Department of Surgery, Division of Surgical Research, Mayo Clinic, Rochester, MN 55905, USA.
Microbiome Program, Center for Individualized Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Biosensors (Basel). 2022 Feb 9;12(2):104. doi: 10.3390/bios12020104.
Extracellular vesicles (EVs) have gained considerable attention as vital circulating biomarkers since their structure and composition resemble the originating cells. The investigation of EVs' biochemical and biophysical properties is of great importance to map them to their parental cells and to better understand their functionalities. In this study, a novel frequency-dependent impedance measurement system has been developed to characterize EVs based on their unique dielectric properties. The system is composed of an insulator-based dielectrophoretic (iDEP) device to entrap and immobilize a cluster of vesicles followed by utilizing electrical impedance spectroscopy (EIS) to measure their impedance at a wide frequency spectrum, aiming to analyze both their membrane and cytosolic charge-dependent contents. The EIS was initially utilized to detect nano-size vesicles with different biochemical compositions, including liposomes synthesized with different lipid compositions, as well as EVs and lipoproteins with similar biophysical properties but dissimilar biochemical properties. Moreover, EVs derived from the same parental cells but treated with different culture conditions were characterized to investigate the correlation of impedance changes with biochemical properties and functionality in terms of pro-inflammatory responses. The system also showed the ability to discriminate between EVs derived from different cellular origins as well as among size-sorted EVs harbored from the same cellular origin. This proof-of-concept approach is the first step towards utilizing EIS as a label-free, non-invasive, and rapid sensor for detection and characterization of pathogenic EVs and other nanovesicles in the future.
细胞外囊泡 (EVs) 因其结构和组成与起源细胞相似,已成为重要的循环生物标志物而备受关注。研究 EVs 的生化和物理特性对于将其映射到其亲本细胞并更好地理解其功能非常重要。在这项研究中,开发了一种新型的基于频率的阻抗测量系统,该系统基于其独特的介电特性来表征 EVs。该系统由基于绝缘体的介电泳 (iDEP) 装置组成,用于捕获和固定一组囊泡,然后利用阻抗谱 (EIS) 测量其在宽频谱范围内的阻抗,旨在分析其膜和细胞质电荷依赖性内容物。EIS 最初用于检测具有不同生化组成的纳米级囊泡,包括用不同脂质组成合成的脂质体,以及具有相似物理特性但生化特性不同的 EVs 和脂蛋白。此外,还对源自相同亲本细胞但经过不同培养条件处理的 EVs 进行了表征,以研究阻抗变化与炎症反应等生化特性和功能之间的相关性。该系统还显示了区分源自不同细胞来源的 EVs 以及源自同一细胞来源的大小分选 EVs 的能力。这种概念验证方法是将来利用 EIS 作为无标记、非侵入性和快速传感器来检测和表征致病 EVs 和其他纳米囊泡的第一步。