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Author Spotlight: A Computational Approach to Decipher Amino Acid Preferences in Multispecific Protein-Protein Interactions
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pLM4ACE: A protein language model based predictor for antihypertensive peptide screening.

Zhenjiao Du1, Xingjian Ding2, William Hsu2

  • 1Department of Grain Science and Industry, Kansas State University, Manhattan, KS 66506, USA.

Food Chemistry
|August 21, 2023
PubMed
Summary

This study developed a protein language model using evolutionary scale modeling (ESM-2) embeddings to identify peptides that inhibit angiotensin-I converting enzyme (ACE). The ESM-2 approach significantly improved prediction accuracy for ACE inhibitors.

Keywords:
ACE inhibitory peptideAntihypertensionBioactive peptideMachine learningProtein language model

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Area of Science:

  • Biotechnology
  • Computational Biology
  • Pharmacology

Background:

  • Angiotensin-I converting enzyme (ACE) is a key regulator of the renin-angiotensin system.
  • ACE is a validated drug target for managing hypertension.
  • Developing effective ACE inhibitors is crucial for cardiovascular health.

Purpose of the Study:

  • To develop and validate a protein language model (pLM) for screening ACE inhibitory peptides.
  • To leverage evolutionary scale modeling (ESM-2) embeddings for enhanced peptide activity prediction.
  • To compare the performance of ESM-2 embeddings against traditional peptide embedding methods.

Main Methods:

  • Utilized ESM-2 embeddings for a protein language model.
  • Trained and evaluated 65 different classifiers on experimental data.
  • Compared ESM-2 with 12 conventional peptide embedding techniques and 5 machine learning models.
  • Assessed model performance using balanced accuracy (BACC), Matthews correlation coefficient (MCC), and area under the curve (AUC).

Main Results:

  • Logistic regression combined with ESM-2 embeddings achieved the highest performance (BACC: 0.883 ± 0.017, MCC: 0.77 ± 0.032, AUC: 0.96 ± 0.009).
  • ESM-2 embeddings demonstrated superior performance over 12 traditional embedding methods.
  • Multilayer perceptron and support vector machine models also showed strong compatibility with ESM-2 embeddings.

Conclusions:

  • ESM-2 embeddings provide a powerful tool for enhancing the prediction of ACE inhibitory peptide activity.
  • The developed models offer a promising approach for discovering novel ACE inhibitors.
  • A publicly accessible webserver is available for utilizing the top-performing models.