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Conserved Binding Sites01:49

Conserved Binding Sites

Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
Conserved Binding Sites01:49

Conserved Binding Sites

Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
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...
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form dimers that...
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...
Physiological Pharmacokinetic Models: Assumption with Protein Binding01:13

Physiological Pharmacokinetic Models: Assumption with Protein Binding

Physiological models with protein binding in pharmacokinetics offer a sophisticated approach to understanding drug disposition. These models consider drug-protein interactions, enabling them to effectively predict drug concentrations in different organs and tissues. This precision aids in accurate drug dosing, providing a significant advantage over conventional models. A key process within these models is equilibration, which ensures that drug concentrations achieve a steady state within the...

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Related Experiment Video

Updated: Jun 1, 2026

Single-Molecule Measurement of Protein Interaction Dynamics Within Biomolecular Condensates
06:48

Single-Molecule Measurement of Protein Interaction Dynamics Within Biomolecular Condensates

Published on: January 5, 2024

Discrete persistent-chain model for protein binding on DNA.

Pui-Man Lam1, Yi Zhen

  • 1Physics Department, Southern University, Baton Rouge, Louisiana 70813, USA. puiman_lam@subr.edu

Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|May 24, 2011
PubMed
Summary
This summary is machine-generated.

We developed a model for protein binding on DNA, calculating how force affects binding and DNA extension. This helps analyze experimental data to understand protein-DNA interactions.

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Last Updated: Jun 1, 2026

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Published on: January 5, 2024

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Area of Science:

  • Biophysics
  • Molecular Biology
  • Computational Biology

Background:

  • Protein-DNA interactions are crucial for biological processes.
  • Understanding these interactions at a molecular level is essential.
  • Quantifying binding dynamics under force is experimentally challenging.

Purpose of the Study:

  • To develop a discrete persistent-chain model for protein binding on DNA.
  • To derive analytical and numerical solutions for force-extension curves.
  • To provide a method for analyzing experimental data and deducing binding parameters.

Main Methods:

  • Developed a discrete persistent-chain model incorporating protein binding sites and energy costs.
  • Derived analytic expressions for force-extension curves and protein fraction at low forces.
  • Employed numerical methods to solve the model for higher forces.

Main Results:

  • Obtained analytic solutions for force-extension curves and bound protein fractions under small forces.
  • Achieved numerical solutions for force-extension curves and average bound protein fractions at higher forces.
  • The model successfully relates applied force to DNA extension and binding status.

Conclusions:

  • The developed model provides a framework for understanding protein-DNA binding under mechanical force.
  • It enables the analysis of experimental force-extension curves.
  • The model can deduce the number of bound proteins, particularly in cases of non-specific binding.