详细信息

A multi-functional core-shell surface-enhanced Raman scattering nanosensor for simultaneous imaging of epidermal growth factor receptor on cell membranes and ROS secreted from living cells  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:A multi-functional core-shell surface-enhanced Raman scattering nanosensor for simultaneous imaging of epidermal growth factor receptor on cell membranes and ROS secreted from living cells

作者:Chen, Hua-Ying[1];Zhu, Shi-Cheng[2];Xu, Han-Bin[2];He, Yue[2];Xi, Cheng-Ye[2];Yu, Jun-Jie[2];Qian, Ruo-Can[2];Chen, Bin-Bin[2];Li, Da-Wei[2]

机构:[1]Zhejiang Shuren Univ, Coll Biol & Environm Engn, Hangzhou 310015, Peoples R China;[2]East China Univ Sci & Technol, Sch Chem & Mol Engn, Key Lab Adv Mat, Shanghai Key Lab Funct Mat Chem, Shanghai 200237, Peoples R China

年份:2025

卷号:422

外文期刊名:SENSORS AND ACTUATORS B-CHEMICAL

收录:;EI(收录号:20243817070787);WOS:【SCI-EXPANDED(收录号:WOS:001320544500001)】;

基金:This work was financially supported by the National Natural Science Foundation of China (Grant Nos. 22176058) , Science and Technology Commission of Shanghai Municipality (Grant Nos. 22ZR1416800 and 23ZR1416100) , the Program of Introducing Talents of Discipline to Universities (B16017) , the Fundamental Research Funds for the Central Universities (222201717003) , and Talent Introduction Project of Zhe-jiang Shuren University (2023R070) . The authors thank Research Center of Analysis and Test of East China University of Science and Technology for the help on the characterization.

语种:英文

外文关键词:SERS nanosensors; EGFR; ROS; Simultaneous detection; Cell imaging

摘要:The visualization of the substances on cell surface is an urgent need for the monitoring of signal transduction during intercellular communication and cancer diagnosis. Herein, a core-shell surface-enhanced Raman scattering (SERS) nanosensor is proposed for simultaneous imaging of epidermal growth factor receptor (EGFR) on cell membranes and reactive oxygen species (ROS) released from living cells. The SERS nanosensors are fabricated by embedding 4-mercaptobenzonitrile (4-MBN) molecules as a SERS tag for EGFR expression into the core-shell AuNPs@Au nanoparticles to form AuNPs@4-MBN@Au and further modifying the EGFR aptamers as EGFR recognition units and 2-mercaptohydroquinone (2-MHQ) as ROS responsive molecules on the surface of AuNPs@4-MBN@Au. Due to the specific interactions and narrow SERS peaks for spectral multiplexing, the nanosensors can target EGFR on cell membranes and achieve the SERS visualization of EGFR and ROS released from the living cells. Moreover, a positive relationship between EGFR and ROS levels on the cell membranes is revealed by using the nanosensors, showing that ROS can promote the expression of EGFR and that the high-level EGFR can facilitate the ROS generation. This ROS-promoted EGFR expression is further corroborated by western blot analysis. Overall, the proposed SERS strategy could provide a powerful tool to monitor the dynamic changes of EGFR and ROS and related signal transduction.

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