Figure 5
From: Functional roles of the membrane-associated AAV protein MAAP
Localization and intensity of MAAP and AAV-2 capsid proteins in transfected cells. (A) Representative confocal images of intracellular localisation of MAAP and capsid proteins at 24 hpt. Cells were co-transfected with wt-AAV2 and MAAP-S33-S39-S47 variant together with Ad helper plasmid, or with recombinant MAAP expression plasmid without Ad helper plasmid. The cells were immunolabelled with polyclonal antibody against MAAP (green) and monoclonal antibody against viral capsid proteins VP1, VP2 and VP3 (red). Blue corresponds to DAPI staining. Scale bars, 3 µm. For analyses, the cells were either mock transfected (n = 19), co-transfected with wt-AAV2 (n = 11), MAAP-S33-S39-S47 (n = 19), MAAP-W105 (n = 20), MAAP-L106 (n = 17), MAAP-L110 (n = 20) together with Ad helper plasmid, or transfected with the recombinant MAAP plasmid (n = 18). (B) Quantitative analyses of the total intensities of MAAP (light grey) and capsid proteins (dark grey) at 24 hpt. (C) Quantitative analyses of the relative intensity of nuclear (dark grey) in comparison to cytoplasmic capsid proteins (light grey) at 24 hpt. For analysis, the cells were immunolabelled with antibodies against viral capsid protein VP1, VP2 and VP3 (red) and the nuclear boundary segmentation was based on distribution of DAPI-labelled chromatin (blue). The error bars show the SEM.
