Automated Enrichment and Coextraction Pipeline for Efficient Analysis of Urinary Extracellular Vesicle Protein and RNA.
1/5 보강
Extracellular vesicle (EV) cargoes have great potential as promising biomarkers for disease diagnosis.
APA
Liu Y, Zhang G, et al. (2025). Automated Enrichment and Coextraction Pipeline for Efficient Analysis of Urinary Extracellular Vesicle Protein and RNA.. Journal of proteome research, 24(7), 3689-3696. https://doi.org/10.1021/acs.jproteome.5c00357
MLA
Liu Y, et al.. "Automated Enrichment and Coextraction Pipeline for Efficient Analysis of Urinary Extracellular Vesicle Protein and RNA.." Journal of proteome research, vol. 24, no. 7, 2025, pp. 3689-3696.
PMID
40545677 ↗
Abstract 한글 요약
Extracellular vesicle (EV) cargoes have great potential as promising biomarkers for disease diagnosis. However, traditional methods for EV enrichment and cargo extraction are inefficient, limiting the accessibility of valuable biological information. Here, we present a bead-based pipeline designed to efficiently enrich EVs from urine while simultaneously extracting both EV protein and RNA. Compared to traditional methods involving ultracentrifugation (UC) for EV isolation, acetone precipitation for protein extraction, and TRIzol for RNA extraction, the new pipeline achieved over a 5-fold improvement in EV protein and RNA yield. Additionally, it reduced the duration from approximately 2 days to just 1 h. When applied to the noninvasive diagnosis of prostate cancer (PCa), the pipeline demonstrated excellent diagnostic performance, with a panel of EV protein and RNA markers achieving an AUC of 0.82. This efficient and streamlined pipeline provides a robust tool for comprehensive EV cargo analysis and holds great potential for advancing noninvasive diagnostics in clinical settings.
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