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铼(I)配合物作为原核细胞和真菌细胞的荧光显微镜探针:配体重要吗?

Rhenium (I) Complexes as Probes for Prokaryotic and Fungal Cells by Fluorescence Microscopy: Do Ligands Matter?

作者信息

Otero Carolina, Carreño Alexander, Polanco Rubén, Llancalahuen Felipe M, Arratia-Pérez Ramiro, Gacitúa Manuel, Fuentes Juan A

机构信息

Facultad de Medicina, Escuela de Química y Farmacia, Universidad Andres Bello, Santiago, Chile.

Center for Applied Nanosciences (CANS), Universidad Andres Bello, Santiago, Chile.

出版信息

Front Chem. 2019 Jun 26;7:454. doi: 10.3389/fchem.2019.00454. eCollection 2019.

DOI:10.3389/fchem.2019.00454
PMID:31297366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6606945/
Abstract

Re(I) complexes have exposed highly suitable properties for cellular imaging (especially for fluorescent microscopy) such as low cytotoxicity, good cellular uptake, and differential staining. These features can be modulated or tuned by modifying the ligands surrounding the metal core. However, most of Re(I)-based complexes have been tested for non-walled cells, such as epithelial cells. In this context, it has been proposed that Re(I) complexes are inefficient to stain walled cells (i.e., cells protected by a rigid cell wall, such as bacteria and fungi), presumably due to this physical barrier hampering cellular uptake. More recently, a series of studies have been published showing that a suitable combination of ligands is useful for obtaining Re(I)-based complexes able to stain walled cells. This review summarizes the main characteristics of different fluorophores used in bioimage, remarking the advantages of d-based complexes, and focusing on Re(I) complexes. In addition, we explored different structural features of these complexes that allow for obtaining fluorophores especially designed for walled cells (bacteria and fungi), with especial emphasis on the ligand choice. Since many pathogens correspond to bacteria and fungi (yeasts and molds), and considering that these organisms have been increasingly used in several biotechnological applications, development of new tools for their study, such as the design of new fluorophores, is fundamental and attractive.

摘要

铼(I)配合物具有非常适合细胞成像(尤其是荧光显微镜成像)的性质,如低细胞毒性、良好的细胞摄取和差异染色。这些特性可以通过修饰金属核心周围的配体来调节或调整。然而,大多数基于铼(I)的配合物已针对非壁细胞(如上皮细胞)进行了测试。在这种情况下,有人提出铼(I)配合物对壁细胞(即受刚性细胞壁保护的细胞,如细菌和真菌)染色效率低下,推测是由于这种物理屏障阻碍了细胞摄取。最近,一系列研究表明,配体的适当组合有助于获得能够对壁细胞染色的基于铼(I)的配合物。本综述总结了生物成像中使用的不同荧光团的主要特征,阐述了基于d的配合物的优点,并重点关注铼(I)配合物。此外,我们探讨了这些配合物的不同结构特征,这些特征有助于获得专门为壁细胞(细菌和真菌)设计的荧光团,特别强调了配体的选择。由于许多病原体对应于细菌和真菌(酵母和霉菌),并且考虑到这些生物体在多种生物技术应用中越来越多地被使用,开发用于研究它们的新工具,如新荧光团的设计,是至关重要且有吸引力的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9e/6606945/26efe325999d/fchem-07-00454-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9e/6606945/7402a37374df/fchem-07-00454-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9e/6606945/26efe325999d/fchem-07-00454-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9e/6606945/7402a37374df/fchem-07-00454-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9e/6606945/26efe325999d/fchem-07-00454-g0002.jpg

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