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用于无创检测细胞外囊泡中血管内皮钙黏蛋白的功能化丝网印刷电极。

Functionalized screen-printed electrodes for non-invasive detection of vascular-endothelial cadherin in extracellular vesicles.

作者信息

Meza-Morales William, Ayus-Martinez Sahimy, Jimenez-Osorio Jesus, Buendia-Otero Maria, López Luis, Suleiman David, Suarez Edu, Freytes Donald O, Cunci Lisandro, Mora Camilo

机构信息

Department of Chemical Engineering, University of Puerto Rico-Mayaguez Route 108 Mayaguez Puerto Rico USA

Department of Chemistry, University of Puerto Rico-Rio Piedras 601 Av. Universidad San Juan Puerto Rico USA.

出版信息

RSC Adv. 2025 Apr 22;15(16):12609-12621. doi: 10.1039/d4ra08926j. eCollection 2025 Apr 16.

Abstract

In this study, we developed a biosensor using a gold screen-printed electrode (Au-SPE) functionalized with mercaptoundecanoic acid (MUA) and an antibody for detecting the vascular-endothelial cadherin (CD144) as a endothelial biomarker protein on extracellular vesicles (EVs) isolated from saliva. The MUA functionalization provides a stable platform for immobilizing the CD144 antibody, ensuring the detection of the target protein. This biosensor combines Au-SPE technology with an immunoassay, offering a rapid, sensitive, and non-invasive method for detection of CD144 carried by EVs. Characterization of saliva-derived EVs using transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA) confirmed their morphology and size, which fell within the expected range of 80-180 nm. NTA indicated a lower concentration of particles in saliva-EVs than in serum-EVs (controls), highlighting the need for sensitive detection of EV cargos in this type of EV. Immunodetection confirmed the presence of CD144 in both saliva and serum-derived EVs, with higher concentrations in serum. Functionalization of Au-SPEs with MUA and CD144 antibodies was confirmed by significant resistance changes, and atomic force microscopy (AFM) was used to verify the preservation of EV morphology and their capturing post-immune adsorption. A calibration curve demonstrated the high sensitivity of the biosensor prototype for detecting CD144-positive EVs, with a limit of detection (LOD) of 0.111 ng mL and a limit of quantification (LOQ) of 0.37 ng mL, requiring only 3 μL of EV-sample. This biosensor shows potential as a novel method for detecting and studying endothelial biomarkers associated with cardiovascular disease in EVs isolated from saliva, a capability not currently available with existing tools. Furthermore, it provides a key platform for expanding research to other biomarkers and diseases by monitoring protein cargos in the EVs, enhancing its utility across diverse clinical applications.

摘要

在本研究中,我们开发了一种生物传感器,该传感器使用经巯基十一烷酸(MUA)功能化的金丝网印刷电极(Au-SPE)和一种抗体,用于检测血管内皮钙黏蛋白(CD144),CD144是从唾液中分离的细胞外囊泡(EVs)上的一种内皮生物标志物蛋白。MUA功能化提供了一个稳定的平台来固定CD144抗体,确保对目标蛋白的检测。这种生物传感器将Au-SPE技术与免疫测定相结合,为检测EVs携带的CD144提供了一种快速、灵敏且非侵入性的方法。使用透射电子显微镜(TEM)和纳米颗粒跟踪分析(NTA)对唾液来源的EVs进行表征,证实了它们的形态和大小,其落在80-180 nm的预期范围内。NTA表明唾液-EVs中的颗粒浓度低于血清-EVs(对照),这突出了对这类EVs中EV货物进行灵敏检测的必要性。免疫检测证实唾液和血清来源的EVs中均存在CD144,血清中的浓度更高。通过显著的电阻变化证实了Au-SPEs用MUA和CD144抗体进行了功能化,并且使用原子力显微镜(AFM)来验证EV形态的保存及其免疫吸附后的捕获情况。校准曲线表明生物传感器原型对检测CD144阳性EVs具有高灵敏度,检测限(LOD)为0.111 ng/mL,定量限(LOQ)为0.37 ng/mL,仅需3 μL的EV样品。这种生物传感器作为一种检测和研究从唾液中分离的EVs中与心血管疾病相关的内皮生物标志物的新方法具有潜力,这是现有工具目前无法实现的能力。此外,它通过监测EVs中的蛋白质货物为将研究扩展到其他生物标志物和疾病提供了一个关键平台,增强了其在各种临床应用中的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8104/12012609/dd221a261184/d4ra08926j-f1.jpg

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