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Encyclopedia of Experiments: Immunology

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An Immunofluorescence Method to Measure the Neutralization of Human Cytomegalovirus

 

An Immunofluorescence Method to Measure the Neutralization of Human Cytomegalovirus

Article

Transcript

Take serial dilutions of antibodies specific for human cytomegalovirus, or HCMV.

Upon adding HCMV, the antibodies bind to glycoprotein B on the viral envelope, neutralizing the virus.

Transfer the mixture onto human fibroblasts and incubate.

A trimer glycoprotein complex on the non-neutralized viruses binds to specific cellular receptors, triggering glycoprotein B-mediated virus-host membrane fusion and releasing the genomic DNA-containing nucleocapsid inside.

The released genome enters the nucleus, encoding nuclear-localized immediately early, or IE, proteins.

Antibody-neutralization prevents viral entry into the cells.

Remove the non-internalized viruses. Treat with ethanol at a sub-zero temperature to fix and permeabilize the cells.

Introduce a primary antibody that binds to the IE proteins.

Add a fluorophore-conjugated secondary antibody that binds to the primary antibody and a fluorescent stain that binds to DNA.

Under a microscope, detect dual-stained cells that are virus-infected. Calculate the percentage of infected cells to determine virus neutralization at the different antibody concentrations.

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