Evidence map›Paper›PMID 41795657›Full record

ArticleBriefings in bioinformatics2026

De novo functional protein sequence generation: overcoming data scarcity through regeneration and large language models.

Chenyu Ren, Daihai He, Jian Huang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Chenyu RenDepartment of Applied Mathematics, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.
Daihai HeDepartment of Applied Mathematics, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.ORCID 0000-0003-3253-654X
Jian HuangDepartment of Applied Mathematics, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.ORCID 0000-0002-5218-9269

Funding

Hong Kong Polytechnic UniversityResearch Centre for the Mathematical Foundations of Generative AI P0046811
6 · The paper itself

Abstract

Proteins are essential components of all living organisms and play a critical role in cellular survival. They have a broad range of applications, from clinical treatments to material engineering. This versatility has spurred the development of protein design, with amino acid sequence design being a crucial step in the process. Recent advancements in deep generative models have shown promise for protein sequence design. However, the scarcity of functional protein sequence data for certain types can hinder the training of these models, which often require large datasets. To address this challenge, we propose a hierarchical model named ProteinRG that can generate functional protein sequences using relatively small datasets. ProteinRG begins by generating a representation of a protein sequence, leveraging existing large protein sequence models, before producing a functional protein sequence. We have tested our model on various functional protein sequences and evaluated the results from three perspectives: multiple sequence alignment, t-SNE distribution analysis, and 3D structure prediction. The findings indicate that our generated protein sequences maintain both similarity to the original sequences and consistency with the desired functions. Moreover, our model demonstrates superior performance compared twith other generative models for protein sequence generation.

Indexed as

Computational BiologyProteinsSequence Analysis, ProteinAmino Acid SequenceDatabases, ProteinGenerative Artificial IntelligenceLarge Language ModelsModels, MolecularProtein ConformationSequence AlignmentProteinsgenerative modelslarge language modelsprotein designrepresentation learningsmall sample size

Identifiers

PMID41795657
PMCPMC12967336

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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.