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Calibration-free analysis of surface proteins on single extracellular vesicles enabled by DNA nanostructure.
Guo, Kaizhu; Li, Zongbo; Win, Allison; Coreas, Roxana; Adkins, Gary Brent; Cui, Xinping; Yan, Dong; Cao, Minghui; Wang, Shizhen Emily; Zhong, Wenwan.
Afiliación
  • Guo K; Department of Chemistry, University of California-Riverside, Riverside, CA, 92521, USA.
  • Li Z; Department of Chemistry, University of California-Riverside, Riverside, CA, 92521, USA.
  • Win A; Department of Chemistry, University of California-Riverside, Riverside, CA, 92521, USA.
  • Coreas R; Environmental Toxicology Graduate Program, University of California-Riverside, Riverside, CA, 92521, USA.
  • Adkins GB; Department of Chemistry, University of California-Riverside, Riverside, CA, 92521, USA.
  • Cui X; Department of Statistics, University of California-Riverside, Riverside, CA, 92521, USA.
  • Yan D; Nanofabrication Facility, University of California-Riverside, Riverside, CA, 92521, USA.
  • Cao M; Department of Pathology, University of California San Diego, La Jolla, CA, 92093, USA.
  • Wang SE; Department of Pathology, University of California San Diego, La Jolla, CA, 92093, USA.
  • Zhong W; Department of Chemistry, University of California-Riverside, Riverside, CA, 92521, USA; Environmental Toxicology Graduate Program, University of California-Riverside, Riverside, CA, 92521, USA. Electronic address: wenwan.zhong@ucr.edu.
Biosens Bioelectron ; 192: 113502, 2021 Nov 15.
Article en En | MEDLINE | ID: mdl-34298496
Extracellular vesicles (EVs) are essential intercellular communicators that are of increasing interest as diagnostic biomarkers. Exploring their biological functions and clinical values, however, remains challenging due to their small sizes and high heterogeneity. Herein, we report an ultrasensitive method that employs target-initiated construction of DNA nanostructure to detect single EVs with an input as low as 100 vesicles/µL. Taking advantage of both DNA nanostructure labeling and EV membrane staining, the method can also permit calibration-free analysis of the protein profiles among different EV samples, leading to clear EV differentiation by their cell of origin. Moreover, this method allows co-localization of dual protein markers on the same EV, and the increased number of EVs carrying dual tumor proteins present in human serum could differentiate cancer patients at the early developmental stage from healthy controls. Our results demonstrate the great potential of this single-EV visualization method in non-invasive detection of the EV-based protein biomarkers for cancer diagnosis and treatment monitoring.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Técnicas Biosensibles / Nanoestructuras / Vesículas Extracelulares Límite: Humans Idioma: En Revista: Biosens bioelectron Asunto de la revista: BIOTECNOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Técnicas Biosensibles / Nanoestructuras / Vesículas Extracelulares Límite: Humans Idioma: En Revista: Biosens bioelectron Asunto de la revista: BIOTECNOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos