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通过近红外七甲川菁染料骨架的微小变化发现靶向线粒体 G-四链体的荧光配体。

Discovery of a mitochondrial G-quadruplex targeted fluorescent ligand via a slight variation on the near-infrared heptamethine cyanine scaffold.

机构信息

Nation-Regional Engineering Lab for Synthetic Biology of Medicine, International Cancer Center, School of Pharmacy, Shenzhen University Medical School, Shenzhen 518060, China.

Nation-Regional Engineering Lab for Synthetic Biology of Medicine, International Cancer Center, School of Pharmacy, Shenzhen University Medical School, Shenzhen 518060, China.

出版信息

Int J Biol Macromol. 2024 Jun;269(Pt 2):132230. doi: 10.1016/j.ijbiomac.2024.132230. Epub 2024 May 8.

DOI:10.1016/j.ijbiomac.2024.132230
PMID:38729485
Abstract

The heptamethine cyanine dyes are one kind of promising near-infrared (NIR) compounds, holding great potential in both diagnostic and therapeutic regions. Remolding such structures to realize detection of unclarified biotargets or interfering with them seems to be important in the field of chemical biology. In this study, we developed a fluorescent ligand (IR1) targeting mitochondrial G-quadruplexes (mitoG4s) by a slight variation on the typical NIR scaffold (IR780). This ligand could be applied for sensing mitoG4s by fluorescence, making it different from the unmodified dye whose fluorescence was quenched by mitoG4s. Then, IR1 was demonstrated to accumulate in the mitochondria through a mitochondrial membrane potential (MMP) dependent manner. Some of IR1 then bound to mitoG4s, causing mtDNA loss and mitochondrial dysfunction, which thereby triggered PANoptosis, including apoptosis, autophagy and pyroptosis. To the best of our knowledge, IR1 was the first NIR fluorescent ligand with emission centered at above 800 nm for mitoG4s, and the first example causing PANoptosis among the reported mitoG4-targeted ligands.

摘要

七甲川花菁染料是一类很有前途的近红外(NIR)化合物,在诊断和治疗领域都有很大的潜力。对这些结构进行改造,以实现对未阐明的生物靶标的检测或对其进行干扰,在化学生物学领域似乎很重要。在这项研究中,我们通过对典型的 NIR 支架(IR780)进行轻微的改变,开发了一种靶向线粒体 G-四链体(mitoG4s)的荧光配体(IR1)。该配体可以通过荧光来检测 mitoG4s,与未修饰的染料不同,后者的荧光被 mitoG4s 猝灭。然后,IR1 被证明可以通过线粒体膜电位(MMP)依赖的方式在线粒体中积累。然后,一部分 IR1 与 mitoG4s 结合,导致 mtDNA 丢失和线粒体功能障碍,从而引发 PANoptosis,包括细胞凋亡、自噬和细胞焦亡。据我们所知,IR1 是第一个发射波长在 800nm 以上的近红外荧光配体,也是报道的 mitoG4 靶向配体中第一个引发 PANoptosis 的配体。

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