Evidence map›Paper›PMID 21491127›Full record

ArticleJournal of computational neuroscience2011

Sequestration of CaMKII in dendritic spines in silico.

Shahid Khan, Yixiao Zou, Asma Amjad, Ailia Gardezi, Carolyn L Smith, Christine Winters, Thomas S Reese

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of computational neuroscience, 2011. 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
1.2field-weighted citation impact, top 27% 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, 29 citations in OpenAlex.

  1. Article
  2. Synaptic memory and CaMKII.Physiological reviews · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Spatially extended hybrid methods: a review.Journal of the Royal Society, Interface · 2018
    Review
  10. Article
  11. Article
  12. Multiple spatial and kinetic subpopulations of CaMKII in spines and dendrites as resolved by single-molecule tracking PALM.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  13. Article
  14. Review
  15. Superresolving dendritic spines.Biophysical journal · 2013
    Article
  16. Article
  17. Spatiotemporal maps of CaMKII in dendritic spines.Journal of computational neuroscience · 2012
    Article
  18. Article
  19. Review
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

7 authors at 2 institutions in 2 countries.

Shahid KhanLaboratory of Neurobiology, National Institute of Neurological Diseases & Stroke, Bethesda, MD 20892, USA. ShahidKhan@mbclss.org
Yixiao Zou
Asma Amjad
Ailia Gardezi
Carolyn L Smith
Christine Winters
Thomas S Reese
National Institute of Neurological Disorders and Stroke · USLahore University of Management Sciences · PK

Funding

Macromolecular Architecture Of The SynapseZIANS002972 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI REESE, THOMAS S · 2009 to 2025
$25.6M
Dynamic Structural Properties of SynapsesZIANS003113 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI REESE, THOMAS S · 2009 to 2025
$16.0M
BACTERIAL CHEMOTAXIS PROBED BY PHOTORELEASED LIGANDSR01GM049319 · NIGMS · YESHIVA UNIVERSITY · PI KHAN, SHAHID M · 1996 to 2003
$852k
NIGMS NIH HHS R01-GM49319
6 · The paper itself

Abstract

Calcium calmodulin dependent kinase II (CaMKII) is sequestered in dendritic spines within seconds upon synaptic stimulation. The program Smoldyn was used to develop scenarios of single molecule CaMKII diffusion and binding in virtual dendritic spines. We first validated simulation of diffusion as a function of spine morphology. Additional cellular structures were then incorporated to simulate binding of CaMKII to the post-synaptic density (PSD); binding to cytoskeleton; or their self-aggregation. The distributions of GFP tagged native and mutant constructs in dissociated hippocampal neurons were measured to guide quantitative analysis. Intra-spine viscosity was estimated from fluorescence recovery after photo-bleach (FRAP) of red fluorescent protein. Intra-spine mobility of the GFP-CaMKIIα constructs was measured, with hundred-millisecond or better time resolution, from FRAP of distal spine tips in conjunction with fluorescence loss (FLIP) from proximal regions. Different FRAP \ FLIP profiles were predicted from our Scenarios and provided a means to differentiate binding to the PSDs from self-aggregation. The predictions were validated by experiments. Simulated fits of the Scenarios provided estimates of binding and rate constants. We utilized these values to assess the role of self-aggregation during the initial response of native CaMKII holoenzymes to stimulation. The computations revealed that self-aggregation could provide a concentration-dependent switch to amplify CaMKII sequestration and regulate its activity depending on its occupancy of the actin cytoskeleton.

Indexed as

Models, NeurologicalActinsAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2Chlorocebus aethiopsCOS CellsCytoskeletonDendritic SpinesPrimary Cell CultureProtein BindingProtein TransportRatsRats, Sprague-DawleySynaptic TransmissionActinsCalcium-Calmodulin-Dependent Protein Kinase Type 2

Identifiers

PMID21491127
OpenAlexW1994069838

What OpenQuestion holds

Textmetadata
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.