Peptide-Engineered Biomimetic Nanoplatform with Cell-Membrane Camouflage Streamlines High-Performance Isolation and Quantitation of Extracellular Vesicles

IF 9.1 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Zichen Huang, Zhikai Fang, Kai Ni, Ziyi Zhang, Zhan Zhang, Yihua Bei*, Zhaoyin Wang*, Ya Cao* and Jing Zhao*, 
{"title":"Peptide-Engineered Biomimetic Nanoplatform with Cell-Membrane Camouflage Streamlines High-Performance Isolation and Quantitation of Extracellular Vesicles","authors":"Zichen Huang,&nbsp;Zhikai Fang,&nbsp;Kai Ni,&nbsp;Ziyi Zhang,&nbsp;Zhan Zhang,&nbsp;Yihua Bei*,&nbsp;Zhaoyin Wang*,&nbsp;Ya Cao* and Jing Zhao*,&nbsp;","doi":"10.1021/acssensors.5c00827","DOIUrl":null,"url":null,"abstract":"<p >Reliable isolation and quantitation of extracellular vesicles (EVs), which function as natural bioactive nanocarriers in biological processes, are essential to uncovering their underlying mechanisms and applications. To meet these requirements, we present here a peptide-engineered biomimetic nanoplatform featuring cell-membrane camouflage. This biomimetic nanoplatform utilizes specific peptide ligands to facilitate the “capture–release” isolation of EVs while enhancing performance by harnessing the antifouling and fluidity advantages afforded by the camouflage of red blood cell membranes. Furthermore, this nanoplatform streamlines the electrochemical quantitation of EVs via a nondestructive labeling and delabeling process, showing accuracy comparable to that of widely used nanoparticle tracking analysis. Validating with EVs from breast cancer cells and human embryonic stem cells, this nanoplatform is also proved to effectively maintain the biological activities of the isolated EVs, thereby enabling precise regulation of cell migration and antiapoptotic response. As such, this biomimetic nanoplatform stands as a highly effective solution for isolating and quantitatively assessing EVs from diverse sources, thus propelling the potential applications of EVs in biomedical and clinical research.</p>","PeriodicalId":24,"journal":{"name":"ACS Sensors","volume":"10 8","pages":"5704–5713"},"PeriodicalIF":9.1000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Sensors","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acssensors.5c00827","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Reliable isolation and quantitation of extracellular vesicles (EVs), which function as natural bioactive nanocarriers in biological processes, are essential to uncovering their underlying mechanisms and applications. To meet these requirements, we present here a peptide-engineered biomimetic nanoplatform featuring cell-membrane camouflage. This biomimetic nanoplatform utilizes specific peptide ligands to facilitate the “capture–release” isolation of EVs while enhancing performance by harnessing the antifouling and fluidity advantages afforded by the camouflage of red blood cell membranes. Furthermore, this nanoplatform streamlines the electrochemical quantitation of EVs via a nondestructive labeling and delabeling process, showing accuracy comparable to that of widely used nanoparticle tracking analysis. Validating with EVs from breast cancer cells and human embryonic stem cells, this nanoplatform is also proved to effectively maintain the biological activities of the isolated EVs, thereby enabling precise regulation of cell migration and antiapoptotic response. As such, this biomimetic nanoplatform stands as a highly effective solution for isolating and quantitatively assessing EVs from diverse sources, thus propelling the potential applications of EVs in biomedical and clinical research.

Abstract Image

具有细胞膜伪装的多肽工程仿生纳米平台简化了细胞外囊泡的高效分离和定量。
细胞外囊泡(EVs)作为生物过程中的天然生物活性纳米载体,其可靠的分离和定量对揭示其潜在机制和应用至关重要。为了满足这些要求,我们提出了一种具有细胞膜伪装功能的肽工程仿生纳米平台。这种仿生纳米平台利用特定的肽配体来促进电动汽车的“捕获-释放”隔离,同时利用红细胞膜伪装提供的防污和流动性优势提高性能。此外,该纳米平台通过非破坏性标记和去标记过程简化了电动汽车的电化学定量,显示出与广泛使用的纳米颗粒跟踪分析相当的准确性。通过对乳腺癌细胞和人胚胎干细胞的验证,该纳米平台也被证明可以有效地维持分离的ev的生物活性,从而能够精确调节细胞迁移和抗凋亡反应。因此,这种仿生纳米平台是分离和定量评估来自不同来源的电动汽车的高效解决方案,从而推动电动汽车在生物医学和临床研究中的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ACS Sensors
ACS Sensors Chemical Engineering-Bioengineering
CiteScore
14.50
自引率
3.40%
发文量
372
期刊介绍: ACS Sensors is a peer-reviewed research journal that focuses on the dissemination of new and original knowledge in the field of sensor science, particularly those that selectively sense chemical or biological species or processes. The journal covers a broad range of topics, including but not limited to biosensors, chemical sensors, gas sensors, intracellular sensors, single molecule sensors, cell chips, and microfluidic devices. It aims to publish articles that address conceptual advances in sensing technology applicable to various types of analytes or application papers that report on the use of existing sensing concepts in new ways or for new analytes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信