Evidence map›Paper›PMID 35352962›Full record

ArticleMolecular biology of the cell2022

Fast and parallel nanoscale three-dimensional tracking of heterogeneous mammalian chromatin dynamics.

Anna-Karin Gustavsson, Rajarshi P Ghosh, Petar N Petrov, Jan T Liphardt, W E Moerner

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  15. Article
  16. Review
  17. Recent Advances in Single-Molecule Tracking and Imaging Techniques.Annual review of analytical chemistry (Palo Alto, Calif.) · 2023
    Review
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Anna-Karin GustavssonDepartment of Chemistry, Stanford University, Stanford, CA 94305.
Rajarshi P GhoshBioengineering, Stanford University, Stanford, CA 94305.
Petar N PetrovDepartment of Chemistry, Stanford University, Stanford, CA 94305.
Jan T LiphardtBioengineering, Stanford University, Stanford, CA 94305.
W E MoernerDepartment of Chemistry, Stanford University, Stanford, CA 94305.
Stanford University · USHoward Hughes Medical Institute · USRice University · USUniversity of California, Berkeley · US

Funding

Single-Molecule Imaging for Cell Biology and Super-Resolution MicroscopyR35GM118067 · NIGMS · STANFORD UNIVERSITY · PI MOERNER, WILLIAM E · 2016 to 2025
$6.2M
Deep Super-localization Microscopy and Effectively Unbleachable Labeling for 4D NucleomicsU01EB021237 · NIBIB · STANFORD UNIVERSITY · PI LIPHARDT, JAN T. · 2015 to 2017
$1.1M
Three-dimensional super-resolution imaging and tracking of disease and treatment mechanisms of progeriaR00GM134187 · NIGMS · RICE UNIVERSITY · PI GUSTAVSSON, ANNA KARIN EVA · 2021 to 2023
$747k
NIBIB NIH HHS U01 EB021237NIGMS NIH HHS R00 GM134187NIGMS NIH HHS R35 GM118067
6 · The paper itself

Abstract

Chromatin organization and dynamics are critical for gene regulation. In this work we present a methodology for fast and parallel three-dimensional (3D) tracking of multiple chromosomal loci of choice over many thousands of frames on various timescales. We achieved this by developing and combining fluorogenic and replenishable nanobody arrays, engineered point spread functions, and light sheet illumination. The result is gentle live-cell 3D tracking with excellent spatiotemporal resolution throughout the mammalian cell nucleus. Correction for both sample drift and nuclear translation facilitated accurate long-term tracking of the chromatin dynamics. We demonstrate tracking both of fast dynamics (50 Hz) and over timescales extending to several hours, and we find both large heterogeneity between cells and apparent anisotropy in the dynamics in the axial direction. We further quantify the effect of inhibiting actin polymerization on the dynamics and find an overall increase in both the apparent diffusion coefficient D* and anomalous diffusion exponent α and a transition to more-isotropic dynamics in 3D after such treatment. We think that in the future our methodology will allow researchers to obtain a better fundamental understanding of chromatin dynamics and how it is altered during disease progression and after perturbations of cellular function.

Indexed as

ChromatinChromosomesAnimalsAnisotropyDiffusionGene Expression RegulationMammalsChromatin

Identifiers

PMID35352962
PMCPMC9265149
OpenAlexW4226034442

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.