Human immunodeficiency virus (HIV) infects cells that have both CD4 and CCR5 cell surface
molecules. The viral nucleic acid molecules are enclosed in a protein capsid, and the protein capsid is
itself contained inside an envelope consisting of a lipid bilayer membrane and viral glycoproteins. One
hypothesis for viral entry into cells is that binding of HIV membrane glycoproteins to CD4 and CCR5
initiates fusion of the HIV membrane with the plasma membrane, releasing the viral capsid into the
cytoplasm. An alternative hypothesis is that HIV gains entry into the cell via receptor-mediated
endocytosis, and membrane fusion occurs in the endocytotic vesicle. To test these alternative hypotheses
for HIV entry, researchers labeled the lipids on the HIV membrane with a red fluorescent dye.
66) What would be observed by live-cell fluorescence microscopy if the red fluorescent lipid dye-
labeled HIV membrane fuses with the target cell plasma membrane?
A) A spot of red fluorescence will remain on the infected cell’s plasma membrane, marking the site of
membrane fusion and HIV entry.
B) The red fluorescent dye-labeled lipids will diffuse in the infected cell’s plasma membrane and
become difficult to detect.
C) A spot of red fluorescence will move into the infected cell’s cytoplasm.
D) A spot of red fluorescence will remain outside the cell after delivering the viral capsid.
E) Fluorescence microscopy does not have enough resolution to visualize fluorescently labeled HIV
virus particles.
67) What would be observed by live-cell fluorescence microscopy if HIV is endocytosed first, and then
fuses with the endocytotic vesicle membrane?
A) A spot of red fluorescence will remain on the infected cell’s plasma membrane, marking the site of
membrane fusion and HIV entry.
B) The red fluorescent dye-labeled lipids will diffuse in the endocytotic vesicle membrane and become
difficult to detect.
C) A spot of red fluorescence will move into the infected cell’s interior.
D) A spot of red fluorescence will remain outside the cell after delivering the viral capsid.
E) Fluorescence microscopy does not have enough resolution to visualize fluorescently labeled HIV
virus particles.