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. 2011 Oct 14;6(10):e26206. doi: 10.1371/journal.pone.0026206

Figure 2. Comparison of the subcellular localization of wild type Endoglin with two (L32R and C53R) orphan domain HHT1-causing mutants.

Figure 2

HeLa cells were transiently transfected with the C-terminally HA-tagged Endoglin pCMV5 plasmids (panels A-C, G-I and M-O) or co-transfected with the same plasmids and the EGFP-tagged H-Ras plasmid (Panels D–F, J–L and P–R) and processed for fluorescence confocal microscopy as described in the methods. The HA tagged proteins were detected with Anti-HA monoclonal antibodies (red panels A, D, G, J. M and P) and the ER marker calnexin was detected with anti-calnexin polyclonal antibodies (panels B, H and N). GFP-H-Ras staining is shown in panels E, K and Q. The wild type predominantly showed plasma membrane localization as evidenced by its co-localization with Ras (D–F). On the other hand the two mutants (L32R and C53R) showed ER localization (G–R).