| Literature DB >> 32815321 |
Jouha Min1, Taehwang Son1, Jae-Sang Hong1, Pike See Cheah2,3, Andreas Wegemann1,4, Koushik Murlidharan5, Ralph Weissleder1,6,7, Hakho Lee1,6, Hyungsoon Im1,6.
Abstract
Extracellular vesicles (EVs)-nanoscale phospholipid vesicles secreted by cells-present new opportunities for molecular diagnosis from non-invasive liquid biopsies. Single EV protein analysis can be extremely valuable in studying EVs as circulating cancer biomarkers, but it is technically challenging due to weak detection signals associated with limited amounts of epitopes and small surface areas for antibody labeling. Here, a new, simple method that enables multiplexed analyses of EV markers with improved sensitivities is reported. Specifically, plasmon-enhanced fluorescence detection is implemented that amplifies fluorescence signals using surface plasmon resonances excited by periodic gold nanohole structures. It is shown that fluorescence signals in multiple channels are amplified by one order of magnitude, and both transmembrane and intravesicular markers can be detected at the single EV level. This approach can offer additional insight into understanding subtypes, heterogeneity, and production dynamics of EVs during disease development and progression.Entities:
Keywords: biosensing; cancer; extracellular vesicles; nanoholes; plasmon-enhanced fluorescence
Year: 2020 PMID: 32815321 PMCID: PMC7718316 DOI: 10.1002/adbi.202000003
Source DB: PubMed Journal: Adv Biosyst ISSN: 2366-7478