Sectioning, Staining and TEM Imaging of Embedded Exosomes: A Protocol To Visualize the Structural Features of Exosomes Using TEM
DEŞİFRE METNİ
Exosomes are nanosized, spherical vesicles enclosed by a lipid bilayer containing DNA, RNA, and protein molecules present inside the lumen.
To visualize the exosome structure using transmission electron microscopy, or TEM, begin by taking an exosome block – a solid matrix block containing the embedded exosomes. Using an ultra-microtome, obtain ultrathin sections of the exosome block.
Collect the exosome section on a suitable grid and allow it to adhere to the surface. The grid provides stable support to the exosome specimen for subsequent staining steps.
Next, position the grid over a drop of uranyl acetate – a heavy metal stain – and incubate for the desired duration. Uranyl ions interact with lipids, proteins, DNAs, and RNAs present in the exosomes.
Subsequently, stain the exosome section with lead citrate, which also binds to the exosomal biomolecules. Lead citrate weakly binds to the pre-bound uranyl ions and enhances the contrast against background during imaging.
Observe the doubly stained exosomes using TEM. TEM focuses the electron beam on the exosome sample. Stained regions in the exosome scatter electrons more strongly in comparison to the unstained regions.
The objective aperture filters these highly scattered electrons. Thus, exosomes containing stained biomolecules appear darker than the background.
