Evidence map›Paper›PMID 37663788›Full record

ArticleFrontiers in bioinformatics2023

Improved prediction of MHC-peptide binding using protein language models.

Nasser Hashemi, Boran Hao, Mikhail Ignatov, Ioannis Ch Paschalidis, Pirooz Vakili, Sandor Vajda, Dima Kozakov

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
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

7 authors at 2 institutions in 1 country.

Nasser HashemiDivision of Systems Engineering, Boston University, Boston, MA, United States.
Boran HaoDepartment of Electrical and Computer Engineering, Boston University, Boston, MA, United States.
Mikhail IgnatovDepartment of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY, United States.
Ioannis Ch PaschalidisDivision of Systems Engineering, Boston University, Boston, MA, United States.
Pirooz VakiliDivision of Systems Engineering, Boston University, Boston, MA, United States.
Sandor VajdaDivision of Systems Engineering, Boston University, Boston, MA, United States.
Dima KozakovDepartment of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY, United States.
Boston University · USStony Brook University · US

Funding

Analysis and Prediction of Molecular InteractionsR35GM118078 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SANDOR VAJDA · 2016 to 2026
$6.5M
Simulation of Multi-Protein systemsR01GM140098 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI KOZAKOV, DMYTRO · 2021 to 2024
$1.4M
Optimizing and Learning Strategies for Protein Docking R01GM135930 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI VAKILI, PIROOZ · 2019 to 2021
$561k
NIGMS NIH HHS R01 GM135930NIGMS NIH HHS R01 GM140098NIGMS NIH HHS R35 GM118078
6 · The paper itself

Abstract

Major histocompatibility complex Class I (MHC-I) molecules bind to peptides derived from intracellular antigens and present them on the surface of cells, allowing the immune system (T cells) to detect them. Elucidating the process of this presentation is essential for regulation and potential manipulation of the cellular immune system. Predicting whether a given peptide binds to an MHC molecule is an important step in the above process and has motivated the introduction of many computational approaches to address this problem. NetMHCPan, a pan-specific model for predicting binding of peptides to any MHC molecule, is one of the most widely used methods which focuses on solving this binary classification problem using shallow neural networks. The recent successful results of Deep Learning (DL) methods, especially Natural Language Processing (NLP-based) pretrained models in various applications, including protein structure determination, motivated us to explore their use in this problem. Specifically, we consider the application of deep learning models pretrained on large datasets of protein sequences to predict MHC Class I-peptide binding. Using the standard performance metrics in this area, and the same training and test sets, we show that our models outperform NetMHCpan4.1, currently considered as the-state-of-the-art.

Indexed as

cellular immune systemdeep learningMHC class Inatural language processingtransformers

Identifiers

PMID37663788
PMCPMC10469926
OpenAlexW4385982832

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.