Chen Hua-Jie, Hu Yusi, Yao Peiyu, Ning Di, Zhang Yu-Peng, Wang Zhi-Gang, Liu Shu-Lin, Pang Dai-Wen
Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, P. R. China.
State Key Laboratory of Medicinal Chemical Biology, Tianjin Key Laboratory of Biosensing and Molecular Recognition, Research Center for Analytical Sciences, College of Chemistry, and School of Medicine, Nankai University, Tianjin 300071, P. R. China.
Anal Chem. 2021 Apr 20;93(15):6128-6134. doi: 10.1021/acs.analchem.0c05322. Epub 2021 Apr 9.
Cardiovascular disease is one of the main causes of death in the world, which is closely associated with dyslipidemia. Dyslipidaemia is usually manifested as a relatively higher level of low-density lipoprotein (LDL) and lower level of high-density lipoprotein (HDL). Thus, the quantitative detection of the LDL and HDL particles is of great importance to predict the risk of cardiovascular diseases. However, the traditional methods can only indirectly reflect the HDL/LDL particle concentrations by detecting the cholesterol or proteins in HDL/LDL particles and are always laborious and time-consuming. Thus, the accurate and efficient approach for the detection of intact HDL and LDL particles is still lacking so far. We developed an enzyme- and isolation-free method to measure the concentration of HDL and LDL based on DNAzyme and hybridization chain reaction (HCR)-based signal amplification. This method can be used to directly and accurately detect the concentration of "actual" HDL and LDL particles instead of the cholesterol in HDL and LDL, with limits of detection of 10 and 30 mg/dL, respectively, which also satisfied the lipoprotein analysis in clinical samples. Therefore, this HCR-DNAzyme platform has great potential in clinical applications and health management.
心血管疾病是全球主要死因之一,与血脂异常密切相关。血脂异常通常表现为低密度脂蛋白(LDL)水平相对较高和高密度脂蛋白(HDL)水平较低。因此,定量检测LDL和HDL颗粒对于预测心血管疾病风险至关重要。然而,传统方法只能通过检测HDL/LDL颗粒中的胆固醇或蛋白质来间接反映HDL/LDL颗粒浓度,且往往费力又耗时。因此,目前仍缺乏准确、高效检测完整HDL和LDL颗粒的方法。我们基于DNAzyme和基于杂交链式反应(HCR)的信号放大技术,开发了一种无需酶和分离步骤的方法来测量HDL和LDL的浓度。该方法可直接、准确地检测“实际”HDL和LDL颗粒的浓度,而非HDL和LDL中的胆固醇,检测限分别为10和30mg/dL,这也满足了临床样本中的脂蛋白分析。因此,这个HCR-DNAzyme平台在临床应用和健康管理方面具有巨大潜力。