State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, and ‡State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University , Nanjing 210023, China.
Anal Chem. 2017 Sep 19;89(18):9911-9917. doi: 10.1021/acs.analchem.7b02147. Epub 2017 Sep 1.
Single cell analysis is essential for understanding the heterogeneity, behaviors of cells, and diversity of target analyte in different subcellular regions. Nucleolin (NCL) is a multifunctional protein that is markedly overexpressed in most of the cancer cells. The variant expression levels of NCL in subcellular regions have a marked influence on cancer proliferation and treatments. However, the specificity of available methods to identify the cancer biomarkers is limited because of the high level of subcellular matrix effect. Herein, we proposed a novel technique to increase both the molecular and spectral specificity of cancer diagnosis by using aptamers affinity based portable nanopipette with distinctive surface-enhanced Raman scattering (SERS) activities. The aptamers-functionalized gold-coated nanopipette was used to capture target, while p-mercaptobenzonitrile (MBN) and complementary DNA modified Ag nanoparticles (AgNPs) worked as Raman reporter to produce SERS signal. The SERS signal of Raman nanotag was lost upon NCL capturing via modified DNA aptamers on nanoprobe, which further helped to verify the specificity of nanoprobe. For proof of concept, NCL protein was specifically extracted from different cell lines by aptamers modified SERS active nanoprobe. The nanoprobes manifested specifically good affinity for NCL with a dissociation constant K of 36 nM and provided a 1000-fold higher specificity against other competing proteins. Furthermore, the Raman reporter moiety has a vibrational frequency in the spectroscopically silent region (1800-2300 cm) with a negligible matrix effect from cell analysis. The subcellular localization and spatial distribution of NCL were successfully achieved in various types of cells, including MCF-7A, HeLa, and MCF-10A cells. This type of probing technique for single cell analysis could lead to the development of a new perspective in cancer diagnosis and treatment at the cellular level.
单细胞分析对于理解细胞异质性、行为和不同亚细胞区域中目标分析物的多样性至关重要。核仁素 (NCL) 是一种多功能蛋白,在大多数癌细胞中明显过表达。NCL 在亚细胞区域中的变异表达水平对癌症增殖和治疗有显著影响。然而,由于亚细胞基质效应水平高,现有方法识别癌症生物标志物的特异性有限。在此,我们提出了一种新的技术,通过使用具有独特表面增强拉曼散射 (SERS) 活性的适配体亲和力便携式纳米移液器来提高癌症诊断的分子和光谱特异性。适配体功能化的金涂层纳米移液器用于捕获靶标,而 p-巯基苯甲腈 (MBN) 和互补 DNA 修饰的 Ag 纳米颗粒 (AgNPs) 则作为拉曼报告分子产生 SERS 信号。通过纳米探针上修饰的 DNA 适配体捕获靶标后,Raman nanotag 的 SERS 信号丢失,这进一步有助于验证纳米探针的特异性。为了验证概念,通过适配体修饰的 SERS 活性纳米探针从不同细胞系中特异性提取 NCL 蛋白。纳米探针对 NCL 表现出特异性的高亲和力,解离常数 K 为 36 nM,对其他竞争蛋白的特异性提高了 1000 倍。此外,拉曼报告分子部分在光谱上处于静默区域(1800-2300 cm)具有振动频率,细胞分析的基质效应可忽略不计。成功实现了 NCL 在各种类型细胞中的亚细胞定位和空间分布,包括 MCF-7A、HeLa 和 MCF-10A 细胞。这种单细胞分析的探测技术可能为癌症诊断和细胞水平治疗开辟新视角。