Dynamin, endocytosis and intracellular signalling (Review)

REFERENCES

• Ahle S., Ungewickell E. Purification and properties of a new clathrin assembly protein. EMBO Journal 1986; 5: 3143–3149
   PubMedGoogle Scholar
• Aimers W., Tse F. W. Transmitter release from synapses: does a preassembled fusion pore initiate exocytosis. Neuron 1990; 4: 813–818
   PubMedGoogle Scholar
• Alvarez De, Toledo G., FernandezChacon R., Fernandez J. M. Release of secretory products during transient vesicle fusion. Nature 1993; 363: 554–558
   PubMedGoogle Scholar
• Ando A., Yonezawa K., Gout I., Nakata T., Ueda H., Hara K., Kitamura Y., Noda Y., Takenawa T., Hirokawa N., Waterfield M. D., Kasuga M. A complex of GRB2-dynamin binds to tyrosine-phosphorylated insulin receptor substrate-1 after insulin treatment. EMBO Journal 1994; 13: 3033–3038
   PubMed Web of Science ®Google Scholar
• Artalejo C. R., Henley J. R., McNiven M. A., Palfrey H. C. Rapid endocytosis coupled to exocytosis in adrenal chromaffin cells involves Ca2+, GTP, and dynamin but not clathrin. Proceedings of the National Academy of Sciences, USA 1995; 92: 8328–8332
   PubMedGoogle Scholar
• Artalejo C. R., Elhamdani A., Palfrey H. C. Calmodulin is the divalent cation receptor for rapid endocytosis, but not exocytosis, in adrenal chromaffin cells. Neuron 1996; 16: 195–205
   PubMedGoogle Scholar
• Bailly E., McCaffrey M., Touchot N., Zahraoui A., Goud B., Bornens M. Phosphorylation of two small GTP-binding proteins of the Rab family by p34cdc2. Nature 1991; 350: 715–718
   PubMed Web of Science ®Google Scholar
• Bajjalieh S. M., Scheller R. H. The biochemistry of neurotransmitter secretion. Journal of Biological Chemistry 1995; 270: 1971–1974
   PubMed Web of Science ®Google Scholar
• Bazzi M. D., Nelsestuen G. L. Protein kinase C and annexins: unusual calcium response elements in the cell. Cellular Signalling 1993; 5: 357–365
   PubMedGoogle Scholar
• Beck K. A., Keen J. H. Interaction of phosphoinositide cycle intermediates with the plasma membrane-associated clathrin assembly protein AP-2. Journal of Biological Chemistry 1991; 266: 4442–4447
   PubMedGoogle Scholar
• Betz W. J., Bewick G. S. Optical analysis of synaptic vesicle recycling at the frog neuromuscular junction. Science 1992; 255: 200–203
   PubMedGoogle Scholar
• Betz W. J., Bewick G. S. Optical monitoring of transmitter release and synaptic vesicle recycling at the frog neuromuscular junction. Journal of Physiology (London) 1993; 460: 287–309
   PubMedGoogle Scholar
• Bittner M. A., Bennett M. K., Holz R. W. Evidence that syntaxin 1A is involved in storage in the secretory pathway. Journal of Biological Chemistry 1996; 271: 11214–11221
   PubMedGoogle Scholar
• Booker G. W., Gout I., Downing A. K., Driscoll P. C., Boyd J., Waterfield M. D., Campbell I. D. Solution structure and ligand-binding site of the SH3 domain of the p85-alpha subunit of phosphatidylinositol 3-kinase. Cell 1993; 73: 813–822
   PubMedGoogle Scholar
• Burgoyne R. D., Morgan A. Regulated exocytosis. Biochemical Journal 1993; 293: 305–316
   PubMed Web of Science ®Google Scholar
• Burns M. E., Augustine G. J. Synaptic structure and function: dynamic organization yields architectural precision. Cell 1996; 83: 187–194
   Google Scholar
• Ceccaldi P. E., Grohovaz F., Benfenati F., Chieregatti E., Greengard P., Valtorta F. Dephosphorylated synapsin I anchors synaptic vesicles to actin cytoskeleton: an analysis by videomicroscopy. Journal of Cell Biology 1995; 128: 905–912
   PubMed Web of Science ®Google Scholar
• Ceccarelli B., Hurlbut W. P. Ca2+-dependent recycling of synaptic vesicles at the frog neuromuscular junction. Journal of Cell Biology 1980; 57: 499–524
   Google Scholar
• Ceccarelli B., Hurlbut W. P. Vesicle hypothesis of the release of quanta of acetylcholine. Physiological Reviews 1980; 60: 396–441
   PubMed Web of Science ®Google Scholar
• Ceccarelli B., Hurlbut W. P., Mauro A. Depletion of vesicles from frog neuromuscular junctions by prolonged tetanic stimulation. Journal of Cell Biology 1972; 54: 30–38
   PubMed Web of Science ®Google Scholar
• Ceccarelli B., Hurlbut W. P., Mauro A. Turnover of transmitter and synaptic vesicles at the frog neuromuscular junction. Journal of Cell Biology 1973; 7: 499–524
   Google Scholar
• Chen M. S., Obar R. A., Schroeder C. C., Austin T. W., Poodry C. A., Wadsworth S. C., Vallee R. B. Multiple forms of dynamin are encoded by shibire, a Drosophila gene involved in endocytosis. Nature 1991; 351: 583–586
