一种水溶性、长荧光寿命DNA探针,用于活细胞有丝分裂的实时动态可视化,并适用于FLIM/时间门控成像。

IF 6.1 3区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Kapil Kumar, Thomas Hartig Braunstein, Pablo Hernandez-Varas, Mikkel Baldtzer Liisberg and Bo W. Laursen
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引用次数: 0

摘要

用于实时监测细胞分裂的长寿命和光稳定性荧光探针,特别是用于有丝分裂和间期的动态可视化,是罕见的。我们已经开发了一种水溶性重氮杂三角铵阳离子荧光探针,nucc - daota +,符合这些标准。Nuc-DAOTA+具有很长的荧光寿命(~ 20 ns),并且专门针对活细胞中的特定DNA结合的细胞核,这对于细胞分裂(包括有丝分裂和间期)的实时动态成像至关重要。在Nuc-DAOTA+中加入dsDNA (0-50 μg mL-1)可导致吸收峰红移(~ 10 nm)和荧光峰蓝移(~ 5 nm),同时两者的强度都有所增加。荧光强度与dsDNA浓度呈极好的线性相关(R2 = 0.999),检出限为0.7 μg mL-1。利用Benesi-Hildebrand图计算Nuc-DAOTA+与DNA的结合常数为1.6 × 104 M-1,并利用CD谱分析了其结合机理。Nuc-DAOTA+具有较长的荧光寿命和良好的生物相容性,可用于共聚焦显微镜对活的CHO(中国仓鼠卵巢)细胞的有丝分裂期和间期进行实时动态成像。此外,Nuc-DAOTA+在光漂白实验中表现出较高的光稳定性,并成功应用于小鼠胚胎成纤维细胞3T3细胞系的荧光寿命成像显微镜(FLIM)和时间门控成像。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A water-soluble, long fluorescent lifetime DNA probe for real-time dynamic visualization of mitosis in live cells and applicability for FLIM/time-gated imaging

A water-soluble, long fluorescent lifetime DNA probe for real-time dynamic visualization of mitosis in live cells and applicability for FLIM/time-gated imaging

Long-lived and photostable fluorescent probes for real-time monitoring of cell division, particularly for dynamic visualization of mitosis and interphase, are rare. We have developed a water-soluble diazaoxatriangulenium cation-based fluorescent probe, Nuc-DAOTA+, that meets these criteria. Nuc-DAOTA+ has a long fluorescence lifetime (∼20 ns) and exclusively targets the nucleus for specific DNA binding in live cells, essential for real-time dynamic imaging of cell-division, including mitosis and interphase. Addition of dsDNA (0–50 μg mL−1) to Nuc-DAOTA+ results in a red shift (∼10 nm) of the absorption and a blue shift (∼5 nm) of the fluorescence maxima, along with an intensity increase in both. A very good linear correlation (R2 = 0.999) from the plot of fluorescence intensity versus concentration of dsDNA (up to 30 μg mL−1) resulted in a detection limit of 0.7 μg mL−1. The Benesi–Hildebrand plot was used to calculate the binding constant between the Nuc-DAOTA+ and DNA, which was found to be 1.6 × 104 M−1 and the mechanism of binding interactions was investigated using CD spectroscopy. The long fluorescence lifetime and excellent biocompatibility of Nuc-DAOTA+ enabled its use for real-time dynamic imaging of mitotic phases and interphase in live CHO (Chinese hamster ovary) cells by using confocal microscopy. In addition, the Nuc-DAOTA+ exhibited high photostability during photo-bleaching experiments and was successfully applied for fluorescence lifetime imaging microscopy (FLIM) and time gated imaging of the mouse embryonic fibroblast 3T3 cell line.

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来源期刊
Journal of Materials Chemistry B
Journal of Materials Chemistry B MATERIALS SCIENCE, BIOMATERIALS-
CiteScore
11.50
自引率
4.30%
发文量
866
期刊介绍: Journal of Materials Chemistry A, B & C cover high quality studies across all fields of materials chemistry. The journals focus on those theoretical or experimental studies that report new understanding, applications, properties and synthesis of materials. Journal of Materials Chemistry A, B & C are separated by the intended application of the material studied. Broadly, applications in energy and sustainability are of interest to Journal of Materials Chemistry A, applications in biology and medicine are of interest to Journal of Materials Chemistry B, and applications in optical, magnetic and electronic devices are of interest to Journal of Materials Chemistry C.Journal of Materials Chemistry B is a Transformative Journal and Plan S compliant. Example topic areas within the scope of Journal of Materials Chemistry B are listed below. This list is neither exhaustive nor exclusive: Antifouling coatings Biocompatible materials Bioelectronics Bioimaging Biomimetics Biomineralisation Bionics Biosensors Diagnostics Drug delivery Gene delivery Immunobiology Nanomedicine Regenerative medicine & Tissue engineering Scaffolds Soft robotics Stem cells Therapeutic devices
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