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 |
| 卷 | 12 |
| 期 | 5 |
| DOI | |
| 出版状态 | 已出版 - 16 1月 2024 |
| 已对外发布 | 是 |
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:
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可持续发展目标 3 良好健康与福祉
指纹
探究 'Intranuclear assembly of leucine-rich peptides for selective death of osteosarcoma cells' 的科研主题。它们共同构成独一无二的指纹。引用此
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