Evidence map›Paper›PMID 27697928›Full record

ArticleThe Journal of cell biology2016

Nanoscopic compartmentalization of membrane protein motion at the axon initial segment.

David Albrecht, Christian M Winterflood, Mohsen Sadeghi, Thomas Tschager, Frank Noé, Helge Ewers

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 119 citations in OpenAlex.

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5 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 3 countries.

David AlbrechtInstitute for Chemistry and Biochemistry, Free University Berlin, 14195 Berlin, Germany Randall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, England, UK Institute for Biochemistry, ETH Zurich, 8093 Zurich, Switzerland.ORCID http://orcid.org/0000-0001-9455-1134
Christian M WinterfloodRandall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, England, UK Institute for Biochemistry, ETH Zurich, 8093 Zurich, Switzerland.ORCID http://orcid.org/0000-0001-5621-3695
Mohsen SadeghiDepartment of Mathematics and Computer Science, Free University Berlin, 14195 Berlin, Germany.ORCID http://orcid.org/0000-0002-7698-5630
Thomas TschagerInstitute for Biochemistry, ETH Zurich, 8093 Zurich, Switzerland.ORCID http://orcid.org/0000-0003-3323-034X
Frank NoéDepartment of Mathematics and Computer Science, Free University Berlin, 14195 Berlin, Germany.ORCID http://orcid.org/0000-0003-4169-9324
Helge EwersInstitute for Chemistry and Biochemistry, Free University Berlin, 14195 Berlin, Germany Randall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, England, UK Institute for Biochemistry, ETH Zurich, 8093 Zurich, Switzerland helge.ewers@fu-berlin.de.ORCID http://orcid.org/0000-0003-3948-4332
King's College London · GBFreie Universität Berlin · DEETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The axon initial segment (AIS) is enriched in specific adaptor, cytoskeletal, and transmembrane molecules. During AIS establishment, a membrane diffusion barrier is formed between the axonal and somatodendritic domains. Recently, an axonal periodic pattern of actin, spectrin, and ankyrin forming 190-nm-spaced, ring-like structures has been discovered. However, whether this structure is related to the diffusion barrier function is unclear. Here, we performed single-particle tracking time-course experiments on hippocampal neurons during AIS development. We analyzed the mobility of lipid-anchored molecules by high-speed single-particle tracking and correlated positions of membrane molecules with the nanoscopic organization of the AIS cytoskeleton. We observe a strong reduction in mobility early in AIS development. Membrane protein motion in the AIS plasma membrane is confined to a repetitive pattern of ∼190-nm-spaced segments along the AIS axis as early as day in vitro 4, and this pattern alternates with actin rings. Mathematical modeling shows that diffusion barriers between the segments significantly reduce lateral diffusion along the axon.

Indexed as

Cell CompartmentationAnimalsAxon Initial SegmentCells, CulturedCell TrackingDiffusionGlycosylphosphatidylinositolsGreen Fluorescent ProteinsHippocampusMembrane ProteinsNanoparticlesNeuronsQuantum DotsRats, Sprague-DawleySpectrinGlycosylphosphatidylinositolsGreen Fluorescent ProteinsMembrane ProteinsSpectrin

Identifiers

PMID27697928
PMCPMC5057285
OpenAlexW2952892759

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.