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用于活细胞成像的溶剂化变色和 pH 敏感荧光膜探针。

Solvatochromic and pH-Sensitive Fluorescent Membrane Probes for Imaging of Live Cells.

机构信息

Department of Chemistry and Biochemistry, Florida Atlantic University, Boca Raton, Florida, United States.

Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, Florida, United States.

出版信息

ACS Chem Neurosci. 2021 Feb 17;12(4):719-734. doi: 10.1021/acschemneuro.0c00732. Epub 2021 Jan 28.

Abstract

Membrane trafficking is essential for all cells, and visualizing it is particularly useful for studying neuronal functions. Here we report the synthesis, characterization, and application of several membrane- and pH-sensitive probes suitable for live-cell fluorescence imaging. These probes are based on a 1,8-naphthalimide fluorophore scaffold. They exhibit a solvatochromic effect, and one of them, ND6, shows a substantial fluorescence difference between pH 6 and 7. The solvatochromic effect and pH-sensitivity of those probes are explained using quantum chemical calculations, and molecular dynamics simulation confirms their integration and interaction with membrane lipids. For live-cell fluorescence imaging, we tested those probes in a cancer cell line (MCF7), cancer spheroids (MDA-MB-468), and cultured hippocampal neurons. Confocal imaging showed an excellent signal-to-noise ratio from 400:1 to about 1300:1 for cell membrane labeling. We applied ND6 during stimulation to label nerve terminals via dye uptake during evoked synaptic vesicle turnover. By ND6 imaging, we revealed cholesterol's multifaced role in replenishing synaptic vesicle pools. Our results demonstrate these fluorescent probes' great potential in studying membrane dynamic and synaptic functions in neurons and other secretory cells and tissues.

摘要

膜转运对于所有细胞都是必不可少的,而对其进行可视化特别有助于研究神经元功能。在这里,我们报告了几种适合用于活细胞荧光成像的膜和 pH 敏感探针的合成、表征和应用。这些探针基于 1,8-萘二甲酰亚胺荧光团支架。它们表现出溶剂化变色效应,其中一种探针 ND6 在 pH 6 和 7 之间表现出显著的荧光差异。使用量子化学计算解释了这些探针的溶剂化变色效应和 pH 敏感性,分子动力学模拟证实了它们与膜脂的整合和相互作用。对于活细胞荧光成像,我们在癌细胞系(MCF7)、癌细胞球体(MDA-MB-468)和培养的海马神经元中测试了这些探针。共聚焦成像显示,细胞膜标记的信噪比从 400:1 到约 1300:1 非常好。我们在刺激期间应用 ND6 通过摄取染料来标记神经末梢,以标记诱发的突触小泡翻转期间的神经末梢。通过 ND6 成像,我们揭示了胆固醇在补充突触小泡库中的多方面作用。我们的结果表明,这些荧光探针在研究神经元和其他分泌细胞和组织中的膜动态和突触功能方面具有巨大的潜力。

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