Evidence map›Paper›PMID 28255696›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2017

Reconstitution of TCR Signaling Using Supported Lipid Bilayers.

Xiaolei Su, Jonathon A Ditlev, Michael K Rosen, Ronald D Vale

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Protein interactions, calcium, phosphorylation, and cholesterol modulate CFTR cluster formation on membranes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. The physical landscape of CAR-T synapse.Biophysical journal · 2024
    Review
  8. Article
  9. Review
  10. Leveraging DNA Origami to Study Phagocytosis.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  11. Biomolecular Condensation of SH2 Domain-Containing Proteins on Membranes.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  12. Article
  13. Article
  14. Phase separation in immune signalling.Nature reviews. Immunology · 2022
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Retromer forms low order oligomers on supported lipid bilayers.The Journal of biological chemistry · 2020
    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

4 authors at 4 institutions in 1 country.

Xiaolei SuMarine Biological Laboratory, The HHMI Summer Institute, Woods Hole, MA, 02543, USA.
Jonathon A DitlevMarine Biological Laboratory, The HHMI Summer Institute, Woods Hole, MA, 02543, USA.
Michael K RosenMarine Biological Laboratory, The HHMI Summer Institute, Woods Hole, MA, 02543, USA.
Ronald D ValeMarine Biological Laboratory, The HHMI Summer Institute, Woods Hole, MA, 02543, USA. ron.vale@ucsf.edu.
Howard Hughes Medical Institute · USMarine Biological Laboratory · USSouthwestern Medical Center · USUniversity of California, San Francisco · US

Funding

STRUCTURAL STUDY OF RHO-GTPASE REGULATORS AND EFFECTORSR01GM056322 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ROSEN, MICHAEL K · 1997 to 2019
$5.7M
Stability and dynamics of nephrin/Nck/N-WASp clusters on membranesF32DK101188 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI DITLEV, JONATHON A · 2014 to 2016
$164k
Howard Hughes Medical InstituteNIDDK NIH HHS F32 DK101188NIGMS NIH HHS R01 GM056322
6 · The paper itself

Abstract

Biochemical reconstitution has served as an important tool for understanding the mechanisms of many cellular processes including DNA replication, transcription, translation, vesicle trafficking, and ubiquitin-mediated proteolysis. Here, we demonstrate that biochemical reconstitution can be applied to studying a complex signaling pathway involving as many as 12 proteins or protein complexes acting at the surface of model membranes. We show that a temporal sequence of events in activated T cells beginning with phosphorylation of the T cell receptor and culminating in the activation of actin polymerization can be replicated in vitro. Our reconstitution demonstrates the sufficiency of these proteins in producing many of the complex behaviors observed during T cell activation. The ability to manipulate all of the components, measure reaction rates, and observe molecular behaviors, including at single molecule resolution, has enabled us to gain insight into some of the important biochemical features of this signaling pathway such as microcluster formation. The same system could be adapted to study other membrane-proximal signaling pathways, including growth factor receptors, death receptors, and Eph receptors.

Indexed as

Lymphocyte ActivationSignal TransductionAnimalsCell-Free SystemHumansLipid BilayersReceptors, Antigen, T-CellT-LymphocytesLipid BilayersReceptors, Antigen, T-CellActinLATMicroclusterMultivalencyPhase separationReconstitutionSupported lipid bilayerTCR

Identifiers

PMID28255696
PMCPMC5633369
OpenAlexW2592563316

What OpenQuestion holds

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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.