Kilic Tugba, Cho Young Kwan, Jeong Naebong, Shin Ik-Soo, Carter Bob S, Balaj Leonora, Weissleder Ralph, Lee Hakho
Center for Systems Biology, Massachusetts General Hospital, Boston, Massachusetts 02114, United States.
Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, United States.
ACS Cent Sci. 2022 Jan 26;8(1):110-117. doi: 10.1021/acscentsci.1c01193. Epub 2022 Jan 7.
Detecting protein markers in extracellular vesicles (EVs) is becoming a useful tool for basic research and clinical diagnoses. Most EV protein assays, however, require lengthy processes-conjugating affinity ligands onto sensing substrates and affixing EVs with additional labels to maximize signal generation. Here, we present an iPEX (impedance profiling of extracellular vesicles) system, an all-electrical strategy toward fast, multiplexed EV profiling. iPEX adopts one-step electropolymerization to rapidly functionalize sensor electrodes with antibodies; it then detects EV proteins in a label-free manner through impedance spectroscopy. The approach streamlines the entire EV assay, from sensor preparation to signal measurements. We achieved (i) fast immobilization of antibodies (<3 min) per electrode; (ii) high sensitivity (500 EVs/mL) without secondary labeling; and (iii) parallel detection (quadruple) in a single chip. A potential clinical utility was demonstrated by directly analyzing plasma samples from glioblastoma multiforme patients.
检测细胞外囊泡(EVs)中的蛋白质标志物正成为基础研究和临床诊断的一项有用工具。然而,大多数EV蛋白质检测需要冗长的过程——将亲和配体缀合到传感底物上,并给EVs附加标签以最大化信号产生。在此,我们展示了一种iPEX(细胞外囊泡阻抗分析)系统,这是一种用于快速、多重EV分析的全电学策略。iPEX采用一步电聚合来用抗体快速功能化传感器电极;然后它通过阻抗谱以无标记方式检测EV蛋白质。该方法简化了从传感器制备到信号测量的整个EV检测过程。我们实现了:(i)每个电极快速固定抗体(<3分钟);(ii)无需二次标记的高灵敏度(500个EVs/毫升);以及(iii)在单个芯片中进行平行检测(四重)。通过直接分析多形性胶质母细胞瘤患者的血浆样本证明了其潜在的临床应用价值。