Xu Kun, Jin Yulong, Li Yongming, Huang Yanyan, Zhao Rui
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Analytical Chemistry for Living Biosystems, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
School of Chemistry, University of Chinese Academy of Sciences, Beijing, China.
Front Chem. 2022 Feb 24;10:844124. doi: 10.3389/fchem.2022.844124. eCollection 2022.
Exosomes are membrane extracellular vesicles secreted by almost all kinds of cells, which are rich in proteins, lipids, and nucleic acids. As a medium of intercellular communication, exosomes play important roles in biological processes and are closely related to the occurrence, and development of many diseases. The isolation of exosomes and downstream analyses can provide important information to the accurate diagnosis and treatment of diseases. However, exosomes are various in a size range from 30 to 200 nm and exist in complex bio-systems, which provide significant challenges for the isolation and enrichment of exosomes. Different methods have been developed to isolate exosomes, such as the "gold-standard" ultracentrifugation, size-exclusion chromatography, and polymer precipitation. In order to improve the selectivity of isolation, affinity capture strategies based on molecular recognition are becoming attractive. In this review, we introduced the main strategies for exosome isolation and enrichment, and compared their strengths and limitations. Furthermore, combined with the excellent performance of targeted peptides, we summarized the application of peptide recognition in exosome isolation and engineering modification.
外泌体是几乎所有类型细胞分泌的膜性细胞外囊泡,富含蛋白质、脂质和核酸。作为细胞间通讯的一种介质,外泌体在生物学过程中发挥重要作用,并且与许多疾病的发生和发展密切相关。外泌体的分离及下游分析可为疾病的准确诊断和治疗提供重要信息。然而,外泌体大小在30到200纳米之间,且存在于复杂的生物系统中,这为外泌体的分离和富集带来了巨大挑战。目前已开发出不同的方法来分离外泌体,如“金标准”超速离心法、尺寸排阻色谱法和聚合物沉淀法。为了提高分离的选择性,基于分子识别的亲和捕获策略正变得具有吸引力。在本综述中,我们介绍了外泌体分离和富集的主要策略,并比较了它们的优缺点。此外,结合靶向肽的优异性能,我们总结了肽识别在外泌体分离和工程修饰中的应用。