Evidence map›Paper›PMID 37399105›Full record

ArticleBioinformatics (Oxford, England)2023

Generating interacting protein sequences using domain-to-domain translation.

Barthelemy Meynard-Piganeau, Caterina Fabbri, Martin Weigt, Andrea Pagnani, Christoph Feinauer

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Pairing interacting protein sequences using masked language modeling.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Barthelemy Meynard-PiganeauComputational and Quantitative Biology, LCQB UMR 7238, Institut de Biologie Paris Seine, CNRS, Sorbonne Université, Paris 75005, France.
Caterina FabbriDepartment of Computing Sciences, Bocconi University, Milan 20100, Italy.
Martin WeigtComputational and Quantitative Biology, LCQB UMR 7238, Institut de Biologie Paris Seine, CNRS, Sorbonne Université, Paris 75005, France.ORCID 0000-0002-0492-3684
Andrea PagnaniPolitecnico di Torino, Duca degli Abruzzi, 24, Turin 10129, Italy.ORCID 0000-0002-6509-0807
Christoph FeinauerDepartment of Computing Sciences, Bocconi University, Milan 20100, Italy.ORCID 0000-0002-8941-7333

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationBeing able to artificially design novel proteins of desired function is pivotal in many biological and biomedical applications. Generative statistical modeling has recently emerged as a new paradigm for designing amino acid sequences, including in particular models and embedding methods borrowed from natural language processing (NLP). However, most approaches target single proteins or protein domains, and do not take into account any functional specificity or interaction with the context. To extend beyond current computational strategies, we develop a method for generating protein domain sequences intended to interact with another protein domain. Using data from natural multidomain proteins, we cast the problem as a translation problem from a given interactor domain to the new domain to be generated, i.e. we generate artificial partner sequences conditional on an input sequence. We also show in an example that the same procedure can be applied to interactions between distinct proteins.

resultsEvaluating our model's quality using diverse metrics, in part related to distinct biological questions, we show that our method outperforms state-of-the-art shallow autoregressive strategies. We also explore the possibility of fine-tuning pretrained large language models for the same task and of using Alphafold 2 for assessing the quality of sampled sequences. AVAILABILITY AND IMPLEMENTATION: Data and code on https://github.com/barthelemymp/Domain2DomainProteinTranslation.

Indexed as

LanguageProteinsAmino Acid SequenceProtein DomainsProteins

Identifiers

PMID37399105
PMCPMC10329493

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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.