Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Multiple diffusion mechanisms due to nanostructuring in crowded environments.

Hugo Sanabria1, Yoshihisa Kubota, M Neal Waxham

  • 1Department of Neurobiology and Anatomy, University of Texas Health Science Center at Houston, Houston, Texas 77030, USA. hugo.sanabria@uth.tmc.edu

Biophysical Journal
|October 17, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Multidomain Coupling Governs FoxP1 Assembly and Nuclear Compartmentalization.

bioRxiv : the preprint server for biology·2026
Same author

Time heterogeneity of the Förster radius from dipole orientational dynamics impacts single-molecule Förster resonance energy transfer experiments.

Physical review research·2026
Same author

Chiral Polar Eu<sub>2</sub>(SeO<sub>3</sub>)<sub>2</sub>(SO<sub>4</sub>)(H<sub>2</sub>O)<sub>2</sub>: A Pathway Toward Narrow Optical Line Widths and Microsecond Lifetimes for Quantum Memory Candidates.

Journal of the American Chemical Society·2026
Same author

PP2A and CDK16 antagonistically regulate WIPI2B phosphorylation and neuronal autophagosome biogenesis.

bioRxiv : the preprint server for biology·2026
Same author

Investigating the Cytoskeleton of DRGs Using Cryo-Electron Microscopy and Deep Learning.

Cytoskeleton (Hoboken, N.J.)·2026
Same author

Nanodomain formation in lipid bilayers II: The influence of mixed-chain saturated lipids.

Biochimica et biophysica acta. Biomembranes·2026
Same journal

Quantifying the Peripheral Surface Information Entropy from Conformational Ensembles of Globular Protein-Peptide Complexes.

Biophysical journal·2026
Same journal

Anisotropic unbinding and location-dependent hovering of a kinesin motor head over microtubule.

Biophysical journal·2026
Same journal

Kinesin-5/Cut7 C-terminal tail phosphorylation influence on motor regulation through multi-scale molecular modeling.

Biophysical journal·2026
Same journal

Dynamic conformations of fluorophores on self-labeling protein tags.

Biophysical journal·2026
Same journal

Different actions of RyR2 open and closed channel block explained by a multiscale Ca<sup>2+</sup> release model.

Biophysical journal·2026
Same journal

Membrane Environment Sets the Functional pK<sub>a</sub> of Ionizable Lipids.

Biophysical journal·2026
See all related articles

Intracellular diffusion is hindered by immobile barriers and molecular crowding, leading to anomalous subdiffusion. Advanced analysis revealed distinct diffusion mechanisms and environmental heterogeneity not seen with standard models.

Area of Science:

  • Biophysics
  • Physical Chemistry
  • Materials Science

Background:

  • Intracellular diffusion is crucial for cellular processes.
  • Molecular mobility is often hindered by environmental factors like barriers and crowding.
  • Understanding these hindrances is key to comprehending molecular transport within cells.

Purpose of the Study:

  • To investigate how immobile barriers and molecular crowding affect translational mobility.
  • To compare the efficacy of the maximum entropy method (MEM) with standard anomalous diffusion models for analyzing diffusion data.
  • To explore novel diffusion mechanisms and environmental heterogeneity using advanced analytical techniques.

Main Methods:

  • Multi-photon fluorescence correlation spectroscopy (MP-FCS) was employed to study molecular diffusion.

Related Experiment Videos

  • Immobile barriers were simulated using sol-gel silica nanostructures.
  • Molecular crowding was investigated using varying concentrations of dextran solutions.
  • Data analysis involved both standard anomalous diffusion models and the maximum entropy method.
  • Main Results:

    • Diffusion in both sol-gels and dextran solutions exhibited anomalous subdiffusion.
    • The maximum entropy method identified distinct diffusion mechanisms missed by standard models.
    • These mechanisms are likely related to nanostructuring and the size of crowding agents relative to tracers.
    • MEM analysis provided insights into the heterogeneity of the diffusive environment.

    Conclusions:

    • Immobile barriers and molecular crowding significantly hinder intracellular diffusion, causing anomalous subdiffusion.
    • The maximum entropy method offers a more sensitive approach to uncovering complex diffusion behaviors and environmental heterogeneity.
    • This study advances our understanding of molecular transport in complex biological and synthetic environments.