Key Laboratory of Optic-Electric Sensing and Analytical Chemistry for Life Science, Ministry of Education; Shandong Key Laboratory of Biochemical Analysis; Key Laboratory of Analytical Chemistry for Life Science in Universities of Shandong; and College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, PR China.
ACS Appl Mater Interfaces. 2021 Jul 21;13(28):32837-32844. doi: 10.1021/acsami.1c09388. Epub 2021 Jul 8.
Exosomes, which can transfer and deliver information about the original cell, are considered to be ideal candidates for early cancer diagnosis and evaluation of therapeutic efficacy due to their high abundance and stability. However, the highly expressed proteins on the surface of exosomes are usually associated with a variety of cancers; it is difficult to distinguish them by a single marker. Herein, a controlled self-assembly of gold nanorod (AuNR) arrays was prepared to construct a surface-enhanced Raman spectroscopy (SERS) sensor for the specific detection of exosomes secreted by SK-Br-3 cells based on a designed colocalization-dependent system (Co-DNA-Locker) and ratiometric strategy. After the exosomes are captured in the sensing array by the EpCAM aptamer modified on the surface of AuNRs, the DNA logic process occurs because the other two proteins, CD63 and HER2, are expressed simultaneously on the surface of exosomes secreted by SK-Br-3 cells, and the SERS signal intensity of the Rhodamine 6G (R6G) tagged on the terminal of DNA T increased with an increase in the concentration of the exosomes, while the SERS signal intensity of Cy5 linked on the terminal of the EpCAM aptamer, which acts as an internal standard, remains stable. The AuNRs are uniformly arranged in a hexagonal shape, and the dense "hot spots" produce "hot surfaces," which greatly improve the sensitivity and uniformity of detection. In the presence of target exosomes, the DNA colocalization three-signal input switch and the ratiometric strategy realize the specific and accurate detection of exosomes. This sensing strategy achieves a wide detection range (1.0 × 10-5.0 × 10 particles/mL) and a lower detection limit (5.3 × 10 particles/mL), without using any signal amplification mechanism, demonstrating promising applications in health care monitoring and clinical diagnostics.
外泌体可以传递和传递原始细胞的信息,由于其丰度和稳定性高,被认为是早期癌症诊断和评估治疗效果的理想候选物。然而,外泌体表面高度表达的蛋白质通常与多种癌症有关;很难用单一标志物将它们区分开来。在这里,通过设计的基于共定位的系统(Co-DNA-Locker)和比率策略,制备了金纳米棒(AuNR)阵列的受控自组装,以构建基于外泌体的表面增强拉曼光谱(SERS)传感器,用于特异性检测 SK-Br-3 细胞分泌的外泌体。在 AuNR 表面修饰的 EpCAM 适体将外泌体捕获在传感阵列中之后,由于同时在 SK-Br-3 细胞分泌的外泌体表面表达另外两种蛋白质 CD63 和 HER2,因此发生 DNA 逻辑过程,并且标记在 DNA T 末端的 Rhodamine 6G(R6G)的 SERS 信号强度随着外泌体浓度的增加而增加,而作为内参的 EpCAM 适体末端连接的 Cy5 的 SERS 信号强度保持稳定。AuNR 以六边形均匀排列,密集的“热点”产生“热表面”,大大提高了检测的灵敏度和均匀性。在存在靶向外泌体的情况下,DNA 共定位三信号输入开关和比率策略实现了对外泌体的特异性和准确检测。这种传感策略实现了宽的检测范围(1.0×10-5.0×10 个/mL)和较低的检测限(5.3×10 个/mL),而无需使用任何信号放大机制,在保健监测和临床诊断中具有广阔的应用前景。