In Situ Localization and in Vitro Induction of Plant COPI-Coated Vesicles

Immunogold Labeling of Cryosections with Plant COP Antibodies I.

Shown is the distribution of Atγ-COP homolog in maize roots.

(A) and (B) Golgi stacks from cells near the meristem.

(C) Golgi stack from a root cap cell.

Arrowheads point to labeled budding and released COPI-coated vesicles. c, cis-face of a Golgi stack; t, trans-face of a Golgi stack; SV, slime-containing secretory vesicle. Bars = 100 nm.

Immunogold Labeling of Cryosections with Plant COP Antibodies II.

Shown is labeling of maize root Golgi stacks from cells near the meristem.

(A) and (B) Labeling with Zm∂- and Zmε-COP antibodies, respectively.

(C) Labeling with AtArf1p antibodies.

Arrows point to clathrin-coated vesicles; arrowheads indicate budding COPI-coated vesicles. c, cis-face of a Golgi stack; t, trans-face of a Golgi stack. Bars = 100 nm.

Immunogold Labeling of Cryosections with Plant COP Antibodies III.

Shown is labeling of Arabidopsis root Golgi stacks.

(A) Labeling with Atγ-COP antibodies.

(B) Labeling with Zm∂-COP antibodies.

(C) Labeling with Zmε-COP antibodies.

Arrowheads point to budding COPI-coated vesicles. Bars = 100 nm.

KI Dissociation of COPI- and COPII-Coat Proteins from Cauliflower Inflorescence Membranes.

(A) A Golgi-enriched fraction was treated with increasing concentrations of KI, as described in Methods, and then centrifuged to separate the membranes from the extraction medium. The pelleted membranes were then probed for the presence of coat proteins.

(B) Golgi-enriched membranes were treated as in (A), but with 300 mM KI, and then were probed with GTPase antisera. Lane 1, native membranes; lane 2, KI-stripped membranes.

In Vitro Recruitment of Cytosolic COPI-Vesicle Coat Proteins onto KI-Stripped Membranes.

(A) Recruitment of GTPases onto cauliflower membranes. KI-stripped membranes were incubated with cytosol, ATP-regenerating system, and GTPγS for 25 min at 20°C. Membranes with bound proteins were separated from unbound proteins by centrifugation. Small GTPases in each fraction were detected in a protein gel blot with specific antibodies against AtArf1p and AtSar1p. Lane 1 contains KI-stripped membranes before incubation with cytosolic proteins; lane 2, the supernatant after recruitment; and lane 3, the pelleted membranes after recruitment.

(B) Selective recruitment of coatomer onto cauliflower membranes. KI-stripped membranes were incubated as described in (A), and the sediment and supernatant proteins were screened by protein gel blotting with Atγ-COP and AtSec23p antibodies. Lane 1 contains native membranes; lane 2, KI-stripped membranes; lane 3, cytosolic proteins; lane 4, supernatant after recruitment; and lane 5, pelleted membranes after recruitment.

(C) Absence of precipitable Atγ-COP, AtArf1p, AtSec23p, and AtSar1p in cytosol only (left). Nonsaturation of coat protein recruitments onto cauliflower membranes (right). The ratio of cytosolic:membrane proteins in the recruitment assay was increased by 30% (lanes 1 and 4), 100% (lanes 2 and 5), and 200% (lanes 3 and 6) over the standard values (6 mg mL^–1:0.2 mg L^–1). Lanes 1 to 3 represent the supernatant fractions after recruitment; lanes 4 to 6, the corresponding pelleted membrane fractions. S represents the supernatant, P the pellet after recruitment in the absence of membranes. Membranes, medium, incubation, and other conditions were as described in (A). Antibody screening was as described in (A) and (B).

(D) Heterologous recruitment of COPI-vesicle coat proteins from cauliflower cytosol onto Golgi/ER membranes from tobacco mesophyll. Tobacco membranes were isolated as described in Methods, incubated with cauliflower cytosol, and subsequently screened with antibodies under the conditions used in (A). Lane 1 contains KI-stripped membranes; lane 2, pelleted membranes after recruitment.

BFA Inhibits Recruitment of Coatomer and AtArf1p in Cauliflower Recruitment Assay.

Bound coatomer/Arf1p in control and BFA-treated samples was quantified by densitometry of protein gel blots of samples of equal volume. Shown are the results of four separate experiments whose average is given as columns; the error bars represent the extent of the variation between experiments. (+) denotes the presence of 300 μM BFA and (–) the absence of BFA in the incubation media.

Detection of in Vitro–Formed COPI-Coated Vesicles.

(A) Recruitment of coatomer onto KI-stripped membranes leads to an increase in their equilibrium density. Stripped membranes from cauliflower inflorescence were incubated in the absence or presence of cauliflower cytosolic proteins, as described for Figure 6A. The incubation mixtures were then layered onto sucrose density gradients and centrifuged to equilibrium, as described in Methods. Fractions were screened with antibodies against ER (calnexin, BiP), Golgi (RGP), and COPI/COPII coat proteins (Atγ-COP, AtSec23p). As depicted, stripped membranes banded at densities ∼10% (w/w) less than those at which the recruited membranes did.

(B) Isolation of COPI-coated vesicles. KI-stripped cauliflower membranes were incubated with cauliflower cytosol under standard conditions, extracted with high-salt reagent (250 mM KCl) for 30 min at 4°C, and centrifuged at 30,000g; the membranes in the supernatant were subjected to isopcynic sucrose density gradient centrifugation as in (A). Equal-volume fractions were then monitored in protein gel blots with the antisera described above. The asterisk denotes the putative COPI-coated vesicle–containing fraction used for Figure 9.

Immunogold Negative Staining of the Contents of Fraction 12 from the Gradient Shown in Figure 8B.

(A) Overview of normal negative staining. Putative COPI-coated vesicles are indicated with arrowheads, clathrin-coated vesicles with arrows.

(B) Comparison of clathrin- and COP-coated vesicles. Arrows and arrowheads are as in (A).

(C) to (J) Gallery of negatively stained putative COPI-coated vesicles decorated with gold-coupled Zmε-COP antibodies.

Bar in (A) = 1 μm; bar in (B) = 100 nm; bar in (J) = 100 nm for (C) to (J).