   PubMed Web of Science ®Google Scholar
• Colasante C., Pecot-Dechavassine M. Ultrastructural distribution of synaptophysin and synaptic vesicle recycling at the frog neuromuscular junction. Journal of Neuroscience Research 1996; 44: 272–282
   PubMedGoogle Scholar
• Cook T. A., Urrutia R., McNiven M. A. Identification of dynamin 2, an isoform ubiquitously expressed in rat tissues. Proceedings of the National Academy of Sciences, USA 1994; 91: 644–648
   PubMedGoogle Scholar
• Damke H., Baba T., Warnock D. E., Schmid S. L. Induction of mutant dynamin specifically blocks endocytic coated vesicle formation. Journal of Cell Biology 1994; 127: 915–934
   PubMedGoogle Scholar
• Damke H., Baba T., van derBliek A. M., Schmid S. L. Clathrin-independent pinocytosis is induced in cells overexpressing a temperature-sensitive mutant of dynamin. Journal of Cell Biology 1995; 131: 69–80
   PubMedGoogle Scholar
• David C., McPherson P. S., Mundigl O., De Camilli P. A role of amphiphysin in synaptic vesicle endocytosis suggested by its binding to dynamin in nerve terminals. Proceedings of the National Academy of Sciences, USA 1996; 93: 331–335
   PubMed Web of Science ®Google Scholar
• DeCamilli P., Takei K. Molecular mechanisms in synaptic vesicle endocytosis and recycling. Neuron 1996; 16: 481–486
   PubMedGoogle Scholar
• DeCamilli P., Thomas A., Cofiell R., Folli F., Lichte B., Piccolo G., Meinck H. M., Austoni M., Fassetta G., Bottazzo G., Bates D., Cartlidge N., Solimena M., Kilimann M. W. The synaptic vesicle-associated protein amphiphysin is the 128-kD autoantigen of Stiff-Man syndrome with breast cancer. Journal of Experimental Medicine 1993; 178: 2219–2223
   PubMedGoogle Scholar
• Diatloff-Zito C., Gordon A. J. E., Duchaud E., Merlin G. Isolation of an ubiquitously expressed cDNA encoding human dynamin II, a member of the large GTP-binding protein family. Gene 1995; 163: 301–306
   PubMedGoogle Scholar
• Dropcho E. J. Antiamphiphysin antibodies with small-cell lung carcinoma and paraneoplastic encephalomyelitis. Annals of Neurology 1996; 39: 659–667
   PubMed Web of Science ®Google Scholar
• Duden R., Hosobuchi M., Hamamoto S., Winey M., Byers B., Schekman R. Yeast beta-and beta-coat proteins (COP). Two coatomer subunits essential for endoplasmic reticulum-to-Golgi protein traffic. Journal of Biological Chemistry 1994; 269: 24486–24495
   PubMedGoogle Scholar
• Dynlacht B. D., Weinzierl R. O., Admon A., Tjian R. The dTAFII8O subunit of Drosophila TFIID contains beta-transducin repeats. Nature 1993; 363: 176–179
   PubMedGoogle Scholar
• Engisch K. L., Nowycky M. C. Calcium dependence of large dense-cored vesicle exocytosis evoked by calcium influx in bovine adrenal chromaffin cells. Journal of Neuroscience 1996; 16: 1359–1369
   PubMedGoogle Scholar
• Fantl W. J., Johnson D. E., Williams L. T. Signalling by receptor tyrosine kinases. Annual Review of Biochemistry 1993; 62: 453–481
   PubMed Web of Science ®Google Scholar
• Ferguson K. M., Lemmon M. A., Schlessinger J., Sigler P. B. Crystal structure at 2.2 A resolution of the pleckstrin homology domain from human dynamin. Cell 1994; 79: 199–209
   PubMed Web of Science ®Google Scholar
• Fesce R., Grohovaz F., Valtorta F., Meldolesi J. Neurotransmitter release: fusion or ‘kiss-and-run'?. Trends in Cell Biology 1994; 4: 1–4
   PubMedGoogle Scholar
• Gammie A. E., Kurihara L. J., Vallee R. B., Rose M. D. DNM1, a dynamin-related gene, participates in endosomal trafficking in yeast. Journal of Cell Biology 1995; 130: 553–566
   PubMedGoogle Scholar
• Gass G. V., Lin J. J. C., Scaife R., Wu C. F. Two isoforms of Drosophila dynamin in wild-type and shibirets neural tissue: different subcellular localization and association mechanisms. Journal of Neurogenetics 1995; 10: 169–191
   PubMed Web of Science ®Google Scholar
• Geppert M., Goda Y., Hammer R. E., Li C., Rosahl T. W., Stevens C. F., Südhof T. C. Synaptotagmin I: a major Ca2+ sensor for transmitter release at a central synapse. Cell 1994; 79: 717–727
   PubMed Web of Science ®Google Scholar
• Gerich B., Orci L., Tschochner H., Lottspeich F., Ravazzola M., Amherdt M., Wieland F., Harter C. Non-clathrin-coat protein alpha is a conserved subunit of coatomer and in Saccharomyces cerevisiae is essential for growth. Proceedings of the National Academy of Sciences, USA 1995; 92: 3229–3233
   PubMedGoogle Scholar
