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首页> 外文期刊>Angewandte Chemie >Synthesis of Fluorophores that Target Small Molecules to the Endoplasmic Reticulum of Living Mammalian Cells
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Synthesis of Fluorophores that Target Small Molecules to the Endoplasmic Reticulum of Living Mammalian Cells

机译:靶向小分子到活的哺乳动物细胞内质网的荧光团的合成。

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摘要

The endoplasmic reticulum (ER) plays critical roles in the processing of secreted and transmembrane proteins. To deliver small molecules to this organelle, we synthesized fluorinated hydrophobic analogues of the fluorophore rhodol. These cell-permeable fluorophores are exceptionally bright, with quantum yields of around 0.8, and they were found to specifically accumulate in the ER of living HeLa cells, as imaged by confocal laser scanning microscopy. To target a biological pathway controlled by the ER, we linked a fluorinated hydrophobic rhodol to 5-nitrofuran-2-acrylaldehyde. In contrast to an untargeted nitrofuran warhead, delivery of this electrophilic nitrofuran to the ER by the rhodol resulted in cytotoxicity comparable to the ER-targeted cytotoxin eeyarestatinI, and specifically inhibited protein processing by the ubiquitin-proteasome system. Fluorinated hydrophobic rhodols are outstanding fluorophores that enable the delivery of small molecules for targeting ER-associated proteins and pathways.
机译:内质网(ER)在分泌和跨膜蛋白的加工中起关键作用。为了将小分子传递到该细胞器,我们合成了荧光团rhodol的氟化疏水类似物。这些可透过细胞的荧光团异常明亮,量子产率约为0.8,并且通过共聚焦激光扫描显微镜观察发现,它们特异性地聚集在活HeLa细胞的ER中。为了靶向由ER控制的生物途径,我们将氟化的疏水性Rhodol与5-硝基呋喃-2-丙烯醛连接。与未靶向的硝基呋喃战斗部相反,这种化学亲和的硝基呋喃通过rhodol传递到ER所产生的细胞毒性与ER靶向的细胞毒素eeyarestatinI相当,并特别抑制了泛素-蛋白酶体系统的蛋白质加工。氟化疏水杜鹃花是出色的荧光团,能够递送小分子以靶向与ER相关的蛋白质和途径。

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