| Literature DB >> 33159572 |
Meng Li1,2,3, Doudou Lou2, Joyce Chen4, Keqing Shi5, Yong Wang3, Qingfu Zhu2, Fei Liu6,7, Yating Zhang8.
Abstract
Salivary extracellular vesicles (EVs), as novel functional carriers and potential biomarkers, are usually obtained by ultracentrifugation (UC) and polyethylene glycol (PEG)-based precipitation methods. However, salivary EVs obtained by these two methods have not been systematically compared. Here, we perform an in-depth analysis on EVs isolated by these two methods using proteomics. Both methods obtain EVs ranging from 40 to 210 nm, with the PEG method resulting in a wider size distribution. PEG-separated products were irregularly shaped and aggregated, while UC-separated ones were monodispersed and teacup-shaped. Additionally, the expression of EV-specific markers was higher in UC-separated EVs. Using tandem mass spectrometry proteomics, we identified and quantified 1217 kinds of saliva exosomal proteins and 361 kinds of differential proteins, showing that UC can isolate more EV-related proteins. These results offer some guidance for EV separating and provide potential direction for the use of EVs in non-invasive diagnosis.Entities:
Keywords: Extracellular vesicles; Polymer-based precipitation; Proteomics; Saliva; Ultracentrifugation
Year: 2020 PMID: 33159572 DOI: 10.1007/s00216-020-03004-w
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.142