• Gilboa L., Ben-Levy R., Yarden Y., Henis Y. I. Roles for a cytoplasmic tyrosine and tyrosine kinase activity in the interactions of Neu receptors with coated pits. Journal of Biological Chemistry 1995; 270: 7061–7067
   PubMed Web of Science ®Google Scholar
• Goldsmith E. J., Cobb M. H. Protein kinases. Current Opinion in Structural Biology 1994; 4: 833–840
   PubMed Web of Science ®Google Scholar
• Gout I., Dhand R., Hiles I. D., Fry M. J., Panayotou G., Das P., Truong O., Totty N. F., Hsuan J., Booker G. W., Campbell I. D., Waterfield M. D. The GTPase dynamin binds to and is activated by a subset of SH3 domains. Cell 1993; 75: 25–36
   PubMed Web of Science ®Google Scholar
• Gu X., Verma D. P. S. Phragmoplastin, a dynamin-like protein associated with cell plate formation in plants. EMBO Journal 1996; 15: 695–704
   PubMedGoogle Scholar
• Guan K., Farh L., Marshall T. K., Deschenes R. J. Normal mitochondrial structure and genome maintenance in yeast requires the dynamin-like product of the MGM1 gene. Current Genetics 1993; 24: 141–148
   PubMedGoogle Scholar
• Harris K. M., Stevens J. K. Dendritic spines of CA1 pyramidal cells in the rat hippocampus: serial electron microscopy with reference to their biophysical characteristics. Journal of Neuroscience 1989; 9: 2982–2997
   PubMed Web of Science ®Google Scholar
• Haslam R. J., Koide H. B., Hemmings B. A. Pleckstrin domain homology. Nature 1993; 363: 309–310
   PubMed Web of Science ®Google Scholar
• Henkel A. W., Betz W. J. Staurosporine blocks evoked release of FM1–43 but not acetylcholine from frog motor nerve terminals. Journal of Neuroscience 1995; 15: 8246–8258
   PubMedGoogle Scholar
• Henkel A. W., Betz W. J. Monitoring of Black Widow Spider Venom (BWSV) induced exo-and endocytosis in living frog motor nerve terminals with FM1–43. Neuropharmacology 1995; 34: 1397–1406
   PubMedGoogle Scholar
• Henley J. R., McNiven M. A. Association of a dynamin-like protein with the golgi apparatus in mammalian cells. Journal of Cell Biology 1996; 133: 761–775
   PubMed Web of Science ®Google Scholar
• Herskovits J. S., Burgess C. C., Obar R. A., Vallee R. B. Effects of mutant rat dynamin on endocytosis. Journal of Cell Biology 1993; 122: 565–578
   PubMedGoogle Scholar
• Herskovits J. S., Shpetner H. S., Burgess C. C., Vallee R. B. Microtubules and Src homology 3 domains stimulate the dynamin GTPase via its C-terminal domain. Proceedings of the National Academy of Sciences, USA 1993; 90: 11468–11472
   PubMedGoogle Scholar
• Heuser J. The role of coated vesicles in recycling of synaptic vesicle membrane. Cell Biology International Report 1989; 13: 1063–1076
   PubMedGoogle Scholar
• Heuser J. E., Reese T. S. Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction. Journal of Cell Biology 1973; 57: 315–344
   PubMedGoogle Scholar
• Hinshaw J. E., Schmid S. L. Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding. Nature 1995; 374: 190–192
   PubMed Web of Science ®Google Scholar
• Hirokawa N., Sobue K., Kanda K., Harada A., Yorifuji H. The cytoskeletal architecture of the presynaptic terminal and molecular structure of synapsin 1. Journal of Cell Biology 1989; 108: 111–126
   PubMed Web of Science ®Google Scholar
• Hosoya H., Komatsu S., Shimizu T., Inagaki M., Ikegami M., Yazaki K. Phosphorylation of dynamin by cdc2 kinase. Biochemical and Biophysical Research Communications 1994; 202: 1127–1133
   PubMedGoogle Scholar
• House C., Kemp B. E. Protein kinase C contains a pseudosubstrate prototope in its regulatory domain. Science 1987; 238: 1726–1728
   PubMed Web of Science ®Google Scholar
• Ingley E., Hemmings B. A. Pleckstrin homology (PH) domains in signal transduction. Journal of Cellular Biochemistry 1994; 56: 436–443
   PubMedGoogle Scholar
• Jahn R., Sudhof T. C. Synaptic vesicles and exocytosis. Annual Review of Neuroscience 1994; 17: 219–246
   PubMedGoogle Scholar
• Jaken S. Protein kinase C isozymes and substrates. Current Opinion in Cell Biology 1996; 8: 168–173
   PubMed Web of Science ®Google Scholar
• Jones B. A., Fangman W. L. Mitochondrial DNA maintenance in yeast requires a protein containing a region related to the GTP-binding domain of dynamin. Genes and Development 1992; 6: 380–389
   PubMedGoogle Scholar
• Kadota T., Mizote M., Kadota K. Dynamics of presynaptic endosomes produced during transmitter release. Journal of Electron Microscopy, Tokyo 1994; 43: 62–71
   PubMedGoogle Scholar
