Evidence map›Paper›PMID 27508440›Full record

ArticleBiophysical journal2016

Association of Endophilin B1 with Cytoplasmic Vesicles.

Jinhui Li, Barbara Barylko, John P Eichorst, Joachim D Mueller, Joseph P Albanesi, Yan Chen

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  5. Screening and identification of protein 29 ofFrontiers in cellular and infection microbiology · 2025
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  7. Review
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  9. Article
  10. MuRF1/TRIM63, Master Regulator of Muscle Mass.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Article
  13. 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

6 authors at 2 institutions in 1 country.

Jinhui LiDepartment of Physics, University of Minnesota, Minneapolis, Minnesota.
Barbara BarylkoUT Southwestern Medical Center, Dallas, Texas.
John P EichorstDepartment of Physics, University of Minnesota, Minneapolis, Minnesota.
Joachim D MuellerSchool of Physics and Astronomy, University of Minnesota, Minneapolis, Minnesota.
Joseph P AlbanesiUT Southwestern Medical Center, Dallas, Texas.
Yan ChenDepartment of Physics, University of Minnesota, Minneapolis, Minnesota. Electronic address: chen@physics.umn.edu.
University of Minnesota · USSouthwestern Medical Center · US

Funding

TRAINING-PULMONARY CELL &MOLECULAR BIOLOGY &PHYSIOLOGYT32HL007741 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI DUDLEY, R. ADAMS, INGBAR, DAVID H · 1994 to 2023
$13.9M
Structural Characterization of APOBECS's Atomic interactionsP01GM091743 · NIGMS · UNIVERSITY OF MINNESOTA · PI KOTLER, MOSHE · 2011 to 2015
$10.1M
In vivo Fluorescence Fluctuation Spectroscopy - Administrative SupplementR01GM064589 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MUELLER, JOACHIM D · 2002 to 2019
$4.6M
NHLBI NIH HHS T32 HL007741NIGMS NIH HHS P01 GM091743NIGMS NIH HHS R01 GM064589
6 · The paper itself

Abstract

Endophilins are SH3- and BAR domain-containing proteins implicated in membrane remodeling and vesicle formation. Endophilins A1 and A2 promote the budding of endocytic vesicles from the plasma membrane, whereas endophilin B1 has been implicated in vesicle budding from intracellular organelles, including the trans-Golgi network and late endosomes. We previously reported that endophilins A1 and A2 exist almost exclusively as soluble dimers in the cytosol. Here, we present results of fluorescence fluctuation spectroscopy analyses indicating that, in contrast, the majority of endophilin B1 is present in multiple copies on small, highly mobile cytoplasmic vesicles. Formation of these vesicles was enhanced by overexpression of wild-type dynamin 2, but suppressed by expression of a catalytically inactive dynamin 2 mutant. Using dual-color heterospecies partition analysis, we identified the epidermal growth factor receptor on endophilin B1 vesicles. Moreover, a proportion of endophilin B1 vesicles also contained caveolin, whereas clathrin was almost undetectable on those vesicles. These results raise the possibility that endophilin B1 participates in dynamin 2-dependent formation of a population of transport vesicles distinct from those generated by A-type endophilins.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCaveolinsCell LineCytoplasmic VesiclesDynamin IIIErbB ReceptorsHumansLigandsProtein BindingProtein TransportRatsAdaptor Proteins, Signal TransducingCaveolinsDynamin IIIEGFR protein, humanErbB ReceptorsLigandsSH3GLB1 protein, human

Identifiers

PMID27508440
PMCPMC4982929
OpenAlexW2492175253

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.