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Related Experiment Video

Updated: Feb 5, 2026

Construction of Cyclic Cell-Penetrating Peptides for Enhanced Penetration of Biological Barriers
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CPPred-FL: a sequence-based predictor for large-scale identification of cell-penetrating peptides by feature

Xiaoli Qiang1, Chen Zhou2, Xiucai Ye3

  • 1Institute of Computing Science and Technology, Guangzhou University, Guangzhou, China.

Briefings in Bioinformatics
|September 22, 2018
PubMed
Summary

CPPred-FL accurately identifies cell-penetrating peptides (CPPs) for drug delivery. This bioinformatics tool uses a novel feature learning scheme for enhanced prediction of CPPs, advancing therapeutic applications.

Keywords:
cell-penetrating peptidefeature representation learningmachine learningsequence analysis

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Drug Delivery Systems

Background:

  • Cell-penetrating peptides (CPPs) are crucial for intracellular cargo delivery, with significant therapeutic potential.
  • Accurate identification of CPPs is essential for understanding their mechanisms and therapeutic applications.
  • Machine learning approaches are increasingly used for CPP identification, but effective feature representation remains a challenge.

Purpose of the Study:

  • To develop a powerful bioinformatics tool, CPPred-FL, for fast, accurate, and large-scale identification of CPPs.
  • To introduce a novel feature representation learning scheme to improve predictive performance by exploiting CPP characteristics.
  • To optimize feature selection for enhanced predictive accuracy and efficiency.

Main Methods:

  • Developed CPPred-FL, a tool integrating 45 random forest models with diverse feature descriptors (compositional, positional, physicochemical).
  • Implemented a feature representation learning scheme incorporating class and probabilistic information.
  • Performed feature space optimization to remove redundant features, utilizing 19 informative features.

Main Results:

  • CPPred-FL demonstrated superior performance compared to state-of-the-art predictors in benchmarking experiments.
  • The novel feature representation learning scheme effectively captured essential CPP characteristics.
  • Feature selection resulted in a highly efficient model using only 19 informative features.

Conclusions:

  • CPPred-FL is a highly effective tool for large-scale CPP identification.
  • The developed feature representation and selection methods significantly enhance prediction accuracy.
  • CPPred-FL will accelerate CPP characterization and their clinical therapeutic applications.