• Kelly R. B. Storage and release of neurotransmitters. Cell 1993; 72 (Suppl.): 43–53
   PubMedGoogle Scholar
• Kelly R. B. Neural transmission: synaptotagmin is just a calcium sensor. Current Biology 1995; 5: 257–259
   PubMedGoogle Scholar
• Kharbanda S., Saleem A., Yuan Z., Emoto Y., Prasad K. V., Kufe D. Stimulation of human monocytes with macrophage colony-stimulating factor induces a Grb2-mediated association of the focal adhesion kinase pp125FAK and dynamin. Proceedings of the National Academy of Sciences, USA 1995; 92: 6132–6136
   PubMed Web of Science ®Google Scholar
• Koch C. A., Anderson D., Moran M. F., Ellis C., Pawson T. SH2 and SH3 domains: elements that control interactions of cytoplasmic signaling proteins. Science 1991; 252: 668–674
   PubMed Web of Science ®Google Scholar
• Koenig J. H., Ikeda K. Disappearance and reformation of synaptic vesicle membrane upon transmitter release observed under reversible blockage of membrane retrieval. Journal of Neuroscience 1989; 9: 3844–3860
   PubMed Web of Science ®Google Scholar
• Konishi H., Kuroda S., Kikkawa U. The pleckstrin homology domain of rac protein kinase associates with the regulatory domain of protein kinase C zeta. Biochemical and Biophysical Research Communications 1994; 205: 1770–1775
   PubMedGoogle Scholar
• Konishi H., Shinomura T., Kuroda S., Ono Y., Kikkawa U. Molecular cloning of rat RAC protein kinase aP and β and their association with protein kinase C zeta. Biochemical and Biophysical Research Communications 1994; 205: 817–825
   PubMedGoogle Scholar
• Konishi H., Kuroda S., Tanaka M., Matsuzaki H., Ono Y., Kameyama K., Haga T., Kikkawa U. Molecular cloning and characterization of a new member of the RAC protein kinase family: Association of the pleckstrin homology domain of three types of RAC protein kinase with protein kinase C subspecies and βsG subunits of G proteins. Biochemical and Biophysical Research Communications 1995; 216: 526–534
   PubMedGoogle Scholar
• Kosaka T., Ikeda K. Possible temperature-dependent blockage of synaptic vesicle recycling induced by a single gene mutation in Drosophila. Journal of Neurobiology 1983; 14: 207–225
   PubMedGoogle Scholar
• Krueger B. K., Forn J., Greengard P. Depolarization-induced phosphorylation of specific proteins, mediated by calcium ion influx, in rat brain synaptosomes. Journal of Biological Chemistry 1977; 252: 2764–2773
   PubMed Web of Science ®Google Scholar
• Lamaze C., Schmid S. L. The emergence of clathrin-independent pinocytic pathways. Current Opinion in Cell Biology 1995; 7: 573–580
   PubMed Web of Science ®Google Scholar
• Leveque C., ElFar O., Martin-Moutot N., Sato K., Kato R., Takahashi M., Seagar M. J. Purification of the N-type calcium channel associated with syntaxin and synaptotagmin. A complex implicated in synaptic vesicle exocytosis. Journal of Biological Chemistry 1994; 269: 6306–6312
   PubMedGoogle Scholar
• Lew J., Wang J. H. Neuronal cdc2-like kinase. Trends in Biochemical Sciences 1995; 20: 33–37
   PubMedGoogle Scholar
• Lew J., Huang Q. Q., Qi Z., Winkfein R. J., Aebersold R., Hunt T., Wang J. H. A brain-specific activator of cyclin-dependent kinase 5. Nature 1994; 371: 423–426
   PubMed Web of Science ®Google Scholar
• Liang J., Chen J. K., Schreiber S. L., Clardy J. Crystal structure of P13K SH3 domain at 2–0 A resolution. Journal of Molecular Biology 1996; 257: 632–643
   PubMedGoogle Scholar
• Lichte B., Veh R. W., Meyer H. E., Kilimann M. W. Amphiphysin, a novel protein associated with synaptic vesicles. EMBO Journal 1992; 11: 2521–2530
   PubMed Web of Science ®Google Scholar
• Lindner R., Ungewickell E. Clathrin-associated proteins of bovine brain coated vesicles: an analysis of their number and assembly-promoting activity. Journal of Biological Chemistry 1992; 267: 16567–16573
   PubMedGoogle Scholar
• Linial M. Proline clustering in proteins from synaptic vesicles. Neuroreport 1994; 5: 2009–2015
   PubMedGoogle Scholar
• Litchfield D. W., Luscher B., Lozeman F. J., Eisenman R. N., Krebs E. G. Phosphorylation of casein kinase II by p34cdc2 in vitro and at mitosis. Journal of Biological Chemistry 1992; 267: 13943–13951
   PubMed Web of Science ®Google Scholar
• Littleton J. T., Bellen H. J. Synaptotagmin controls and modulates synaptic-vesicle fusion in a Ca2+-dependent manner. Trends in Neuroscience 1995; 18: 177–183
   PubMedGoogle Scholar
• Liu J. P., Robinson P. J. Dynamin and endocytosis. Endocrine Reviews 1995; 16: 590–607
