Publication:
Multiplex Biomarker Screening Assay for Urinary Extracellular Vesicles Study: A Targeted Label-Free Proteomic Approach

dc.contributor.authorSomchai Chutipongtanateen_US
dc.contributor.authorKenneth D. Greisen_US
dc.contributor.otherUniversity of Cincinnati College of Medicineen_US
dc.contributor.otherFaculty of Medicine, Ramathibodi Hospital, Mahidol Universityen_US
dc.date.accessioned2019-08-28T07:10:59Z
dc.date.available2019-08-28T07:10:59Z
dc.date.issued2018-12-01en_US
dc.description.abstract© 2018, The Author(s). The recent advance in targeted label-free proteomics, SWATH-MS, can provide consistent protein detection and reproducible protein quantitation, which is a considerable advantage for biomarker study of urinary extracellular vesicles. We developed a SWATH-MS workflow with a curated spectral library of 1,145 targets. Application of the workflow across nine replicates of three sample types (exosome-like vesicles (ELVs), microvesicles (MVs) and urine proteins (UPs)) resulted in the quantitation of 888 proteins at FDR <1%. The median-coefficient of variation of the 888 proteins in the ELV sample was 7.7%, indicating excellent reproducibility. Data analysis showed common exosome markers, (i.e. CD9, CD63, ALIX, TSG101 and HSP70) were enriched in urinary ELVs as compared to MVs and UPs. The use of a multiplex biomarker screening assay focused on ELVs was investigated, and perspectives in future applications are discussed.en_US
dc.identifier.citationScientific Reports. Vol.8, No.1 (2018)en_US
dc.identifier.doi10.1038/s41598-018-33280-7en_US
dc.identifier.issn20452322en_US
dc.identifier.other2-s2.0-85054772012en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/47475
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054772012&origin=inwarden_US
dc.subjectMultidisciplinaryen_US
dc.titleMultiplex Biomarker Screening Assay for Urinary Extracellular Vesicles Study: A Targeted Label-Free Proteomic Approachen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054772012&origin=inwarden_US

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