细胞质
胶体金
纳米凝胶
生物物理学
纳米技术
化学
纳米颗粒
荧光
聚合
小泡
膜
材料科学
药物输送
聚合物
生物化学
生物
物理
有机化学
量子力学
作者
Qiang Li,Fengchao Wang,Jie Yang,Dingbin Liu
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2020-03-01
卷期号:13 (3): 853-860
被引量:10
标识
DOI:10.1007/s12274-020-2707-y
摘要
Gold nanoparticles (AuNPs) assembled with fluorescent peptides through Au-S bonds (pep-AuNPs) have been widely used in biomolecular detection. However, due to the endo/lysosomal trapping after the nanoprobes enter cells, the direct delivery of AuNP probes into the cytoplasm for real-time imaging remains a difficult barrier for many cytoplasm-targeting agents. Here, we prepare AuNP@gel by wrapping a multi-functional nanogel structure on the surface of a single AuNP probe by in-situ polymerization in order to directly deliver AuNP probes into the cell cytoplasm. Compared with the pep-AuNP probes, which are trapped inside lysosomes for long periods, the AuNP@gel probes use the proton-sponge effect to effectively disrupt endo/lysosomal membranes and remain in the cytoplasm. In addition, the AuNP@gel probes rapidly escape from endo/lysosomes to avoid the complex environment that interferes with the stability of the AuNP probes and the lysosomal-storage trigger the upregulation of oxidative stress into the cells. The nanogel structure enables the AuNP probes to avoid some detrimental effects and to achieve high-fidelity fluorescence signals in the cells. Compared to traditional strategies for lysosomal escape, this one-step in-situ polymerization procedure avoids the complicated modification of additional ligands and is generally applicable to peptide-, DNA-, and polymerlinked AuNP probes.
科研通智能强力驱动
Strongly Powered by AbleSci AI