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用于单细胞外囊泡蛋白质谱分析的可挤压水凝胶微粒

Squeezable Hydrogel Microparticles for Single Extracellular Vesicle Protein Profiling.

作者信息

Roh Yoon Ho, Morales Renee-Tyler T, Huynh Emily, Chintapula Uday, Reynolds David E, Agosto-Nieves Renis J, Oh Daniel, Seiner Akari J, Lim Jianhua, Rodell Christopher B, Ko Jina

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.

Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, 19104, USA.

出版信息

Small. 2025 Jan;21(1):e2407809. doi: 10.1002/smll.202407809. Epub 2024 Oct 29.

DOI:10.1002/smll.202407809
PMID:39468876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11707585/
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.

摘要

细胞外囊泡(EVs)在分子诊断方面具有广阔前景,但目前的分析受到EV蛋白表达的稀有性和组成异质性的限制。因此,单个EV分析方法需要高灵敏度、多重分析能力和高通量来解决这些问题。本文描述了一种利用可挤压的甲基丙烯酸化透明质酸水凝胶微粒(MHP)的单个EV分析技术,作为固定EVs的支架,并进行集成滚环扩增(RCA)分析,以实现对单个EV蛋白的超灵敏和多重分析。通过液滴微流控技术以高通量方式将EVs制备成MHP,并在没有空间位阻限制的情况下在MHP中用抗体 - 寡核苷酸缀合物进行最佳标记。通过设计具有高压缩性的MHP,单个EV蛋白信号作为RCA产物被放大,这些产物可以通过物理挤压MHP在同一平面上排列,并以低倍放大倍数进行可视化。该方法提供了一个简单且可扩展的单个EV成像分析流程,用于从单个EVs中识别多重标记表达模式。为了进行验证,对不同癌细胞系中高表达的癌细胞标记物的单个EV异质性进行了分析。这些发现证明了可挤压的MHP是一个强大的平台,具有高灵敏度、多重分析能力和可扩展性,可用于解决单个EV异质性并推动分子检测技术的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/5bdda742a04c/SMLL-21-2407809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/3364ae743f9a/SMLL-21-2407809-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/68b8ea3bea5e/SMLL-21-2407809-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/4111f4d2a664/SMLL-21-2407809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/bf13826116bf/SMLL-21-2407809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/5bdda742a04c/SMLL-21-2407809-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/3364ae743f9a/SMLL-21-2407809-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/68b8ea3bea5e/SMLL-21-2407809-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/4111f4d2a664/SMLL-21-2407809-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/bf13826116bf/SMLL-21-2407809-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fb9/11707585/5bdda742a04c/SMLL-21-2407809-g002.jpg

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