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基于大小的细胞外囊泡分离:研究四跨膜蛋白与RNA之间的关系

Size-based separation of extracellular vesicles investigating the relationship between Tetraspanins and RNA.

作者信息

Yi Johan, Kim Suyeon, Lim Minyeob, Jeong Hwapyeong, Han Chungmin, Cho Siwoo, Park Jaesung

机构信息

Department of Mechanical Engineering, Pohang University of Science and Technology, 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeong-buk, 37673, Republic of Korea.

School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, 77 Cheongam-Ro, Nam-Gu, Pohang, Gyeong-buk, 37673, Republic of Korea.

出版信息

Anal Chim Acta. 2025 Jan 15;1335:343421. doi: 10.1016/j.aca.2024.343421. Epub 2024 Nov 14.

Abstract

BACKGROUND

Extracellular vesicles (EVs), nano-sized particles released by cells, exhibit inherent heterogeneity, posing challenges for precise classification. This study introduces a method utilizing the coffee ring effect for size-based separation analysis, driven by the outward flow during droplet evaporation with Marangoni flow resulting from a surface tension gradient.

RESULTS

The controlled separation of nanoparticles based on size was applied to characterize EV and virus-like particle (VLP) samples. Tetraspanin markers exhibited distinct distribution patterns in dried droplets, with CD63-single-positive particles being smaller than those positive for CD9, CD81, or gag. Additionally, using previously developed fluorescence nanoparticle tracking analysis and transmission electron microscopy, single vesicle analysis validated the size disparities in CD-positive particles. RNA analysis through the coffee ring effect and fluorescent NTA revealed differential patterns in EVs and VLPs, providing different insights into RNA packaging.

SIGNIFICANCE

This multifaceted approach enhances understanding EV heterogeneity, emphasizing the potential influence of cellular origin and biogenesis pathways on particle characteristics.

摘要

背景

细胞外囊泡(EVs)是细胞释放的纳米级颗粒,具有固有的异质性,这给精确分类带来了挑战。本研究介绍了一种利用咖啡环效应进行基于尺寸的分离分析的方法,该方法由液滴蒸发过程中的外向流动驱动,并伴有由表面张力梯度产生的马兰戈尼流。

结果

基于尺寸的纳米颗粒可控分离被应用于表征EV和病毒样颗粒(VLP)样品。四跨膜蛋白标记物在干燥液滴中呈现出不同的分布模式,CD63单阳性颗粒小于CD9、CD81或gag阳性的颗粒。此外,使用先前开发的荧光纳米颗粒跟踪分析和透射电子显微镜,单囊泡分析验证了CD阳性颗粒的尺寸差异。通过咖啡环效应和荧光纳米颗粒跟踪分析进行的RNA分析揭示了EV和VLP中的差异模式,为RNA包装提供了不同的见解。

意义

这种多方面的方法增强了对EV异质性的理解,强调了细胞起源和生物发生途径对颗粒特征的潜在影响。

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