化学
内吞作用
荧光
锚固
细胞
癌细胞
膜
生物物理学
细胞生物学
癌症
纳米技术
生物化学
量子力学
结构工程
医学
生物
物理
内科学
工程类
材料科学
作者
Xin Peng,Chuixi Kong,Shuyi Jiang,Yingye Weng,Xinyue Shi,Hui Feng,Weidong Liu,Jin Zhou,Zhigang Jin,Zhaosheng Qian
标识
DOI:10.1021/acs.analchem.5c01629
摘要
Endocytosis plays a critical role in regulating protein dynamics, and cancer cells often exploit this process to enhance their survival capacity. However, the development of reliable tools for high-fidelity visualization of endocytosis under cellular stress remains a significant challenge. In this study, we introduce a fluorescent probe, o-IP-IP, based on a dimeric dual-anchoring strategy, to investigate plasma membrane dynamics and endocytosis processes. The probe incorporates two alkyl chains for targeted binding to the plasma membrane while maintaining water solubility through two negatively charged units. This design enables o-IP-IP to exhibit target-activated fluorescence enhancement, broad applicability across various cell types, and the ability to distinguish between normal and cancerous cells based on membrane viscosity. The probe's dual anchoring minimizes passive transport-induced internalization, allowing prolonged labeling of the plasma membrane and enabling high-fidelity imaging of both membranes and endocytosis processes under endocytosis inhibition. This feature facilitated real-time observation of endocytosis in living cells under osmotic stress. Furthermore, o-IP-IP enabled visualization of endocytosis induced by different extracellular calcium ion concentrations, confirming its utility as a simple and effective tool for high-fidelity endocytosis tracking in cellular stress and cell death studies. The probe was also applied to study dynamic surface protein distribution under specific external stress, highlighting endocytosis as the dominant mechanism for adjusting surface proteins. These findings underscore endocytosis' central role in maintaining cellular homeostasis and provide effective strategies for designing targeted probes and drugs based on membrane-impermeable substances' endocytosis mechanisms.
科研通智能强力驱动
Strongly Powered by AbleSci AI