   PubMed Web of Science ®Google Scholar
• Liu J. P., Powell K. A., Sudhof T. C., Robinson P. J. Dynamin I is a Ca2+-sensitive phospholipid-binding protein with very high affinity for protein kinase C. Journal of Biological Chemistry 1994; 269: 21043–21050
   PubMedGoogle Scholar
• Liu J. P., Sim A. T. R., Robinson P. J. Calcineurin inhibition of dynamin I GTPase activity coupled to nerve terminal depolarization. Science 1994; 265: 970–973
   PubMedGoogle Scholar
• Liu J. P., Zhang Q. X., Baldwin G., Robinson P. J. Calcium binds dynamin I and inhibits its GTPase activity. Journal of Neurochemistry 1996; 66: 2074–2081
   PubMedGoogle Scholar
• Maeda K., Nakata T., Noda Y., Sato-Yoshitake R., Hirokawa N. Interaction of dynamin with microtubules: its structure and GTPase activity investigated by using highly purified dynamin. Molecular Biology of the Cell 1992; 3: 1181–1194
   PubMedGoogle Scholar
• Mahadevan D., Thanki N., Singh J., McPhie P., Zangrilli D., Wang L. M., Guerrero C., LeVine H., III, Humblet C., Saldanha J., Gutkind J. S., Najmabadi-Haske T. Structural studies on the PH domains of Dbl, Sos1, IRS-1, and βARK1 and their differential binding to Gβgamma subunits. Biochemistry 1995; 34: 9111–9117
   PubMedGoogle Scholar
• Maier O., Knoblich M., Westermann P. Dynamin II binds to the trans-Golgi network. Biochemical and Biophysical Research Communications 1996; 223: 229–233
   PubMedGoogle Scholar
• Martin K. C., Hu Y. H., Armitage B. A., Siegelbaum S. A., Kandel E. R., Kaang B. K. Evidence for synaptotagmin as an inhibitory clamp on synaptic vesicle release in Aplysia neurons. Proceedings of the National Academy of Sciences, USA 1995; 92: 11307–11311
   PubMedGoogle Scholar
• Matteoli M., Haimann C., Torri-Tarelli F., Polak J. M., Ceccarelli B., Najmabadi-De Camilli P. Differential effect of alpha-latrotoxin on exocytosis from small synaptic vesicles and from large dense-core vesicles containing calcitonin gene-related peptide at the frog neuromuscular junction. Proceedings of the National Academy of Sciences, USA 1988; 85: 7366–7370
   PubMedGoogle Scholar
• Matthews G. Neurotransmitter release. Annual Review of Neuroscience 1996; 19: 219–233
   PubMed Web of Science ®Google Scholar
• Mayer B. J., Ren R., Clark K. L., Baltimore D. A putative modular domain present in diverse signaling proteins. Cell 1993; 73: 629–630
   PubMed Web of Science ®Google Scholar
• McPherson P. S., Takei K., Schmid S. L., De Camilli P. p145, a major Grb2-binding protein in brain, is co-localized with dynamin in nerve terminals where it undergoes activity-dependent dephosphorylation. Journal of Biological Chemistry 1994; 269: 30132–30139
   PubMedGoogle Scholar
• McPherson P. S., Garcia E. P., Slepnev V. I., David C., Zhang X. M., Grabs D., Sossin W. S., Bauerfeind R., Nemoto Y., De Camilli P. A presynaptic inositol-5-phosphatase. Nature 1996; 379: 353–357
   PubMed Web of Science ®Google Scholar
• Miki H., Miura K., Matuoka K., Nakata T., Hirokawa N., Orita S., Kaibuchi K., Takai Y., Takenawa T. Association of Ash/Grb-2 with dynamin through the Src homology 3 domain. Journal of Biological Chemistry 1994; 269: 5489–5492
   PubMedGoogle Scholar
• Miller T. M., Heuser J. E. Endocytosis of synaptic vesicle membrane at the frog neuromuscular junction. Journal of Cell Biology 1984; 98: 685–698
   PubMedGoogle Scholar
• Mochly-Rosen D., Khaner H., Lopez J., Smith B. L. Intracellular receptors for activated protein kinase C. Identification of a binding site for the enzyme. Journal of Biological Chemistry 1991; 266: 14866–14868
   PubMed Web of Science ®Google Scholar
• Monck J. R., Oberhauser A. F., Fernandez J. M. The exocytotic fusion pore interface: a model of the site of neurotransmitter release. Molecular Membrane Biology 1995; 12: 151–156
   PubMed Web of Science ®Google Scholar
• Mulner-Lorillon O., Cormier P., Labbe J. C., Doree M., Poulhe R., Osborne H., Belle R. M-phase-specific cdc2 protein kinase phosphorylates the β subunit of casein kinase II and increases casein kinase II activity. European Journal of Biochemistry 1990; 193: 529–534
   PubMedGoogle Scholar
• Muro Y., Chan E. K., Landberg G., Tan E. M. A cell-cycle nuclear autoantigen containing WD-40 motifs expressed mainly in S and G2 phase cells. Biochemical and Biophysical Research Communications 1995; 207: 1029–1037
   PubMed Web of Science ®Google Scholar
