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Intranuclear assembly of leucine-rich peptides for selective death of osteosarcoma cells

  • Shuang Liu*
  • , Qiuxin Zhang
  • , Xingrao Peng
  • , Cong Hu
  • , Shaowei Wang*
  • , Yao Sun*
  • *Corresponding author for this work
  • Wuhan University of Technology
  • CAS - Shanghai Institute of Technical Physics
  • Brandeis University
  • Central China Normal University
  • Guilin University of Electronic Technology

Research output: Contribution to journalArticlepeer-review

Abstract

Herein, we show a pair of leucine-rich l- and d-phosphopeptides which self-assemble into twisting nanofibers, whose secondary structures contain a strong β-sheet component after being dephosphorylated by alkaline phosphatase (ALP). While being incubated with ALP overexpressing osteosarcoma cells, both of the peptides self-assemble in the nuclei and induce cell death. The cell death involves multiple cell death modalities and occurs along with the disruption of cell membranes. Enzyme-instructed self-assembly (EISA) inhibits osteosarcoma cells and shows no side effect to other cells. In addition, the cancer cells hardly gain drug resistance after repeated treatment. This work reports a pair of EISA-based nanofibers to target cell nuclei, and also provides a novel chemotherapeutic agent to inhibit osteosarcoma cells without side effects and drug resistance.

Original languageEnglish
Pages (from-to)1274-1280
Number of pages7
JournalBiomaterials Science
Volume12
Issue number5
DOIs
StatePublished - 16 Jan 2024
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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