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基于荧光测定的活细胞凋亡成像用细胞膜包覆的金纳米粒子

Cell membrane-coated gold nanoparticles for apoptosis imaging in living cells based on fluorescent determination.

机构信息

Center for Molecular Recognition and Biosensing, School of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.

Shanghai Key Laboratory of Bio-Energy Crop, School of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China.

出版信息

Mikrochim Acta. 2020 Feb 18;187(3):175. doi: 10.1007/s00604-020-4130-1.

Abstract

A nanoprobe was developed to achieve apoptosis detection by cell membrane-functionalized gold nanoparticles (AuNP-pep@Mem). The fluorescence of the fluorescein isothiocyanate isomer I (FITC)-labeled caspase-3 substrates was quenched by the attachment to AuNPs. The fluorescence signal was recovered via the cleavage of caspase-3 under apoptotic conditions. It exhibited a low detection limit of 1.3 pg·mL with a linear range from 3.2 to 100 pg·mL for caspase-3 detection with excitation wavelength of 490 nm. After wrapped by the cell membrane, the nanoprobe was effectively delivered into cells with high cell permeability. AuNP-pep@Mem nanoprobe provided signal enhancement of 1.8 times in living cells compared to non-membrane-coated nanoparticles (AuNP-pep). In combination with its excellent stability, low LOD and good specificity, the AuNP-pep@Mem probe can be an ideal probe for fluorescence imaging of apoptosis. Graphical abstractSchematic representation of fluorescent determination for apoptosis in living cells based on cell membrane-coated gold nanoparticls.

摘要

一种纳米探针被开发出来,通过细胞膜功能化的金纳米粒子 (AuNP-pep@Mem) 实现细胞凋亡检测。荧光素异硫氰酸酯标记的半胱天冬酶-3 底物的荧光通过与 AuNPs 的附着而被猝灭。在凋亡条件下,通过半胱天冬酶-3 的切割恢复荧光信号。它表现出低检测限 1.3 pg·mL,对于 caspase-3 的检测,线性范围从 3.2 到 100 pg·mL,激发波长为 490nm。在被细胞膜包裹后,纳米探针具有较高的细胞通透性,有效地递送到细胞内。与非膜包裹的纳米颗粒 (AuNP-pep) 相比,AuNP-pep@Mem 纳米探针在活细胞中提供了 1.8 倍的信号增强。结合其优异的稳定性、低检测限和良好的特异性,AuNP-pep@Mem 探针可以成为用于活细胞凋亡荧光成像的理想探针。

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