Analyzing Extracellular Vesicle‐associated DNA Using Transmission Electron Microscopy at the Single EV‐level

Abstract Extracellular vesicles (EVs) play an important role in cell‐cell communication, carrying bioactive molecules including DNA. EV‐associated DNA (EV‐DNA) has created enormous interest in the field of biomarkers, particularly related to liquid biopsy. However, its analysis is challenging due to the nanoscale structure of EVs, the low abundance of EV‐DNA, and surrounding biogenetic debate. Therefore, novel protocols to enhance the accurate detection of EV‐DNA are essential to study its role in normal physiology and disease states. Here, we provide two protocols for confirming the presence of EV‐DNA from biological samples. In the first protocol, ultrathin sectioning of EVs is combined with immunogold labeling to detect the presence of double‐stranded (ds) DNA within the EV lumen using transmission electron microscopy (TEM). In the second protocol, whole‐mount EV immunogold labeling allows detailed morphological analysis of EVs and their surface‐associated DNA. Using TEM imaging, we have demonstrated that cancer‐cell‐derived individual EVs exhibit simultaneous positivity for dsDNA and the EV surface protein tetraspanin 9. We believe that this method can be used to label any proteins of interest inside as well as on the surface of EVs. This can aid in the characterization of single EVs and in the identification and verification of EV‐associated biomarkers. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1 : EV isolation from cell‐culture‐conditioned medium, EV embedding, ultrathin sectioning, labeling, and imaging Basic Protocol 2 : Whole‐mount immunolabeling of EV‐DNA