膜
脂质体
小泡
离子霉素
化学
生物物理学
微流控
纳米技术
生物化学
生物
材料科学
细胞内
作者
Krzysztof M. Bąk,Daniel Edwards,Dylan B. George,Bhanu Singh,Ryan Ferguson,Tianxiao Zhao,Kristin Piché,Ariel Louwrier,Scott L. Cockroft,Mathew H. Horrocks
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-04-07
卷期号:64 (26): e202503678-e202503678
被引量:2
标识
DOI:10.1002/anie.202503678
摘要
Abstract Cell membrane disruption is associated with numerous diseases and underlies the activity of various antimicrobial agents. The rapid screening of compounds capable of disrupting or permeabilizing biological membranes is essential to the search for new therapeutic drugs. Here, we present a single‐molecule confocal microscopy assay integrated with fast‐flow microfluidics to study membrane permeabilization in large unilamellar vesicles (LUVs) containing as few as seven dye molecules. This assay eliminates the need for liposome immobilization and achieves detection rates in the range of 1000 vesicles per minute, offering unparalleled sensitivity and detection limits as low as 135 pM, corresponding to just eight permeabilizing molecules per vesicle for active compounds such as ionomycin. It provides a robust platform for investigating membrane‐disrupting agents, including those with antimicrobial properties or implicated in neurodegenerative diseases.
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