Evidence map›Paper›PMID 39459333›Full record

ArticleMolecules (Basel, Switzerland)2024

Protein A-like Peptide Design Based on Diffusion and ESM2 Models.

Long Zhao, Qiang He, Huijia Song, Tianqian Zhou, An Luo, Zhenguo Wen, Teng Wang, Xiaozhu Lin

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Protein A-like peptide generation based on generalized diffusion model.Journal of computer-aided molecular design · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. 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

8 authors.

Long ZhaoDepartment of Pharmaceutics, Beijing Institute of Petrochemical Technology, Beijing 102627, China.ORCID 0009-0006-1229-2583
Qiang HeDepartment of Pharmaceutics, Beijing Institute of Petrochemical Technology, Beijing 102627, China.
Huijia SongDepartment of Computer Science, Beijing Institute of Petrochemical Technology, Beijing 102627, China.ORCID 0009-0004-9121-4318
Tianqian ZhouDepartment of Computer Science, Beijing Institute of Petrochemical Technology, Beijing 102627, China.ORCID 0009-0005-5517-4483
An LuoDepartment of Pharmaceutics, Beijing Institute of Petrochemical Technology, Beijing 102627, China.
Zhenguo WenDepartment of Pharmaceutics, Beijing Institute of Petrochemical Technology, Beijing 102627, China.ORCID 0009-0006-4375-8462
Teng WangDepartment of Pharmaceutics, Beijing Institute of Petrochemical Technology, Beijing 102627, China.
Xiaozhu LinDepartment of Computer Science, Beijing Institute of Petrochemical Technology, Beijing 102627, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteins are the foundation of life, and designing functional proteins remains a key challenge in biotechnology. Before the development of AlphaFold2, the focus of design was primarily on structure-centric approaches such as using the well-known open-source software Rosetta3. Following the development of AlphaFold2, deep-learning techniques for protein design gained prominence. This study proposes a new method to generate functional proteins using the diffusion model and ESM2 protein language model. Diffusion models, which are widely used in image and natural language generation, are used here for protein design, facilitating the controlled generation of new sequences. The ESM2 model, trained on the basis of large-scale protein sequence data, provides a deep understanding of the context of the sequence, thus improving the model's ability to generate biologically relevant proteins. In this study, we used the Protein A-like peptide as a model study object, combined the diffusion model and the ESM2 model to generate new peptide sequences from minimal input data, and verified their biological activities through experiments such as the BLI affinity test. In conclusion, we developed a new method for protein design that provides a novel strategy to meet the challenges of generic protein generation.

Indexed as

PeptidesAmino Acid SequenceDiffusionModels, MolecularProtein EngineeringSoftwarePeptidesbiological activitydiffusion modelESM2peptide screeningprotein design

Identifiers

PMID39459333
PMCPMC11510650

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.