Coat assembly directs v-SNARE concentration into synthetic COPII vesicles
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作者:
Matsuoka, K
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机构:Univ Calif Berkeley, Howard Hughes Med Inst, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Matsuoka, K
Morimitsu, Y
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机构:Univ Calif Berkeley, Howard Hughes Med Inst, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Morimitsu, Y
Uchida, K
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机构:Univ Calif Berkeley, Howard Hughes Med Inst, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Uchida, K
Schekman, R
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Univ Calif Berkeley, Howard Hughes Med Inst, Dept Cell & Mol Biol, Berkeley, CA 94720 USAUniv Calif Berkeley, Howard Hughes Med Inst, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
Schekman, R
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机构:
[1] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Cell & Mol Biol, Berkeley, CA 94720 USA
[2] Nagoya Univ, Lab Food & Biodynam, Nagoya, Aichi 4648601, Japan
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.