Side-chain-engineered fluorescent dyes for 3D and long-term dynamic tracking of the plasma membrane in living cells

IF 5.6 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2024-07-17 DOI:10.1016/j.talanta.2024.126583
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Abstract

The plasma membrane involves in many important biological events such as cell fusion and programmed cell death, but most of current plasma membrane probes cannot meet the requirement of long-term specific anchoring to the plasma membrane. Herein, we propose a molecular side-chain engineering strategy to modulate the long-term imaging performance of fluorescent dyes to the plasma membrane by regulating the cell permeability and anchoring ability. A series of FMR dyes with different lengths of side chains were designed and synthesized, and their transmembrane behaviours and staining performance were evaluated in living HeLa cells. We found that short-chain and medium-chain FMR dyes have excellent cell permeability without the labeling ability to the plasma membrane while the long-chain FMR dyes specifically stain the plasma membrane and can be firmly anchored to the plasma membrane for a long period of time. These long-chain FMR dyes have high stain specificality to the plasma membrane, and C10-FMR can be anchored to the plasma membrane of living cells for 2 h, which enables it to continuously monitor dynamic changes of the plasma membrane. The three-dimensional precision imaging of various cells was achieved using C10-FMR, which provides an opportunity to obtain complete information on the three-dimensional spatial morphology of the plasma membrane. The PEG-induced cell fusion of chicken red blood cells and H2O2-induced apoptosis of HeLa cells were monitored by real-time tracking of dynamic changes of the plasma membrane during these processes, which provide solid examples to prove the usefulness of these fluorescent dyes as long-term imaging tools. This work validates the hypothesis that cell permeability of membrane dyes can be readily regulated by tuning the side chains, and provides the effective design strategy of fluorescent dyes for 3D and long-term dynamic tracking of the plasma membrane of diverse animal cells.

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用于活细胞质膜三维和长期动态跟踪的侧链工程荧光染料。
质膜参与了许多重要的生物事件,如细胞融合和细胞程序性死亡,但目前大多数质膜探针无法满足长期特异性锚定质膜的要求。在此,我们提出了一种分子侧链工程策略,通过调节细胞通透性和锚定能力来调节荧光染料在质膜上的长期成像性能。我们设计并合成了一系列具有不同长度侧链的 FMR 染料,并在活体 HeLa 细胞中评估了它们的跨膜行为和染色性能。我们发现,短链和中链 FMR 染料具有良好的细胞渗透性,但对质膜没有标记能力;而长链 FMR 染料能特异性地染色质膜,并能长期牢固地固定在质膜上。这些长链 FMR 染料对质膜的染色特异性很高,C10-FMR 可固定在活细胞的质膜上 2 小时,从而能够连续监测质膜的动态变化。利用 C10-FMR 实现了对各种细胞的三维精密成像,从而有机会获得完整的质膜三维空间形态信息。通过实时跟踪质膜在这些过程中的动态变化,监测了 PEG 诱导的鸡红细胞融合和 H2O2- 诱导的 HeLa 细胞凋亡,为证明这些荧光染料作为长期成像工具的实用性提供了可靠的实例。这项工作验证了膜染料的细胞渗透性可通过调节侧链轻松调节的假设,并为三维和长期动态跟踪不同动物细胞质膜提供了有效的荧光染料设计策略。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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