Translocation of Endothelial Nitric-Oxide Synthase Involves a Ternary Complex with Caveolin-1 and NOSTRIN
Mol. Biol. Cell Schilling et al.
17: 3870
Supplemental Material
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Figure 1
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Co-immunoprecipitations from CHO-eNOS cells infected with SFV-HA-NOSTRIN242-506 using anti-eNOS. Caveolin-1 peptides cav82-101 (scaffolding domain), cav61-81 or unrelated peptide (RLC24) were added to the lysates as indicated. Immunoblots were probed for NOSTRIN (anti-HA) and eNOS.
Figure 2
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Caveolin-1 and eNOS accumulate in the perinuclear region of cells co-expressing eNOS, NOSTRIN and mutant dynamin. CHO-eNOS cells were transfected with dynamin-K44A-GFP (dyn-K44A) in the absence (E-H) or presence of co-transfected NOSTRIN (A-D, I-L). (A-D) NOSTRIN and dyn-K44A co-localize. (E-H) Expression of dyn-K44A alone does not alter localization of caveolin or eNOS, except for a slight change in Golgi morphology. (I-L) eNOS and caveolin appear to be stuck in the perinuclear region in cells expressing NOSTRIN and dyn-K44A. Bars 10 μm.