Evidence map›Paper›PMID 28340336›Full record

ArticleCell2017

A DNA-Based T Cell Receptor Reveals a Role for Receptor Clustering in Ligand Discrimination.

Marcus J Taylor, Kabir Husain, Zev J Gartner, Satyajit Mayor, Ronald D Vale

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

85 citing papers in PubMed, 202 citations in OpenAlex.

  1. Inhibitory Fc Receptor sets a time limit on macrophage response to IgG.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Solution structure and synaptic analyses reveal determinants of bispecific T cell engager potency.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Physical extraction of antigen and information.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Differential roles of kinetic on- and off-rates in T-cell receptor signal integration revealed with a modified Fab'-DNA ligand.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Development of a highly sensitive platform for protein-protein interaction detection and regulation of T cell function.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Review
  15. Mechanical force determines chimeric antigen receptor microclustering and signaling.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Challenges of Protein-Protein Docking of the Membrane Proteins.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  20. Article

25 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

5 authors at 4 institutions in 2 countries.

Marcus J TaylorDepartment of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94143, USA; National Centre for Biological Sciences, Bangalore 560065, India; HHMI Summer Institute, Woods Hole, MA 02543, USA.
Kabir HusainNational Centre for Biological Sciences, Bangalore 560065, India; The Simons Centre for the Study of Living Machines, Bangalore 560065, India.
Zev J GartnerDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA 94143, USA.
Satyajit MayorNational Centre for Biological Sciences, Bangalore 560065, India; HHMI Summer Institute, Woods Hole, MA 02543, USA. Electronic address: mayor@ncbs.res.in.
Ronald D ValeDepartment of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94143, USA; Howard Hughes Medical Institute, University of California San Francisco, San Francisco, CA 94143, USA; HHMI Summer Institute, Woods Hole, MA 02543, USA. Electronic address: ron.vale@ucsf.edu.
National Centre for Biological Sciences · INHoward Hughes Medical Institute · USUniversity of California, San Francisco · USWoodwell Climate Research Center · US

Funding

DBT-Wellcome Trust India Alliance IA/M/15/1/502018Howard Hughes Medical InstituteWellcome TrustWellcome Trust IA/M/15/1/502018
6 · The paper itself

Abstract

A T cell mounts an immune response by measuring the binding strength of its T cell receptor (TCR) for peptide-loaded MHCs (pMHC) on an antigen-presenting cell. How T cells convert the lifetime of the extracellular TCR-pMHC interaction into an intracellular signal remains unknown. Here, we developed a synthetic signaling system in which the extracellular domains of the TCR and pMHC were replaced with short hybridizing strands of DNA. Remarkably, T cells can discriminate between DNA ligands differing by a single base pair. Single-molecule imaging reveals that signaling is initiated when single ligand-bound receptors are converted into clusters, a time-dependent process requiring ligands with longer bound times. A computation model reveals that receptor clustering serves a kinetic proofreading function, enabling ligands with longer bound times to have disproportionally greater signaling outputs. These results suggest that spatial reorganization of receptors plays an important role in ligand discrimination in T cell signaling.

Indexed as

LigandsSignal TransductionDNAHumansJurkat CellsPhosphorylationReceptors, Antigen, T-CellSingle Molecule ImagingT-LymphocytesZAP-70 Protein-Tyrosine KinaseDNALigandsReceptors, Antigen, T-CellZAP70 protein, humanZAP-70 Protein-Tyrosine Kinase

Identifiers

PMID28340336
PMCPMC6934412
OpenAlexW2602990311

What OpenQuestion holds

Textmetadata
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.