Immunocapture and Flow Cytometry of Extracellular Vesicles for Antigenic Characterization
내레이션 대본
Begin by combining 60 microliters of MNPs per condition and 5 microliters of labeled Fab fragments specific for the isotype of the capture antibody of interest in a 1.5-milliliter microcentrifuge tube. Incubate the solution at room temperature for 30 minutes with continuous mixing. Then, pre-wet a 100k concentrator with 300 microliters of PBS, and spin the concentrator in a microcentrifuge.
At the end of centrifugation, purify the labeled complexes on a 100k column, followed by another centrifugation, resuspending the pellet in 200 microliters of fresh PBS. To capture the particles of interest, incubate the antibody-labeled MNPs with the particle of interest for the appropriate incubation period and temperature.
Next, block any non-specific FC binding with the appropriate species of IgG antibody, gently vortex, and incubate the particle solution for 3 to 5 minutes at room temperature. Then, add the manufacturer-recommended concentration of each detection antibody to the particles or isotype control antibodies to the isotype control sample for an additional 20 minutes incubation at room temperature.
To separate the MNP-captured particles from the unbound antibody, first, place a magnetic separation column in a separator magnet and pre-wet the column with 500 microliters of wash buffer. Allow the wash buffer to flow through the column. Then, add the MNP particle complexes to the column, collecting the flowthrough in a waste container.
When all of the complex solution has passed through the column, wash the column three times with 500 microliters of wash buffer. Then, transfer the column to a 12-by-75 millimeter tube. After three minutes, add 200 microliters of PBS, allowing the beads to elute by gravity.
When all of the PBS has passed through the column, add 200 microliters of fresh PBS to the tube, and fix the particles with 200 microliters of 4% paraformaldehyde. Next, load 0.22-micron-filtered PBS onto a flow cytometer and adjust the PMT voltage on the cytometer until the filtered PBS shows zero to very few events. Then, run the MNP-captured particles using a low flow with a 0.04-micron in-line filter for sheath fluid placed in series behind the standard 0.2-micron sheath filter to further eliminate any false events.
