-Acollimating lens
N-BK7 Plano-Convex Lense, Ø6.0 mm, f = 15 mmThorlabsLA1222-Atelescope lens
N-BK7 Plano-Convex Lense, Ø6.0 mm, f = 150 mmThorlabsLA1433-Atelescope lens

References

  1. Garcia, H. G., et al. Biological consequences of tightly bent DNA: The other life of a macromolecular celebrity. Biopolymers. 85, 115-130 (2007).
  2. Wiggins, P. A., et al. High flexibility of DNA on short length scales prob....

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