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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*
  • *此作品的通讯作者
  • Wuhan University of Technology
  • CAS - Shanghai Institute of Technical Physics
  • Brandeis University
  • Central China Normal University
  • Guilin University of Electronic Technology

科研成果: 期刊稿件文章同行评审

摘要

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.

源语言英语
页(从-至)1274-1280
页数7
期刊Biomaterials Science
12
5
DOI
出版状态已出版 - 16 1月 2024
已对外发布

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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