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Antibody-Based Assays for Phenotyping of Extracellular Vesicles

Authors :
Malene Jørgensen
Lotte Hatting Pugholm
Anne Louise Revenfeld
Evo Kristina Lindersson Søndergaard
Source :
BioMed Research International, Pugholm, L H, Revenfeld, A L, Søndergaard, E K L & Jørgensen, M M 2015, ' Antibody-Based Assays for Phenotyping of Extracellular Vesicles ', BioMed Research International, vol. 2015, 524817 . https://doi.org/10.1155/2015/524817, Pugholm, L H, Revenfeld, A L S, Søndergaard, E K L & Jørgensen, M M 2015, ' Antibody-based assays for phenotyping of extracellular vesicles ', BioMed Research International, vol. 2015, 524817 . https://doi.org/10.1155/2015/524817, BioMed Research International, Vol 2015 (2015)
Publication Year :
2015
Publisher :
Hindawi Publishing Corporation, 2015.

Abstract

Extracellular vesicles (EVs) are a heterogeneous population of membrane-enclosed vesicles. EVs are recognized as important players in cell-to-cell communication and are described to be involved in numerous biological and pathological processes. The fact that EVs are involved in the development and progression of several diseases has formed the basis for the use of EV analysis in a clinical setting. As the interest in EVs has increased immensely, multiple techniques have been developed aiming at characterizing these vesicles. These techniques characterize different features of EVs, like the size distribution, enumeration, protein composition, and the intravesicular cargo (e.g., RNA). This review focuses on techniques that exploit the specificity and sensitivity associated with antibody-based assays to characterize the protein phenotype of EVs. The protein phenotype of EVs can provide information on the functionality of the vesicles and may be used for identification of disease-related biomarkers. Thus, protein profiling of EVs holds great diagnostic and prognostic potential.

Details

Language :
English
ISSN :
23146141 and 23146133
Volume :
2015
Database :
OpenAIRE
Journal :
BioMed Research International
Accession number :
edsair.doi.dedup.....e62e5b1cee6ed0b800a3f69a7fa35290
Full Text :
https://doi.org/10.1155/2015/524817