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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...
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Related Experiment Video

Updated: Jul 19, 2026

In Vitro Chemical Mapping of G-Quadruplex DNA Structures by Bis-3-Chloropiperidines
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In Vitro Chemical Mapping of G-Quadruplex DNA Structures by Bis-3-Chloropiperidines

Published on: May 12, 2023

Biphasic transitions of a hairpin hexanucleotide triplex DNA.

I Lee1, W Deng, L Yang

  • 1Institute of Chemistry, The Chinese Academy of Sciences, Beijing 100080, P.R. China.

Biophysical Chemistry
|October 13, 2006
PubMed
Summary

This study characterizes hairpin triple helix stability using UV spectroscopy, revealing distinct thermodynamic properties for helix-coil transitions. The findings provide insights into DNA triplex stability and conformational changes.

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Area of Science:

  • Biophysical Chemistry
  • Molecular Biology
  • Nucleic Acid Chemistry

Background:

  • DNA triplexes are three-stranded nucleic acid structures with potential applications in gene targeting and therapeutics.
  • Understanding the stability and conformational transitions of these structures is crucial for their effective use.
  • Hairpin triple helices represent a specific structural motif with unique stability characteristics.

Purpose of the Study:

  • To characterize the conformational transitions (helix-coil transitions) of three distinct hairpin triple helix models.
  • To determine the thermodynamic parameters governing the melting of these triplexes and their corresponding duplex forms.
  • To analyze the electrostatic effects influencing the stability of these DNA conformations.

Main Methods:

  • UV spectroscopy was employed to monitor the melting profiles of the hairpin triple helices.
  • Biphasic melting curves were analyzed to obtain thermodynamic parameters such as melting temperature (T(m)) and enthalpy (DeltaH(vH)).
  • The nearest-neighbor Ising model was utilized to analyze the distinct transitions from triplex to duplex and duplex to single strands.

Main Results:

  • The study determined specific thermodynamic properties for three hairpin triple helices (CY, YC, YY) and their duplex counterparts at pH 4.4.
  • Melting temperatures for hairpin triplexes ranged from 19.45 to 28.47 °C, with enthalpies between 234.68 and 293.12 kJ/mol.
  • Duplex forms exhibited higher melting temperatures (30.50 to 33.24 °C) and enthalpies (329.67 to 427.09 kJ/mol), indicating greater stability.

Conclusions:

  • Hairpin triple helices display distinct biphasic melting transitions, allowing for the characterization of their thermodynamic stability.
  • The stability of the triplex and duplex forms is sequence-dependent and influenced by electrostatic interactions.
  • These findings contribute to a deeper understanding of DNA triplex thermodynamics and conformational dynamics.