Evidence map›Paper›PMID 36460640›Full record

ArticleNature communications2022

Discrete LAT condensates encode antigen information from single pMHC:TCR binding events.

Darren B McAffee, Mark K O'Dair, Jenny J Lin, Shalini T Low-Nam, Kiera B Wilhelm, Sungi Kim, Shumpei Morita, Jay T Groves

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.2field-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

42 citing papers in PubMed, 57 citations in OpenAlex.

  1. LAT condensation gates PLCγ1 activation via bimodal LAT phosphorylation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Decondensing cancer immunotherapy.Science (New York, N.Y.) · 2026
    Article
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  15. A unifying model of LAT condensates in reconstitution experiments.bioRxiv : the preprint server for biology · 2025
    Article
  16. Article
  17. Parallel reactions on a single T cell receptor offer a robust kinetic proofreading mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  18. Review
  19. Review
  20. Interfacial effects determine nonequilibrium phase behaviors in chemically driven fluids.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

8 authors at 2 institutions in 2 countries.

Darren B McAffeeDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.ORCID 0000-0002-2565-4938
Mark K O'DairDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.ORCID 0000-0002-8113-2229
Jenny J LinDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.
Shalini T Low-NamDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.
Kiera B WilhelmDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.ORCID 0000-0002-8781-7739
Sungi KimDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.
Shumpei MoritaDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA.
Jay T GrovesDepartment of Chemistry, University of California, Berkeley, Berkeley, CA, 94720, USA. jtgroves@lbl.gov.ORCID 0000-0002-3037-5220
University of California, Berkeley · USNanyang Technological University · SG

Funding

Understand the metabolic fitness of naïve T cellsP01AI091580 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JEROEN ROOSE · 2011 to 2026
$31.1M
NIAID NIH HHS P01 AI091580
6 · The paper itself

Abstract

LAT assembly into a two-dimensional protein condensate is a prominent feature of antigen discrimination by T cells. Here, we use single-molecule imaging techniques to resolve the spatial position and temporal duration of each pMHC:TCR molecular binding event while simultaneously monitoring LAT condensation at the membrane. An individual binding event is sufficient to trigger a LAT condensate, which is self-limiting, and neither its size nor lifetime is correlated with the duration of the originating pMHC:TCR binding event. Only the probability of the LAT condensate forming is related to the pMHC:TCR binding dwell time. LAT condenses abruptly, but after an extended delay from the originating binding event. A LAT mutation that facilitates phosphorylation at the PLC-γ1 recruitment site shortens the delay time to LAT condensation and alters T cell antigen specificity. These results identify a function for the LAT protein condensation phase transition in setting antigen discrimination thresholds in T cells.

Indexed as

Diffusion Magnetic Resonance ImagingReceptors, Antigen, T-CellLymphocyte CountPhosphorylationT-Cell Antigen Receptor SpecificityReceptors, Antigen, T-Cell

Identifiers

PMID36460640
PMCPMC9718779
OpenAlexW4311121641

What OpenQuestion holds

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Registered trials

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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.