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用于聚集诱导发光/自组装导向(生物)成像的高发射蒽缔合物激基复合物的形成。

Formation of Highly Emissive Anthracene Excimers for Aggregation-Induced Emission/Self-Assembly Directed (Bio)imaging.

机构信息

Unidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.

Centro Regional de Investigaciones Biomédicas (CRIB), 02008 Albacete, Spain.

出版信息

ACS Appl Mater Interfaces. 2023 Sep 27;15(38):44786-44795. doi: 10.1021/acsami.3c10823. Epub 2023 Sep 12.

Abstract

AIEgens have emerged as a promising alternative to molecular rotors in bioimaging applications. However, transferring the concept of aggregation-induced emission (AIE) from solution to living systems remains a challenge. Given the highly heterogeneous nature and the compartmentalization of the cell, different approaches are needed to control the self-assembly within the crowded intricate cellular environment. Herein, we report for the first time the self-assembly mechanism of an anthracene-guanidine derivative (AG) forming the rare and highly emissive T-shaped dimer in breast cancer cell lines as a proof of concept. This process is highly sensitive to the local environment in terms of polarity, viscosity, and/or water quantity that should enable the use of the AG as a fluorescence lifetime imaging biosensor for intracellular imaging of cellular structures and the monitoring of intracellular state parameters. Different populations of the monomer and T-shaped and π-π dimers were observed in the cell membrane, cytoplasm, and nucleoplasm, related to the local viscosity and presence of water. The T-shaped dimer is formed preferentially in the nucleus because of the higher density and viscosity compared to the cytoplasm. The present results should serve as a precursor for the development of new design strategies for molecular systems for a wide range of applications such as cell viscosity, density, or temperature sensing and imaging.

摘要

AIEgens 已成为生物成像应用中分子转子的一种有前途的替代品。然而,将聚集诱导发光 (AIE) 的概念从溶液转移到活系统仍然是一个挑战。鉴于细胞的高度异质性和分隔性,需要采用不同的方法来控制在拥挤复杂的细胞环境中进行的自组装。在此,我们首次报道了蒽胍衍生物 (AG) 的自组装机制,该机制在乳腺癌细胞系中形成罕见的高发光 T 型二聚体,以此作为概念验证。这个过程对极性、粘度和/或水量等局部环境非常敏感,这应该使 AG 能够作为荧光寿命成像生物传感器,用于细胞内结构的成像和细胞内状态参数的监测。在细胞膜、细胞质和核质中观察到单体和 T 型和 π-π 二聚体的不同群体,这与局部粘度和水的存在有关。由于与细胞质相比,核内的密度和粘度更高,因此 T 型二聚体优先在核内形成。本研究结果应该为开发用于广泛应用的分子系统的新设计策略提供了基础,例如细胞粘度、密度或温度传感和成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4d6/11165449/828e88b77ad4/am3c10823_0002.jpg

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