化学
发光
共焦显微镜
镧系元素
共焦
显微镜
荧光寿命成像显微镜
结合
荧光
荧光显微镜
肽
双光子激发显微术
活体细胞成像
生物物理学
细胞
材料科学
光学
生物化学
光电子学
离子
数学分析
物理
生物
有机化学
数学
作者
Ji-Hyung Choi,Guillaume Fremy,Thibault Charnay,Nour Fayad,Jacques Pécaut,Sule Erbek,Niko Hildebrandt,Véronique Martel-Frachet,Alexeï Grichine,Olivier Sénèque
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2022-12-07
卷期号:61 (50): 20674-20689
被引量:3
标识
DOI:10.1021/acs.inorgchem.2c03646
摘要
Lanthanide(III) (Ln3+) complexes feature desirable luminescence properties for cell microscopy imaging, but cytosolic delivery of Ln3+ complexes and their use for 2P imaging of live cells are challenging. In this article, we describe the synthesis and spectroscopic characterizations of a series of Ln3+ complexes based on two ligands, L1 and L2, featuring extended picolinate push-pull antennas for longer wavelength absorption and 2P absorption properties as well as a free carboxylate function for conjugation to peptides. Several cell penetrating peptide/Ln3+ complex conjugates were then prepared with the most interesting luminescent complexes, Tb(L1) and Eu(L2), and with two cell penetrating peptides (CPPs), ZF5.3 and TP2. A spectroscopic analysis demonstrates that the luminescence properties of the complexes are not affected by conjugation to the peptide. The conjugates were evaluated for one-photon (1P) time-gated microscopy imaging, which suppresses biological background fluorescence, and 2P confocal microscopy. Whereas TP2-based conjugates were unable to enter cells, successful 1P and 2P imaging was performed with ZF5.3[Tb(L1)]. 2P confocal imaging suggests proper internalization and cytosolic delivery as expected for this CPP. Noteworthy, 2P confocal microscopy also allowed characterization of the luminescence properties of the complex (spectrum, lifetime) within the cell, opening the way to functional luminescent probes for 2P confocal imaging of live cells.
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