Squeezable Hydrogel Microparticles for Single Extracellular Vesicle Protein Profiling

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2024-10-29 DOI:10.1002/smll.202407809
Yoon Ho Roh, Renee-Tyler T. Morales, Emily Huynh, Uday Chintapula, David E. Reynolds, Renis J. Agosto-Nieves, Daniel Oh, Akari J. Seiner, Jianhua Lim, Christopher B. Rodell, Jina Ko
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引用次数: 0

Abstract

Extracellular vesicles (EVs) are promising for molecular diagnostics, but current analyses are limited by the rarity and compositional heterogeneity of EV protein expression. Therefore, single EV profiling methods require high sensitivity, multiplexing, and throughput to address these issues. Here a single EV analysis technique that utilizes squeezable methacrylated hyaluronic acid hydrogel microparticles (MHPs) is described as a scaffold to immobilize EVs and perform an integrated rolling circle amplification (RCA) assay for an ultra-sensitive and multiplex analysis of single EV proteins. EVs are prepared into MHPs in a high-throughput manner with droplet microfluidics and optimally labeled with antibody-oligonucleotide conjugates in MHPs without steric limitations. By designing MHPs with high compressibility, single EV protein signals are amplified as RCA products that can be aligned on the same plane by physically squeezing MHPs and visualized with low magnification. This method provides a simple and scalable single EV imaging analysis pipeline for identifying multiplex marker expression patterns from single EVs. For validation, the single EV heterogeneity of highly expressed cancer cell markers is profiled across different cancer cell lines. These findings exemplify squeezable MHPs as a robust platform with high sensitivity, multiplexing, and scalability for resolving single EV heterogeneity and advancing molecular assay technologies.

Abstract Image

用于单个细胞外囊泡蛋白质分析的可挤压水凝胶微颗粒
细胞外囊泡(EVs)有望用于分子诊断,但目前的分析受限于 EV 蛋白表达的稀有性和组成的异质性。因此,单个EV分析方法需要高灵敏度、复用性和通量来解决这些问题。本文介绍了一种利用可挤压的甲基丙烯酸透明质酸水凝胶微颗粒(MHPs)作为支架固定EV的单一EV分析技术,该技术可进行综合滚圆扩增(RCA)测定,从而对单一EV蛋白进行超灵敏的多重分析。利用液滴微流控技术,以高通量方式将EV制备到MHPs中,并在MHPs中用抗体-寡核苷酸共轭物进行最佳标记,而不受立体限制。通过设计具有高压缩性的 MHP,单个 EV 蛋白信号被放大为 RCA 产物,通过物理挤压 MHP,这些 RCA 产物可在同一平面上对齐,并以低放大率进行观察。这种方法提供了一个简单且可扩展的单个 EV 成像分析管道,用于识别单个 EV 的多重标记表达模式。为了进行验证,对不同癌细胞系中高表达癌细胞标记物的单个EV异质性进行了分析。这些研究结果证明,可挤压 MHPs 是一个强大的平台,具有高灵敏度、多重性和可扩展性,可用于解决单个 EV 的异质性并推动分子检测技术的发展。
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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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