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基于适配体的夹心测定法及其在检测肝细胞癌(HCC)中脂联素-2的临床前景。

Aptamer-based Sandwich Assay and its Clinical Outlooks for Detecting Lipocalin-2 in Hepatocellular Carcinoma (HCC).

作者信息

Lee Kyeong-Ah, Ahn Ji-Young, Lee Sang-Hee, Singh Sekhon Simranjeet, Kim Dae-Ghon, Min Jiho, Kim Yang-Hoon

机构信息

Department of Microbiology, Chungbuk National University, 1 Chungdae-Ro, Seowon-Gu, Cheongju 362-763, South Korea.

Division of Gastroenterology and Hepatology, Research Institute of Clinical Medicine, Department of Internal Medicine, Chonbuk National University, Medical School and Hospital, Jeonju, 561-756, South Korea.

出版信息

Sci Rep. 2015 Jun 3;5:10897. doi: 10.1038/srep10897.

Abstract

We validated a single-stranded, DNA aptamer-based, diagnostic method capable of detecting Lipocalin-2 (LCN2), a biomarker from clinically relevant hepatocellular carcinoma (HCC) patient serum, in the sandwich assay format. Nine aptamers (LCN2_apta1 to LCN2_apta9) for LCN2 were screened with SELEX processes, and a sandwich pair (LCN2_apta2 and LCN2_apta4) was finally chosen using surface plasmon resonance (SPR) and dot blotting analysis. The result of the proposed aptamer sandwich construction shows that LCN2 was sensitively detected in the concentration range of 2.5-500 ng mL(-1) with a limit of detection of 0.6 ng mL(-1). Quantitative measurement tests in HCC patients were run on straight serum and were compared with the performance of the conventional antibody-based ELISA kit. The aptamer sandwich assay demonstrated an excellent dynamic range for LCN2 at clinically relevant serum levels, covering sub-nanogram per mL concentrations. The new approach offers a simple and robust method for detecting serum biomarkers that have low and moderate abundance. It consists of functionalization, hybridization and signal read-out, and no dilution is required. The results of the study demonstrate the capability of the aptamer sandwich assay platform for diagnosing HCC and its potential applicability to the point-of-care testing (POCT) system.

摘要

我们验证了一种基于单链DNA适配体的诊断方法,该方法能够以夹心检测法检测来自临床相关肝细胞癌(HCC)患者血清的生物标志物脂蛋白2(LCN2)。通过指数富集的配体系统进化技术(SELEX)筛选出9种针对LCN2的适配体(LCN2_apta1至LCN2_apta9),并最终通过表面等离子体共振(SPR)和斑点印迹分析选择了一对夹心适配体(LCN2_apta2和LCN2_apta4)。所提出的适配体夹心结构的检测结果表明,在2.5 - 500 ng mL⁻¹的浓度范围内能够灵敏地检测到LCN2,检测限为0.6 ng mL⁻¹。对HCC患者的血清进行直接定量检测,并与传统基于抗体的ELISA试剂盒的性能进行比较。适配体夹心检测法在临床相关血清水平下对LCN2显示出优异的动态范围,涵盖每毫升亚纳克浓度。这种新方法为检测低丰度和中等丰度的血清生物标志物提供了一种简单而稳健的方法。它包括功能化、杂交和信号读出,无需稀释。研究结果证明了适配体夹心检测平台在诊断HCC方面的能力及其在即时检测(POCT)系统中的潜在适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917f/4454046/948cc1fa5a8a/srep10897-f1.jpg

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