Kim Seokjoon, Park Ki Soo
Department of Biological Engineering, College of Engineering, Konkuk University, Seoul 05029, Republic of Korea.
Nanoscale. 2021 Jan 8;13(1):81-84. doi: 10.1039/d0nr06657e.
When imaging cells, nuclear counterstaining is imperative; however, many commercial nuclear-staining dyes based on nucleic acid intercalation result in nonspecific signals in the cytoplasm. Here, we propose a new strategy that stains the nucleus with high specificity by in situ formation of DNA-templated copper nanoparticles (CuNPs). We demonstrated that genomic DNA in the nucleus enabled rapid formation of highly fluorescent CuNPs immediately following addition of a copper ion source and ascorbate as a reducing agent. Moreover, we found that RNA and mitochondrial DNA, largely responsible for nonspecific cytoplasmic signals from commercial nuclear-staining dyes, did not mediate the formation of the highly fluorescent CuNPs, resulting in highly specific nuclear staining at a reduced cost relative to commercially available methods. Furthermore, we verified the compatibility of the proposed method with other fluorescence-labeling techniques. These results demonstrated the efficacy of this method and its promise as a powerful tool for cell imaging.
在对细胞进行成像时,细胞核复染必不可少;然而,许多基于核酸嵌入的商业核染色染料会在细胞质中产生非特异性信号。在此,我们提出一种新策略,即通过原位形成DNA模板化铜纳米颗粒(CuNP)来对细胞核进行高特异性染色。我们证明,在添加铜离子源和作为还原剂的抗坏血酸后,细胞核中的基因组DNA能够立即快速形成高荧光CuNP。此外,我们发现,商业核染色染料产生非特异性细胞质信号的主要原因——RNA和线粒体DNA,并不会介导高荧光CuNP的形成,从而以低于现有商业方法的成本实现了高特异性的细胞核染色。此外,我们验证了所提出方法与其他荧光标记技术的兼容性。这些结果证明了该方法的有效性及其作为细胞成像强大工具的潜力。