• Musacchio A., Noble M., Pauptit R., Wierenga R., Saraste M. Crystal structure of a Src-homology 3 (SH3) domain. Nature 1992; 359: 851–855
   PubMed Web of Science ®Google Scholar
• Musacchio A., Gibson T., Rice P., Thompson J., Saraste M. The PH domain: a common piece in the structural patchwork of signalling proteins. Trends in Biochemical Sciences 1993; 18: 343–348
   PubMed Web of Science ®Google Scholar
• Nakata T., Takemura R., Hirokawa N. A novel member of the dynamin family of GTP-binding proteins is expressed specifically in the testis. Journal of Cell Science 1993; 105: 1–5
   PubMedGoogle Scholar
• Nakayama M., Yazaki K., Kusano A., Nagata K., Hanai N., Ishihama A. Structure of mouse Mx1 protein. Molecular assembly and GTP-dependent conformational change. Journal of Biological Chemistry 1993; 268: 15033–15038
   PubMedGoogle Scholar
• Neher E. Secretion without full fusion. Nature 1993; 363: 497–498
   PubMedGoogle Scholar
• Newman T., de Bruijn F. J., Green P., Keegstra K., Kende H., McIntosh L., Ohlrogge J., Raikhel N., Somerville S., Thomashow M., Retzel E., Somerville C. Genes galore: a summary of methods for accessing results from large-scale partial sequencing of anonymous Arabidopsis cDNA clones. Plant Physiology 1994; 106: 1241–1255
   PubMedGoogle Scholar
• Newton A. C. Protein kinase C: structure, function, and regulation. Journal of Biological Chemistry 1995; 270: 28495–28498
   PubMed Web of Science ®Google Scholar
• Niemann H., Blasi J., Jahn R. Clostridial neurotoxins: new tools for dissecting exocytosis. Trends in Cell Biology 1994; 4: 179–188
   PubMedGoogle Scholar
• Norris F. A., Ungewickell E., Majerus P. W. Inositol hexakisphosphate binds to clathrin assembly protein 3 (AP-3/AP180) and inhibits clathrin cage assembly in vitro. Journal of Biological Chemistry 1995; 270: 214–217
   PubMed Web of Science ®Google Scholar
• Nuoffer C., Balch W. E. GTPases: multifunctional molecular switches regulating vesicular traffic. Annual Review of Biochemistry 1994; 63: 949–990
   PubMed Web of Science ®Google Scholar
• Obar R. A., Shpetner H. S., Vallee R. B. Dynamin: a microtubule-associated GTP-binding protein. Journal of Cell Science Supplement 1991; 14: 143–145
   PubMedGoogle Scholar
• Okabayashi Y., Sugimoto Y., Totty N. F., Hsuan J., Kido Y., Sakaguchi K., Gout I., Waterfield M. D., Kasuga M. Interaction of Shc with adaptor protein adaptins. Journal of Biological Chemistry 1996; 271: 5265–5269
   PubMed Web of Science ®Google Scholar
• Park D., John D. Y., Lee C. W., Lee K. H., Rhee S. G. Activation of phospholipase C isozymes by G protein beta-gamma subunits. Journal of Biological Chemistry 1993; 268: 4573–4576
   PubMed Web of Science ®Google Scholar
• Parker P. J., Hemmings B. A., Gierschik P. PH domains and phospholipases—a meaningful relationship. Trends in Biochemical Sciences 1994; 19: 54–55
   PubMedGoogle Scholar
• Parsons T. D., Lenzi D., Aimers W., Roberts W. M. Calcium-triggered exocytosis and endocytosis in an isolated presynaptic cell: capacitance measurements in saccular hair cells. Neuron 1994; 13: 875–883
   PubMedGoogle Scholar
• Pavlovic J., Schroder A., Blank A., Pitossi F., Staeheli P. Mx proteins: GTPases involved in the interferon-induced antiviral state. Ciba Foundation Symposiums 1993; 176: 233–243
   PubMedGoogle Scholar
• Pawson T. SH2 and SH3 domains in signal transduction. Advances in Cancer Research 1994; 64: 87–110
   PubMed Web of Science ®Google Scholar
• Pawson T. Protein modules and signalling networks. Nature 1995; 373: 573–580
   PubMed Web of Science ®Google Scholar
• Pearse B. M., Robinson M. S. Clathrin, adaptors, and sorting. Annual Review of Cell Biology 1990; 6: 151–171
   PubMedGoogle Scholar
• Peeler J. S., Donzell W. C., Anderson R. G. The appendage domain of the AP-2 subunit is not required for assembly or invagination of clathrin-coated pits. Journal of Cell Biology 1993; 120: 47–54
   PubMedGoogle Scholar
• Pines J. Cyclins and cyclin-dependent kinases: a biochemical view. Biochemical Journal 1995; 308: 697–711
   PubMed Web of Science ®Google Scholar
• Pitcher J. A., Inglese J., Higgins J. B., Arriza J. L., Casey P. J., Kim C., Benovic J. L., Kwatra M. M., Caron M. G., Lefkowitz R. J. Role of beta-gamma subunits of G proteins in targeting the β-adrenergic receptor kinase to membrane-bound receptors. Science 1992; 257: 1264–1267
   PubMed Web of Science ®Google Scholar
