Evidence map›Paper›PMID 17098795›Full record

ArticleBiophysical journal2007

Compartment-specific feedback loop and regulated trafficking can result in sustained activation of Ras at the Golgi.

Narat J Eungdamrong, Ravi Iyengar

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Basal State Calibration of a Chemical Reaction Network Model for Autophagy.International journal of molecular sciences · 2024
    Article
  4. Article
  5. Systems biology of cellular membranes: a convergence with biophysics.Wiley interdisciplinary reviews. Systems biology and medicine · 2017
    Review
  6. PLCε signaling in cancer.Journal of cancer research and clinical oncology · 2016
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Use of virtual cell in studies of cellular dynamics.International review of cell and molecular biology · 2010
    Review
  13. Topology-based abstraction of complex biological systems: application to the Golgi apparatus.Theory in biosciences = Theorie in den Biowissenschaften · 2008
    Review
  14. Modelling cellular signalling systems.Essays in biochemistry · 2008
    Review
  15. Article
  16. Modeling of spatially-restricted intracellular signaling.Wiley interdisciplinary reviews. Systems biology and medicine
    Review
  17. Models at the single cell level.Wiley interdisciplinary reviews. Systems biology and medicine
    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

2 authors at 1 institution in 1 country.

Narat J EungdamrongDepartment of Pharmacology and Biological Chemistry, Mount Sinai School of Medicine, New York, New York 10029, USA.
Ravi Iyengar
Icahn School of Medicine at Mount Sinai · US

Funding

MOLECULAR MECHANISM OF DESENSITIZATIONR01GM054508 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI IYENGAR, SRINIVAS RAVI V · 1995 to 2016
$8.0M
NIGMS NIH HHS GM 54508NIGMS NIH HHS GM 73853NIGMS NIH HHS R01 GM054508
6 · The paper itself

Abstract

Imaging experiments have shown that cell signaling components such as Ras can be activated by growth factors at distinct subcellular locations. Trafficking between these subcellular locations is a regulated dynamic process. The effects of trafficking and the molecular mechanisms underlying compartment-specific Ras activation were studied using numerical simulations of an ordinary differential equation-based multi-compartment model. The simulations show that interplay between two distinct mechanisms, a palmitoylation cycle that controls Ras trafficking and a phospholipase C-epsilon (PLC-epsilon) driven feedback loop, can convert a transient calcium signal into prolonged Ras activation at the Golgi. Detailed analysis of the network identified PLC-epsilon as a key determinant of "compartment switching". Modulation of PLC-epsilon activity switches the location of activated Ras between the plasma membrane and Golgi through a new mechanism termed "kinetic scaffolding". These simulations indicate that multiple biochemical mechanisms, when appropriately coupled, can give rise to an intracellular compartment-specific sustained Ras activation in response to stimulation of growth factor receptors at the plasma membrane.

Indexed as

Models, BiologicalCalcium SignalingCell MembraneComputer SimulationFeedbackGolgi ApparatusPhosphoinositide Phospholipase CProtein Transportras ProteinsReceptors, Growth FactorSignal TransductionType C PhospholipasesPhosphoinositide Phospholipase Cphospholipase C epsilonras ProteinsReceptors, Growth FactorType C Phospholipases

Identifiers

PMID17098795
PMCPMC1779960
OpenAlexW1999982244

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.