Evidence map›Paper›PMID 37140040›Full record

ArticleNucleic acids research2023

TCRmodel2: high-resolution modeling of T cell receptor recognition using deep learning.

Rui Yin, Helder V Ribeiro-Filho, Valerie Lin, Ragul Gowthaman, Melyssa Cheung, Brian G Pierce

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
14.3field-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

83 citing papers in PubMed, 93 citations in OpenAlex.

  1. A p53Molecular therapy. Oncology · 2026
    Article
  2. Review
  3. Structural basis for T-cell receptor recognition of p53Acta crystallographica. Section D, Structural biology · 2026
    Article
  4. T Cell Thoughts.Immunological reviews · 2026
    Review
  5. Article
  6. Article
  7. Ensembles ofbioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
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  15. Article
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23 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 2 institutions in 2 countries.

Rui YinUniversity of Maryland Institute for Bioscience and Biotechnology Research, Rockville, MD 20850, USA.
Helder V Ribeiro-FilhoUniversity of Maryland Institute for Bioscience and Biotechnology Research, Rockville, MD 20850, USA.
Valerie LinUniversity of Maryland Institute for Bioscience and Biotechnology Research, Rockville, MD 20850, USA.
Ragul GowthamanUniversity of Maryland Institute for Bioscience and Biotechnology Research, Rockville, MD 20850, USA.
Melyssa CheungUniversity of Maryland Institute for Bioscience and Biotechnology Research, Rockville, MD 20850, USA.
Brian G PierceUniversity of Maryland Institute for Bioscience and Biotechnology Research, Rockville, MD 20850, USA.ORCID 0000-0003-4821-0368
Advanced Bioscience Laboratories (United States) · USUniversity of Maryland, Baltimore · US

Funding

High resolution modeling and design of immune recognitionR35GM144083 · NIGMS · UNIV OF MARYLAND, COLLEGE PARK · PI Brian G. Pierce · 2022 to 2026
$1.6M
NIGMS NIH HHS R35 GM144083
6 · The paper itself

Abstract

The cellular immune system, which is a critical component of human immunity, uses T cell receptors (TCRs) to recognize antigenic proteins in the form of peptides presented by major histocompatibility complex (MHC) proteins. Accurate definition of the structural basis of TCRs and their engagement of peptide-MHCs can provide major insights into normal and aberrant immunity, and can help guide the design of vaccines and immunotherapeutics. Given the limited amount of experimentally determined TCR-peptide-MHC structures and the vast amount of TCRs within each individual as well as antigenic targets, accurate computational modeling approaches are needed. Here, we report a major update to our web server, TCRmodel, which was originally developed to model unbound TCRs from sequence, to now model TCR-peptide-MHC complexes from sequence, utilizing several adaptations of AlphaFold. This method, named TCRmodel2, allows users to submit sequences through an easy-to-use interface and shows similar or greater accuracy than AlphaFold and other methods to model TCR-peptide-MHC complexes based on benchmarking. It can generate models of complexes in 15 minutes, and output models are provided with confidence scores and an integrated molecular viewer. TCRmodel2 is available at https://tcrmodel.ibbr.umd.edu.

Indexed as

Deep LearningAntigensComputer SimulationHumansPeptidesReceptors, Antigen, T-CellAntigensPeptidesReceptors, Antigen, T-Cell

Identifiers

PMID37140040
PMCPMC10320165
OpenAlexW4368357399

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.