Vesiculation and sorting from PC12-derived endosomes in vitro

被引:53
作者
Lichtenstein, Y
Desnos, C
Faúndez, V
Kelly, RB [1 ]
Clift-O'Grady, L
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Hormone Res Inst, San Francisco, CA 94143 USA
关键词
D O I
10.1073/pnas.95.19.11223
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Formation of small vesicles resembling synaptic vesicles can be reconstituted in vitro by incubating labeled homogenates of PC12 cells with ATP and two cytoplasmic proteins, AP3 and ARF1 [Faundez, V., Horng, J.-T. Sr Kelly, R. B. (1998) Cell 93, 423-432], To determine whether AP3 was mediating budding from plasma membranes or endosomes the organelle that generated the synaptic vesicles was characterized. The budding activity was enriched in organelles that labeled at 15 degrees C, but not at 4 degrees C, that excluded a marker of plasma membranes and that contained internalized transferrin, indicating that the precursor was an endosome. Vesicles formed from the endosomal precursor in vitro excluded transferrin, We conclude that ARF-mediated vesiculation into synaptic vesicle-sized organelles uses an endosomal precursor and occurs simultaneously in vitro with sorting of synaptic vesicle proteins from other membrane protein constituents of the endosome.
引用
收藏
页码:11223 / 11228
页数:6
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