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基于新型 SALDI-MS 靶的血清脂质高覆盖率检测的双机制驱动策略。

Dual-Mechanism-Driven Strategy for High-Coverage Detection of Serum Lipids on a Novel SALDI-MS Target.

机构信息

Institute of Analytical Chemistry, Department of Chemistry, Zhejiang University, Hangzhou 310058, China.

Department of General Surgery, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310016, China.

出版信息

Anal Chem. 2022 Jun 21;94(24):8570-8579. doi: 10.1021/acs.analchem.1c04929. Epub 2022 Jun 7.

Abstract

Serum lipid metabolites have been emerging as ideal biomarkers for disease diagnosis and prediction. In the current stage, nontargeted or targeted lipidomic research mainly relies on a liquid chromatography-mass spectrometry (LC-MS) platform, but future clinical applications need more robust and high-speed platforms. Surface-assisted laser desorption ionization mass spectrometry (SALDI-MS) has shown excellent advantages in the high-speed analysis of lipid metabolites. However, the platform in the positive ion mode is more inclined to target a certain class of lipids, leading to the low coverage of lipid detection and limiting its practical translation to clinical applications. Herein, we proposed a dual-mechanism-driven strategy for high-coverage detection of serum lipids on a novel SALDI-MS target, which is a composite nanostructure comprising vertical silicon nanowires (VSiNWs) decorated with AuNPs and polydopamine (VSiNW-Au-PDA). The performance of laser desorption and ionization on the target can be enhanced by charge-driven desorption coupled with thermal-driven desorption. Simultaneous detection of 236 serum lipids (S/N ≥ 5) including neutral and polar lipids can be achieved in the positive ion mode. Among these, 107 lipid peaks were successfully identified. When combined with VSiNW-Au-PDA and VSiNW chips, 479 lipid peaks can be detected in serum samples in positive and negative ion modes, respectively. Based on the platform, serum samples from 57 hepatocellular carcinoma (HCC) patients and 76 healthy controls were analyzed. After data mining, 14 lipids containing different lipid types (TAG, CE, PC) were selected as potential lipidomic biomarkers. With the assistance of an artificial neural network, a diagnostic model with a sensitivity of 92.7% and a specificity of 96% was constructed for HCC diagnosis.

摘要

血清脂质代谢物已成为疾病诊断和预测的理想生物标志物。在当前阶段,非靶向或靶向脂质组学研究主要依赖于液相色谱-质谱联用(LC-MS)平台,但未来的临床应用需要更强大和高速的平台。表面辅助激光解吸电离质谱(SALDI-MS)在脂质代谢物的高速分析中显示出优异的优势。然而,正离子模式下的平台更倾向于靶向某一类脂质,导致脂质检测的覆盖率较低,限制了其在临床应用中的实际转化。在此,我们提出了一种基于新型 SALDI-MS 靶标的血清脂质高覆盖率检测的双机制驱动策略,该靶标是一种由垂直硅纳米线(VSiNWs)和金纳米颗粒(AuNPs)与聚多巴胺(PDA)复合而成的纳米结构。通过电荷驱动解吸与热驱动解吸相结合,可增强靶标上的激光解吸和电离性能。可在正离子模式下同时检测 236 种血清脂质(S/N≥5),包括中性和极性脂质。其中,成功鉴定出 107 个脂质峰。当与 VSiNW-Au-PDA 和 VSiNW 芯片结合使用时,可分别在正、负离子模式下检测到血清样品中的 479 个脂质峰。基于该平台,分析了 57 例肝细胞癌(HCC)患者和 76 例健康对照者的血清样本。经过数据挖掘,选择了 14 种含有不同脂质类型(TAG、CE、PC)的脂质作为潜在的脂质组学生物标志物。在人工神经网络的辅助下,构建了一种用于 HCC 诊断的具有 92.7%灵敏度和 96%特异性的诊断模型。

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