Related Experiment Video
Updated: Sep 18, 2025

Author Spotlight: Exploring Intrinsically Disordered Protein Dynamics Through NMR Relaxation Experiments
Published on: November 1, 2024
Long-Range Water Ordering between Intrinsically Disordered Proteins and Its Impact on Protein Diffusion.
Hongli Li1, Binming Han1, Moxin Zhang1
1Zhejiang Province Key Laboratory of Quantum Technology and Device, School of Physics, Zhejiang University, Zheda Road 38, Hangzhou 310027, China.
Intrinsically disordered proteins (IDPs) enhance water structuring and slow diffusion between them, even without direct contact. This water ordering increases effective viscosity, impacting IDP behavior in cellular condensates.
Area of Science:
- Biophysics
- Molecular Biology
- Soft Matter Physics
Background:
- Intrinsically disordered proteins (IDPs) are crucial for forming membraneless organelles.
- IDP diffusion dynamics influence condensate stability, phase separation, and molecular recognition.
Purpose of the Study:
- To investigate the diffusion dynamics of LAF-1 RGG domains.
- To explore the interplay between IDPs and their solvent environment.
Main Methods:
- Molecular dynamics simulations were used.
- Diffusion dynamics of IDPs and water molecules were analyzed.
Main Results:
- IDPs significantly enhance structural ordering of water molecules between them.
- This ordering slows down water diffusion, creating an effect similar to an 18 K solvent cooling.
- Increased effective viscosity around IDPs hinders their diffusion, even without interchain contacts.
Conclusions:
- IDPs profoundly influence the surrounding water structure and dynamics.
- The observed water ordering and diffusion slowdown contribute to increased effective viscosity, impacting IDP behavior.
- These findings offer insights into the physical mechanisms governing membraneless organelle formation and function.
More Related Videos
08:48High-Resolution Neutron Spectroscopy to Study Picosecond-Nanosecond Dynamics of Proteins and Hydration Water
Published on: April 28, 2022
09:17Structure-Based Simulation and Sampling of Transcription Factor Protein Movements along DNA from Atomic-Scale Stepping to Coarse-Grained Diffusion
Published on: March 1, 2022
Related Concept Videos
Protein Diffusion in the Membrane
Intrinsically Disordered Proteins
Protein Folding
Aquaporins
Noncovalent Attractions in Biomolecules
Four types of noncovalent interactions are hydrogen bonds, van der Waals forces, ionic bonds, and hydrophobic interactions.
Hydrogen bonding results from the electrostatic attraction of a hydrogen atom covalently bonded to a strong-electronegative atom like oxygen,...
Ligand Binding Sites
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...