Visualization of ER-to-Golgi Transport in Living Cells Reveals a Sequential Mode of Action for COPII and COPI
暂无分享,去创建一个
[1] W. Hong,et al. Protein transport from the endoplasmic reticulum to the Golgi apparatus. , 1998, Journal of cell science.
[2] R. Schekman,et al. Does COPI Go Both Ways? , 1997, Cell.
[3] J. Rothman,et al. Bidirectional Transport by Distinct Populations of COPI-Coated Vesicles , 1997, Cell.
[4] R. Pepperkok,et al. Dissociation of Coatomer from Membranes Is Required for Brefeldin A–induced Transfer of Golgi Enzymes to the Endoplasmic Reticulum , 1997, The Journal of cell biology.
[5] S. Emr,et al. COPI-independent Anterograde Transport: Cargo-selective ER to Golgi Protein Transport in Yeast COPI Mutants , 1997, The Journal of cell biology.
[6] B. Tang,et al. The mammalian homolog of yeast Sec13p is enriched in the intermediate compartment and is essential for protein transport from the endoplasmic reticulum to the Golgi apparatus , 1997, Molecular and cellular biology.
[7] W. Balch,et al. The organization of endoplasmic reticulum export complexes , 1996, The Journal of cell biology.
[8] J. Rothman,et al. Protein Sorting by Transport Vesicles , 1996, Science.
[9] F. Gu,et al. An endosomal beta COP is involved in the pH-dependent formation of transport vesicles destined for late endosomes , 1996, The Journal of cell biology.
[10] J. Lippincott-Schwartz,et al. Golgi dispersal during microtubule disruption: regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites. , 1996, Molecular biology of the cell.
[11] P. Cosson,et al. Delta‐ and zeta‐COP, two coatomer subunits homologous to clathrin‐associated proteins, are involved in ER retrieval. , 1996, The EMBO journal.
[12] R. Schekman,et al. Coat Proteins and Vesicle Budding , 1996, Science.
[13] R. Schekman,et al. COPI- and COPII-coated vesicles bud directly from the endoplasmic reticulum in yeast , 1995, Cell.
[14] T. Kreis,et al. In Vitro Assembly and Disassembly of Coatomer (*) , 1995, The Journal of Biological Chemistry.
[15] H. Nomoto,et al. Anterograde and retrograde traffic between the rough endoplasmic reticulum and the Golgi complex , 1995, The Journal of cell biology.
[16] I. Mellman,et al. Cytoplasmic coat proteins involved in endosome function , 1995, Cell.
[17] W. Balch,et al. Sequential coupling between COPII and COPI vesicle coats in endoplasmic reticulum to Golgi transport , 1995, The Journal of cell biology.
[18] R. Pepperkok,et al. Immunocytochemical localization of beta-COP to the ER-Golgi boundary and the TGN. , 1995, Journal of cell science.
[19] N. Narula,et al. Distinct coated vesicles labeled for p200 bud from trans-Golgi network membranes. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[20] L. Orci,et al. Human SEC13Rp functions in yeast and is located on transport vesicles budding from the endoplasmic reticulum , 1995, The Journal of cell biology.
[21] H. Pelham. About turn for the COPs? , 1994, Cell.
[22] S. Emr,et al. Coatomer is essential for retrieval of dilysine-tagged proteins to the endoplasmic reticulum , 1994, Cell.
[23] R. Schekman,et al. Coatomer-rich endoplasmic reticulum. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[24] B. Goud,et al. Localization of the Lys, Asp, Glu, Leu tetrapeptide receptor to the Golgi complex and the intermediate compartment in mammalian cells , 1994, The Journal of cell biology.
[25] R. Schekman,et al. Yeast beta- and beta'-coat proteins (COP). Two coatomer subunits essential for endoplasmic reticulum-to-Golgi protein traffic. , 1994, The Journal of biological chemistry.
[26] A. Helenius,et al. Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus , 1994, The Journal of cell biology.
[27] R. Schekman,et al. COPII: A membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum , 1994, Cell.
[28] M. Krieger,et al. Disruptions in Golgi structure and membrane traffic in a conditional lethal mammalian cell mutant are corrected by epsilon-COP , 1994, The Journal of cell biology.
[29] W. Balch,et al. Rab1 and Ca2+ are required for the fusion of carrier vesicles mediating endoplasmic reticulum to Golgi transport , 1994, The Journal of cell biology.
[30] P. Cosson,et al. Coatomer interaction with di-lysine endoplasmic reticulum retention motifs. , 1994, Science.
[31] W. Balch,et al. Vesicular stomatitis virus glycoprotein is sorted and concentrated during export from the endoplasmic reticulum , 1994, Cell.
[32] T. Suganuma,et al. A protein-specific monoclonal antibody to rat liver beta 1-->4 galactosyltransferase and its application to immunohistochemistry. , 1994, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[33] W. Balch,et al. Dominant inhibitory mutants of ARF1 block endoplasmic reticulum to Golgi transport and trigger disassembly of the Golgi apparatus. , 1994, The Journal of biological chemistry.
[34] P. Rottier,et al. Characterization of the budding compartment of mouse hepatitis virus: evidence that transport from the RER to the Golgi complex requires only one vesicular transport step , 1994, The Journal of cell biology.
[35] W. Balch,et al. Beta-COP is essential for transport of protein from the endoplasmic reticulum to the Golgi in vitro , 1993, The Journal of cell biology.
