Evidence map›Paper›PMID 21094684›Full record

ReviewJournal of structural biology2011

Exploring the spatial and temporal organization of a cell's proteome.

Martin Beck, Maya Topf, Zachary Frazier, Harianto Tjong, Min Xu, Shihua Zhang, Frank Alber

Abstract readReview
In one paragraph

Review in Journal of structural biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
7.8field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Whole-Cell Models and Simulations in Molecular Detail.Annual review of cell and developmental biology · 2019
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. A computational approach to increase time scales in Brownian dynamics-based reaction-diffusion modeling.Journal of computational biology : a journal of computational molecular cell biology · 2012
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Gradient-based high precision alignment of cryo-electron subtomograms.IEEE International Conference on Systems Biology : [proceedings]. IEEE International Conference on Systems Biology · 2011
    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

7 authors at 3 institutions in 3 countries.

Martin BeckEuropean Molecular Biology Laboratory, Meyerhofstr. 1, 69117 Heidelberg, Germany.
Maya Topf
Zachary Frazier
Harianto Tjong
Min Xu
Shihua Zhang
Frank Alber
University of Southern California · USBirkbeck, University of London · GBEuropean Molecular Biology Laboratory · DE

Funding

NEW TOOLS FOR EXPLORING THE DYNAMIC INTERACTOME(RMI)U54RR022220 · NCRR · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2005 to 2011
$19.3M
New Tools for Exploring the Dynamic Interactome (Renewal)U54GM103511 · NIGMS · ROCKEFELLER UNIVERSITY · PI ROUT, MICHAEL P · 2012 to 2013
$6.2M
Computational Methods Towards the Spatio-Temporal Organization of the ProteomeR01GM096089 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ALBER, FRANK · 2011 to 2015
$1.6M
Medical Research Council G0600084NCRR NIH HHS 2U54RR022220-06NCRR NIH HHS U54 RR022220NIGMS NIH HHS 1R01GM096089NIGMS NIH HHS R01 GM096089NIGMS NIH HHS U54 GM103511
6 · The paper itself

Abstract

To increase our current understanding of cellular processes, such as cell signaling and division, knowledge is needed about the spatial and temporal organization of the proteome at different organizational levels. These levels cover a wide range of length and time scales: from the atomic structures of macromolecules for inferring their molecular function, to the quantitative description of their abundance, and spatial distribution in the cell. Emerging new experimental technologies are greatly increasing the availability of such spatial information on the molecular organization in living cells. This review addresses three fields that have significantly contributed to our understanding of the proteome's spatial and temporal organization: first, methods for the structure determination of individual macromolecular assemblies, specifically the fitting of atomic structures into density maps generated from electron microscopy techniques; second, research that visualizes the spatial distributions of these complexes within the cellular context using cryo electron tomography techniques combined with computational image processing; and third, methods for the spatial modeling of the dynamic organization of the proteome, specifically those methods for simulating reaction and diffusion of proteins and complexes in crowded intracellular fluids. The long-term goal is to integrate the varied data about a proteome's organization into a spatially explicit, predictive model of cellular processes.

Indexed as

AlgorithmsCryoelectron MicroscopyElectron Microscope TomographyImage Processing, Computer-AssistedModels, MolecularProtein ConformationProteinsProteomeProteomicsProteinsProteome

Identifiers

PMID21094684
PMCPMC3784337
OpenAlexW2125465188

What OpenQuestion holds

Textmetadata
LicenceTDM
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.