• Pitcher J. A., Touhara K., Payne E. S., Lefkowitz R. J. Pleckstrin homology domain-mediated membrane association and activation of the β-adrenergic receptor kinase requires coordinate interaction with G-beta-gamma subunits and lipid. Journal of Biological Chemistry 1995; 270: 11707–11710
   PubMed Web of Science ®Google Scholar
• Pley U., Parham P. Clathrin: its roles in receptor-mediated vesicular transport and specialised functions in neurons. Critical Reviews in Biochemistry and Molecular Biology 1993; 28: 431–464
   PubMed Web of Science ®Google Scholar
• Ponting C. P., Parker P. J. Extending the C2 domain family: C2s in PKCs δ, sN, eta, PH, phospholipases, GAPs, and perforin. Protein Science 1996; 5: 162–166
   PubMed Web of Science ®Google Scholar
• Poodry C. A., Edgar L. Reversible alterations in the neuromuscular junctions of Drosophila melanogaster bearing a temperature-sensitive mutation, shibire. Journal of Cell Biology 1979; 81: 520–527
   PubMed Web of Science ®Google Scholar
• Powell K. A., Robinson P. J. Dephosphin/dynamin is a neuronal phosphoprotein concentrated in nerve terminals: evidence from rat cerebellum. Neuroscience 1995; 64: 821–833
   PubMedGoogle Scholar
• Pypaert M., Mundy D. I., Souter E., Labbé J. C., Warren G. Mitotic cytosol inhibits invagination of coated pits in broken mitotic cells. Journal of Cell Biology 1991; 114: 1159–1166
   PubMedGoogle Scholar
• Ramaswami M., Krishnan K. S., Kelly R. B. Intermediates in synaptic vesicle recycling revealed by optical imaging of Drosophila neuromuscular junctions. Neuron 1994; 13: 363–375
   PubMed Web of Science ®Google Scholar
• Robinson M. S. The role of clathrin, adaptors and dynamin in endocytosis. Current Opinion in Cell Biology 1994; 6: 538–544
   PubMed Web of Science ®Google Scholar
• Robinson P. J. Characterisation of dephosphin: 96,000 and 93,000 dalton substrates of protein kinase C in rat and human brain synaptosomal cytosol and synaptic vesicles. Neuroscience Research Communications 1991; 9: 167–176
   Google Scholar
• Robinson P. J. Differential stimulation of protein kinase C activity by phorbol ester or calcium/phosphatidylserine in vitro and in intact synaptosomes. Journal of Biological Chemistry 1992; 267: 21637–21644
   PubMedGoogle Scholar
• Robinson P. J., Dunkley P. R. Depolarisation-dependent protein phosphorylation in rat cortical synaptosomes: factors determining the magnitude of the response. Journal of Neurochemistry 1983; 41: 909–918
   PubMedGoogle Scholar
• Robinson P. J., Hauptschein R., Lovenberg W., Dunkley P. R. Dephosphorylation of synaptosomal proteins P96 and P139 is regulated by both depolarization and calcium, but not by a rise in cytosolic calcium alone. Journal of Neurochemistry 1987; 48: 187–195
   PubMed Web of Science ®Google Scholar
• Robinson P. J., Sontag J. M., Liu J. P., Fykse E. M., Slaughter C., McMahon H. T., Südhof T. C. Dynamin GTPase regulated by protein kinase C phosphorylation in nerve terminals. Nature 1993; 365: 163–166
   PubMed Web of Science ®Google Scholar
• Robinson P. J., Liu J. P., Powell K. A., Fykse E. M., Südhof T. C. Phosphorylation of dynamin I and synaptic vesicle recycling. Trends in Neuroscience 1994; 17: 348–353
   PubMedGoogle Scholar
• Ron D., Mochly-Rosen D. Agonists and antagonists of protein kinase C function, derived from its binding proteins. Journal of Biological Chemistry 1994; 269: 21395–21398
   PubMedGoogle Scholar
• Ron D., Chen C. H., Caldwell J., Jamieson L., Orr E., Mochly-Rosen D. Cloning of an intracellular receptor for protein kinase C: A homolog of the β subunit of G proteins. Proceedings of the National Academy of Sciences, USA 1994; 91: 839–843
   PubMed Web of Science ®Google Scholar
• Rothman J. E., Orci L. Molecular dissection of the secretory pathway. Nature 1992; 355: 409–415
   PubMed Web of Science ®Google Scholar
• Rothman J. H., Raymond C. K., Gilbert T., McO'Hara P., Stevens T. A putative GTP binding proteins homologous to interferon-inducible Mx proteins performs an essential function in yeast protein sorting. Cell 1990; 61: 1063–1074
   PubMed Web of Science ®Google Scholar
• Ryan T. A., Smith S. J. Vesicle pool mobilization during action potential firing at hippocampal synapses. Neuron 1995; 14: 983–989
   PubMedGoogle Scholar
• Ryan T. A., Reuter H., Wendland B., Schweizer F. E., Tsien R. W., Smith S. J. The kinetics of synaptic vesicle recycling measured at single presynaptic boutons. Neuron 1993; 11: 713–724
   PubMedGoogle Scholar
