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Updated: Jul 15, 2026

Construction of Cyclic Cell-Penetrating Peptides for Enhanced Penetration of Biological Barriers
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Published on: September 19, 2022

CPP2Vec: A representation learning approach for cell-penetrating peptides prediction.

Stavroula Svolou1, Vasileios Konstantakos2,3,4, Anastasia Krithara1

  • 1Institute of Informatics and Telecommunications, NCSR "Demokritos", Agia Paraskevi, Greece.

Plos Computational Biology
|July 13, 2026
PubMed
Summary

This study introduces CPP2Vec, a novel machine learning tool that uses Word2Vec to predict cell-penetrating peptides (CPPs) for enhanced drug delivery. CPP2Vec offers efficient and accurate identification of therapeutic peptides, aiding in Duchenne Muscular Dystrophy treatment research.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Drug Delivery

Background:

  • Cell-penetrating peptides (CPPs) are crucial for delivering therapeutic molecules, including antisense oligonucleotides (ASOs), across cell membranes.
  • Peptide nucleic acids (PNAs) and phosphorodiamidate morpholino oligomers (PMOs) are key ASOs investigated for Duchenne Muscular Dystrophy (DMD).
  • In silico methods are increasingly used to discover novel CPPs, offering a cost-effective alternative to experimental approaches.

Purpose of the Study:

  • To develop CPP2Vec, a Word2Vec-based machine learning method for predicting CPPs and their delivery efficiency.
  • To create a hybrid dataset (CPP2Vec-GenSet) integrating computational and experimental data to improve CPP representation learning.
  • To build and evaluate task-specific models for CPP classification, uptake efficiency prediction, and PMO delivery enhancement.

Main Methods:

  • Utilized the Word2Vec technique to learn representations from amino acid sequences of peptides.
  • Constructed CPP2Vec-GenSet, a hybrid dataset combining computationally generated and experimentally validated CPPs.
  • Developed supervised machine learning models for CPP-Classification, Uptake-Efficiency, and PMO-Delivery, and explored Large Language Models (LLMs) like ProtT5, ProtBERT, and ESM-2 for embeddings.

Main Results:

  • CPP2Vec demonstrated robust predictive performance and generalization across classification, efficiency, and delivery tasks.
  • The method achieved high computational efficiency compared to existing state-of-the-art CPP prediction tools.
  • Alternative models using LLM embeddings (CPP2LLM) were also explored, showing competitive results.

Conclusions:

  • CPP2Vec provides a reproducible and efficient in silico tool for identifying and prioritizing CPPs with therapeutic potential.
  • The Word2Vec approach effectively learns peptide representations directly from sequence data.
  • This ML-based tool supports early-stage research for CPPs relevant to diseases like DMD.