Evidence map›Paper›PMID 42608825›Full record

ArticleBioinformatics (Oxford, England)2026

Bridging linguistic reasoning and biophysical reality toward peptide engineering via instruction-tuned language modeling.

Kaijun Yang, Tianxiang Wu, Wenbo Zhang, Pengyong Li

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kaijun YangSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.
Tianxiang WuSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.
Wenbo ZhangSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.
Pengyong LiSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.ORCID 0000-0001-5971-046X

Funding

National Natural Science Foundation of China 62572374National Natural Science Foundation of China U22A2037
6 · The paper itself

Abstract

motivationPeptides serve as critical mediators in biological systems, regulating essential processes ranging from neurotransmission to immune response. However, their nonlinear sequence-function relationships and immense chemical diversity pose significant challenges for efficient experimental characterization and therapeutic development. While Protein Language Models have advanced biological sequence understanding, they predominantly capture global evolutionary features of full-length proteins, often overlooking the local physicochemical dependencies and short-range residue interactions that are essential for defining peptide bioactivity.

resultsTo address this gap, we leverage the linguistic competence of general-purpose Large Language Models (LLMs) to treat amino acid sequences as "biological text," bridging natural language supervision with biochemical sequence modeling without relying on explicit structural or evolutionary priors. We curate a peptide-specific instruction dataset, Pep-Instructions, spanning function description, sequence design, property prediction, and physicochemical optimization, and adapt a general-purpose LLM through parameter-efficient instruction tuning. Extensive benchmarking against general-purpose language models shows consistent improvements across the evaluated peptide-centric tasks. In particular, the instruction-tuned model produces more semantically faithful functional descriptions, generates peptide sequences with stronger sequence-level similarity, with representative ESMFold case studies suggesting backbone-level consistency, improves prediction of diverse peptide properties, and enables more reliable directional optimization of physicochemical properties under the adopted in silico evaluation protocols. Overall, these results establish Pep-Instructions as a unified benchmark and demonstrate the value of peptide-specific instruction tuning for peptide understanding, prediction, and design. AVAILABILITY AND IMPLEMENTATION: Source code and Pep-Instructions are available at https://github.com/kjY7836/pepinstruction. Fine-tuned model weights are available at https://huggingface.co/Codelife176/Pep-instruction.

Indexed as

LinguisticsPeptidesProtein EngineeringAmino Acid SequenceLarge Language ModelsPeptides

Identifiers

PMID42608825
PMCPMC13529362

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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.