Insights into secretory and endocytic membrane traffic using green fluorescent protein chimeras

被引:47
作者
LippincottSchwartz, J [1 ]
Smith, CL [1 ]
机构
[1] NINCDS, NIH, BETHESDA, MD 20892 USA
关键词
D O I
10.1016/S0959-4388(97)80082-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Green fluorescent fusion proteins, which can be visualized in the unperturbed environment of a living cell, have become important reporter molecules for studying protein localization and trafficking within secretory and endocytic membranes of living cells. They have been used in a wide variety of applications, including time-lapse imaging, double-labeling and photobleach experiments. Results from such work are clarifying the steps involved in the formation, translocation and fusion of transport intermediates, are defining the roles for microtubules in membrane transport, and are providing insights into the mechanisms of protein retention and localization within organelles. In so doing, they have changed our thinking about the temporal and spatial relationships between subcellular membrane structures and the morphogenesis of secretory and endocytic organelles.
引用
收藏
页码:631 / 639
页数:9
相关论文
共 64 条
  • [61] Spatial dynamics of GFP-tagged proteins investigated by local fluorescence enhancement
    Yokoe, E
    Meyer, T
    [J]. NATURE BIOTECHNOLOGY, 1996, 14 (10) : 1252 - 1256
  • [62] ZAAL KJM, 1996, MOL BIOL CELL, V7, P321
  • [63] Rab GTPases in vesicular transport
    Zerial, Marino
    Stenmark, Harald
    [J]. CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (04) : 613 - 620
  • [64] A ''humanized'' green fluorescent protein cDNA adapted for high-level expression in mammalian cells
    Zolotukhin, S
    Potter, M
    Hauswirth, WW
    Guy, J
    Muzyczka, N
    [J]. JOURNAL OF VIROLOGY, 1996, 70 (07) : 4646 - 4654