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. 2009 May 1;284(18):12000–12007. doi: 10.1074/jbc.M808028200

FIGURE 3.

FIGURE 3.

Localization of QD-CaM probe to the outer surface of the plasma membrane of both lily pollen and tobacco BY-2 protoplasts. AE, transmission electron micrographs of lily pollen protoplasts incubated with QD-CaM probe or unbound QDs. A, low magnification image of a protoplast incubated with QD-CaM probe. B, higher magnification of area highlighted in A. Note that the QD-CaM probe was confined to the outer surface of the protoplast. C, higher magnification of the area highlighted in B. Arrowheads identify single QD-CaM probes bound to the outer surface of the plasma membrane. D and E, lily protoplast incubated with unbound QDs and QD-CaM TR1C probe, respectively. No particles were detected bound to the plasma membrane. F, presence of QD-CaM probe bound to the plasma membrane of a BY-2 protoplast. G, higher magnification of the area highlighted in F. Arrowheads identify single QD-CaM probes bound to the outer surface of the plasma membrane. H, BY-2 protoplast incubated with QD-CaM TR1C probe; no particles were bound to the plasma membrane. Scale bars, A, 10 μm; BH, 0.5 μm. M, mitochondria; L, lipid.