高尔基体
细胞器
细胞生物学
癌细胞
分泌物
内体
纤维
化学
材料科学
纳米生物技术
毛皮
生物物理学
纳米技术
生物
内质网
细胞
癌症
生物化学
纳米颗粒
酶
遗传学
作者
Rong Sheng Li,Jiahui Liu,Hu Shi,Ping Ping Hu,Yao Wang,Peng Fei Gao,Jian Wang,Moye Jia,Hongwei Li,Yuan Fang Li,Chengde Mao,Na Li,Cheng Zhi Huang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-09-27
卷期号:21 (19): 8455-8465
被引量:29
标识
DOI:10.1021/acs.nanolett.1c03112
摘要
Golgi apparatus is a major subcellular organelle responsible for drug resistance. Golgi apparatus-targeted nanomechanical disruption provides an attractive approach for killing cancer cells by multimodal mechanism and avoiding drug resistance. Inspired by the poisonous twisted fibrils in Alzheimer's brain tissue and enhanced rigidity of helical structure in nature, we designed transformable peptide C6RVRRF4KY that can self-assemble into nontoxic nanoparticles in aqueous medium but transformed into left-handed helical fibrils (L-HFs) after targeting and furin cleavage in the Golgi apparatus of cancer cells. The L-HFs can mechanically disrupt the Golgi apparatus membrane, resulting in inhibition of cytokine secretion, collapse of the cellular structure, and eventually death of cancer cells. Repeated stimulation of the cancers by the precursors causes no acquired drug resistance, showing that mechanical disruption of subcellular organelle is an excellent strategy for cancer therapy without drug resistance. This nanomechanical disruption concept should also be applicable to multidrug-resistant bacteria and viruses.
科研通智能强力驱动
Strongly Powered by AbleSci AI