Coat Assembly Directs v-SNARE Concentration into Synthetic COPII Vesicles
pmid: 9844642
Coat Assembly Directs v-SNARE Concentration into Synthetic COPII Vesicles
COPII proteins are required to create transport vesicles and to select cargo molecules for transit from the ER. A reconstituted liposome budding reaction was used to detect the capture and concentration of membrane-associated v-SNARE molecules into synthetic COPII vesicles. A novel glutathione-phosphatidyl-ethanolamine conjugate (Glut-PE) was synthesized and incorporated into chemically defined liposomes to provide binding sites for GST hybrid proteins. Large liposomes containing bound cytoplasmic domains of the v-SNAREs, Sec22p or Bos1p, or of the ER resident proteins, Sec12p and Ufe1p, were exposed to COPII proteins and GMP-PNP. v-SNAREs but not resident proteins were concentrated in synthetic COPII vesicles generated from donor liposomes. We conclude that COPII proteins are necessary and sufficient for cargo selection and vesicle morphogenesis.
- Howard Hughes Medical Institute United States
- Nagoya University Japan
- University of California, Berkeley United States
Cytoplasm, Membrane Glycoproteins, Qa-SNARE Proteins, Phosphatidylethanolamines, Coated Vesicles, Membrane Proteins, Biological Transport, Receptors, Cell Surface, Cell Biology, Qb-SNARE Proteins, Phosphoproteins, Glutathione, Fungal Proteins, R-SNARE Proteins, Cross-Linking Reagents, Liposomes, Centrifugation, Density Gradient, Guanine Nucleotide Exchange Factors, Chromatography, Thin Layer, Carrier Proteins, Molecular Biology, Glutathione Transferase
Cytoplasm, Membrane Glycoproteins, Qa-SNARE Proteins, Phosphatidylethanolamines, Coated Vesicles, Membrane Proteins, Biological Transport, Receptors, Cell Surface, Cell Biology, Qb-SNARE Proteins, Phosphoproteins, Glutathione, Fungal Proteins, R-SNARE Proteins, Cross-Linking Reagents, Liposomes, Centrifugation, Density Gradient, Guanine Nucleotide Exchange Factors, Chromatography, Thin Layer, Carrier Proteins, Molecular Biology, Glutathione Transferase
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