生物正交化学
肽
化学
小泡
细胞外小泡
化学生物学
生物物理学
脂质双层
生物化学
膜
细胞内
细胞外
微泡
细胞生物学
核酸
外体
双层
纳米技术
肽核酸
膜生物学
生物物理化学
靶肽
脂泡
胞外囊泡
合成生物学
人工细胞
底物特异性
出处
期刊:Biochemistry
[American Chemical Society]
日期:2026-01-13
卷期号:65 (5): 505-516
标识
DOI:10.1021/acs.biochem.5c00700
摘要
Extracellular vesicles (EVs) are nanosized lipid bilayer vesicles released by all cells. EVs carry nucleic acids, proteins, lipids, and metabolites in intercellular communication. As potential liquid-biopsy biomarkers and drug-delivery vehicles for diseases, however, isolating specific EV subpopulations remains challenging owing to their high heterogeneity in size, density, and surface protein markers. We utilized chemical biology tools to develop EV membrane-curvature probes, including MARCKS-ED and other peptides. These short, membrane-anchoring peptides detect the fluid membrane of EVs and report membrane curvature. Here, we review the peptide selection principles, bioorthogonal reaction engineering mechanisms, and applications of these EV peptide probes and discuss future directions, such as stimulus-responsive or artificial intelligence-assisted peptide probe design for on-demand EV capture and subpopulation.
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