[36] R. Pepperkok,et al. β-COP is essential for biosynthetic membrane transport from the endoplasmic reticulum to the Golgi complex in vivo , 1993, Cell.
[37] J. Rothman,et al. Binding of coatomer to Golgi membranes requires ADP-ribosylation factor. , 1993, The Journal of biological chemistry.
[38] J. Rothman,et al. Budding from Golgi membranes requires the coatomer complex of non-clathrin coat proteins , 1993, Nature.
[39] M. Jackson,et al. Retrieval of transmembrane proteins to the endoplasmic reticulum , 1993, The Journal of cell biology.
[40] J. Slot,et al. Beta-COP localizes mainly to the cis-Golgi side in exocrine pancreas , 1993, The Journal of cell biology.
[41] J. Lippincott-Schwartz. Bidirectional membrane traffic between the endoplasmic reticulum and Golgi apparatus. , 1993, Trends in cell biology.
[42] S. Wong,et al. Molecular cloning, characterization, subcellular localization and dynamics of p23, the mammalian KDEL receptor , 1993, The Journal of cell biology.
[43] H. Hauri,et al. The endoplasmic reticulum—Golgi intermediate compartment , 1992, Current Biology.
[44] M. Torrisi,et al. Immunocytochemical analysis of the transfer of vesicular stomatitis virus G glycoprotein from the intermediate compartment to the Golgi complex , 1992, The Journal of cell biology.
[45] N. Narula,et al. Identification of a 200-kD, brefeldin-sensitive protein on Golgi membranes , 1992, The Journal of cell biology.
[46] J. Saraste,et al. Distribution of the intermediate elements operating in ER to Golgi transport. , 1991, Journal of cell science.
[47] R. Schekman,et al. Mammalian Sec23p homologue is restricted to the endoplasmic reticulum transitional cytoplasm. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[48] M. Roth,et al. A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin , 1991, The Journal of cell biology.
[49] H. Hauri,et al. The isolated ER-Golgi intermediate compartment exhibits properties that are different from ER and cis-Golgi , 1991, The Journal of cell biology.
[50] J. Lippincott-Schwartz,et al. Brefeldin A, a drug that blocks secretion, prevents the assembly of non-clathrin-coated buds on Golgi cisternae , 1991, Cell.
[51] P. Argos,et al. β-COP, a 110 kd protein associated with non-clathrin-coated vesicles and the golgi complex, shows homology to β-adaptin , 1991, Cell.
[52] J. Lippincott-Schwartz,et al. Dissociation of a 110-kD peripheral membrane protein from the Golgi apparatus is an early event in brefeldin A action , 1990, The Journal of cell biology.
[53] H. Hauri,et al. Identification of an intermediate compartment involved in protein transport from endoplasmic reticulum to Golgi apparatus. , 1990, European journal of cell biology.
[54] R. Schekman,et al. Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway , 1990, Cell.
[55] J. Lippincott-Schwartz,et al. Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin a suggests an ER recycling pathway , 1990, Cell.
[56] J. Rothman,et al. Purification of a novel class of coated vesicles mediating biosynthetic protein transport through the Golgi stack , 1989, Cell.
[57] J. Lippincott-Schwartz,et al. Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: Evidence for membrane cycling from Golgi to ER , 1989, Cell.
[58] H. Hauri,et al. Identification, by a monoclonal antibody, of a 53-kD protein associated with a tubulo-vesicular compartment at the cis-side of the Golgi apparatus , 1988, The Journal of cell biology.
[59] T. Kreis,et al. Microtubules containing detyrosinated tubulin are less dynamic. , 1987, The EMBO journal.
[60] K. Simons,et al. The trans Golgi network: sorting at the exit site of the Golgi complex. , 1986, Science.
[61] H. Lodish,et al. Oligomerization is essential for transport of vesicular stomatitis viral glycoprotein to the cell surface , 1986, Cell.
[62] J. Rose,et al. A single amino acid substitution in a hydrophobic domain causes temperature-sensitive cell-surface transport of a mutant viral glycoprotein , 1985, Journal of virology.
[63] E. Kuismanen,et al. Pre- and post-golgi vacuoles operate in the transport of semliki forest virus membrane glycoproteins to the cell surface , 1984, Cell.
[64] S. Singer,et al. Effect of microtubule assembly status on the intracellular processing and surface expression of an integral protein of the plasma membrane , 1984, The Journal of cell biology.
[65] S. Singer,et al. Immunoelectron microscopic studies of the intracellular transport of the membrane glycoprotein (G) of vesicular stomatitis virus in infected Chinese hamster ovary cells , 1983, The Journal of cell biology.
[66] R. Schekman,et al. Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway , 1980, Cell.
[67] I. Mellman. Endocytosis and molecular sorting. , 1996, Annual review of cell and developmental biology.
[68] S Falkow,et al. FACS-optimized mutants of the green fluorescent protein (GFP). , 1996, Gene.
[69] F. Maxfield,et al. Membrane transport in the endocytic pathway. , 1995, Current opinion in cell biology.
[70] A. Helenius,et al. Quality control in the secretory pathway. , 1995, Current opinion in cell biology.
[71] R. Pepperkok,et al. Immunocytochemical localization of β-COP to the ER-Golgi boundary and the TGN , 1995 .
[72] R. Pepperkok,et al. COPs regulating membrane traffic. , 1995, Annual review of cell and developmental biology.
[73] R. Vallee,et al. DYNEINS: molecular structure and cellular function. , 1994, Annual review of cell biology.