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Related Concept Videos

Labeling DNA Probes03:31

Labeling DNA Probes

DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
DNA as a Genetic Template02:05

DNA as a Genetic Template

Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
DNA Packaging00:58

DNA Packaging

Overview
The DNA Replication Fork01:02

The DNA Replication Fork

An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication forks, one in...
DNA Topoisomerases02:02

DNA Topoisomerases

Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types.  Type I...

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Related Experiment Video

Updated: May 11, 2026

Studying DNA Looping by Single-Molecule FRET
11:27

Studying DNA Looping by Single-Molecule FRET

Published on: June 28, 2014

Measuring shape-dependent looping probability of DNA.

Tung T Le1, Harold D Kim

  • 1School of Physics, Georgia Institute of Technology, Atlanta, Georgia, USA.

Biophysical Journal
|May 14, 2013
PubMed
Summary

Short DNA loops form faster than predicted, suggesting current models don't fully capture DNA's intrinsic shape and its effect on looping dynamics.

Area of Science:

  • Molecular Biology
  • Biophysics
  • Structural Biology

Background:

  • Short DNA loops form more readily than predicted by the wormlike chain model.
  • The intrinsic curvature of double-stranded DNA (dsDNA) can significantly impact looping dynamics but is often overlooked.
  • Previous experiments did not fully account for dsDNA's inherent shape.

Purpose of the Study:

  • To investigate how the intrinsic shape of dsDNA influences its looping dynamics.
  • To characterize the shapes of synthetic dsDNA molecules with varying sequences but equal lengths.
  • To compare measured looping rates with theoretical predictions based on DNA shape.

Main Methods:

  • Gel electrophoresis was used to characterize the shapes of synthetic dsDNA molecules.
  • Förster resonance energy transfer (FRET)-based assays measured DNA looping rates.

Related Experiment Videos

Last Updated: May 11, 2026

Studying DNA Looping by Single-Molecule FRET
11:27

Studying DNA Looping by Single-Molecule FRET

Published on: June 28, 2014

  • The J factor (jM), a measure of looping probability, was extracted from experimental data.
  • Dinucleotide angular parameters derived from gel mobility were used to predict jM via the wormlike chain model.
  • Main Results:

    • A strong correlation was observed between DNA curvature and the measured J factor (jM).
    • Measured jM values were consistently higher than predictions from most dinucleotide models.
    • Discrepancies suggest limitations in reconciling looping probability with gel mobility using the wormlike chain model.

    Conclusions:

    • The intrinsic shape of dsDNA is crucial for accurately analyzing looping dynamics.
    • Current models struggle to reconcile observed looping probabilities with DNA shape data derived from gel electrophoresis.
    • Further research is needed to integrate intrinsic DNA shape into theoretical models of DNA looping.