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Resolution: standard / high Figure 7.
Subcellular localization of the endoplasmic reticulum-targeted green fluorescent protein-elastin-like
polypeptide fusion protein (pPGEK) in Nicotiana benthamiana leaves. (A) Electron microscopy confirmed the location of numerous newly-formed endoplasmic reticulum-
(ER-)derived protein bodies (PBs) (examples indicated by asterisks) in the cytoplasm
of the leaf cells. (B-D) Progressively higher magnifications of the PBs seen in (A). (B) The novel PBs occupied
the cytosolic space between the tonoplast (indicated by an arrowhead) and the plasma
membrane (indicated by an arrow). (C) The PBs were clearly surrounded by a membrane
that appears to no longer be contiguous with the ER. (D) The PB membrane was decorated
with ribosomes (indicated with arrows), strongly suggesting that the PBs were originally
derived from the rough ER. (E, F) Immunogold localization confirmed the presence of green fluorescent protein-elastin-like
polypeptide (GFP-ELP) inside the novel cytoplasmic PBs in ultrathin sections of N. benthamiana leaves using anti-ELP (E) and anti-GFP (F) antibodies detected with goat anti-rabbit
or anti-mouse IgG conjugated to 15 nm gold particles. No significant immunolabeling
was observed in other subcellular compartments or wild-type plants. The different
subcellular compartments were labeled: Cp, chloroplast; CW, cell wall; Mt, mitochondria;
LB, lipid body; LV, lytic vacuole; *, induced protein body. Bar, 2 μm (A); 500 nm
(B, C, E, F); 100 nm (D).
Conley et al. BMC Biology 2009 7:48 doi:10.1186/1741-7007-7-48 |