• Ryan T. A., Smith S. J., Reuter H. The timing of synaptic vesicle endocytosis. Proceedings of the National Academy of Sciences, USA 1996; 93: 5567–5571
   PubMedGoogle Scholar
• Sandvig K., Van Deurs B. Endocytosis without clathrin. Trends in Cell Biology 1994; 4: 275–277
   PubMedGoogle Scholar
• Saraste M., Hyvönen M. Pleckstrin homology domains: a fact file. Current Opinion in Structural Biology 1995; 5: 403–408
   PubMed Web of Science ®Google Scholar
• Scaife R., Margolis R. L. Biochemical and immunochemical analysis of rat brain dynamin interaction with microtubules and organelles in vivo and in vitro. Journal of Cell Biology 1990; 111: 3023–3033
   PubMedGoogle Scholar
• Scaife R., Gout I., Waterfield M. D., Margolis R. L. Growth factor-induced binding of dynamin to signal transduction proteins involves sorting to distinct and separate proline-rich dynamin sequences. EMBO Journal 1994; 13: 2574–2582
   PubMedGoogle Scholar
• Scheller R. H. Membrane trafficking in the presynaptic nerve terminal. Neuron 1995; 14: 893–897
   PubMedGoogle Scholar
• Schiavo G., Benfenati F., Poulain B., Rossetto O., Polverino deLaureto P., Dasgupta B. R., Montecucco C. Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin. Nature 1992; 359: 832–835
   PubMed Web of Science ®Google Scholar
• Schmid S. L. The mechanism of receptor-mediated endocytosis: more questions than answers. BioEssays 1992; 14: 589–596
   PubMed Web of Science ®Google Scholar
• Schmid S. L. Coated vesicle formation in vitro: conflicting results using different assays. Trends in Cell Biology 1993; 3: 145–148
   PubMedGoogle Scholar
• Schroeder T. J., Borges R., Finnegan J. M., Pihel K., Amatore C., Wightman R. M. Temporally resolved, independent stages of individual exocytotic secretion events. Biophysical Journal 1996; 70: 1061–1068
   PubMedGoogle Scholar
• Schweizer F. E., Betz H., Augustine G. J. From vesicle docking to endocytosis: intermediate reactions of exocytosis. Neuron 1995; 14: 689–696
   PubMed Web of Science ®Google Scholar
• Seedorf K., Kostka G., Lammers R., Bashkin P., Daly R., Burgess W. H., van der Bliek A. M., Schlessinger J., Ullrich A. Dynamin binds to SH3 domains of phospholipase CsG and GRB-2. Journal of Biological Chemistry 1994; 269: 16009–16014
   PubMed Web of Science ®Google Scholar
• Shaw G. Identification of novel pleckstrin homology (PH) domains provides a hypothesis for PH domain function. Biochemical and Biophysical Research Communications 1993; 195: 1145–1151
   PubMedGoogle Scholar
• Shpetner H. S., Vallee R. B. Identification of dynamin, a novel mechanochemical enzyme that mediates interactions between microtubules. Cell 1989; 59: 421–432
   PubMed Web of Science ®Google Scholar
• Shpetner H. S., Vallee R. B. Dynamin is a GTPase stimulated to high levels of activity by microtubules. Nature 1992; 355: 733–735
   PubMedGoogle Scholar
• Shpetner H. S., Herskovits J. S., Vallee R. B. A binding site for SH3 domains targets dynamin to coated pits. Journal of Biological Chemistry 1996; 271: 13–16
   PubMedGoogle Scholar
• Sivadon P., Bauer F., Aigle M., Crouzet M. Actin cytoskeleton and budding pattern are altered in the yeast rvs161 mutant: the Rvs161 protein shares common domains with the brain protein amphiphysin. Molecular and General Genetics 1995; 246: 485–495
   PubMedGoogle Scholar
• Smith C. B., Betz W. J. Simultaneous independent measurement of endocytosis and exocytosis. Nature 1996; 380: 531–534
   PubMed Web of Science ®Google Scholar
• Smythe E., Warren G. The mechanism of receptor-mediated endocytosis. European Journal of Biochemistry 1991; 202: 689–699
   PubMedGoogle Scholar
• Söllner T., Bennett M. K., Whiteheart S. W., Scheller R. H., Rothman J. E. A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion. Cell 1993; 75: 409–418
   PubMed Web of Science ®Google Scholar
• Solomon M. J. Activation of the various cyclin/cdc2 protein kinases. Current Opinion in Cell Biology 1993; 5: 180–186
   PubMed Web of Science ®Google Scholar
• Sontag J. M., Fykse E. M., Ushkaryov Y., Liu J. P., Robinson P. J., Südhof T. C. Differential expression and regulation of multiple dynamins. Journal of Biological Chemistry 1994; 269: 4547–4554
   PubMedGoogle Scholar
• Sorkin A., McKinsey T., Shih W., Kirchhausen T., Carpenter G. Stoichiometric interaction of the epidermal growth factor receptor with the clathrin-associated protein complex AP-2. Journal of Biological Chemistry 1995; 270: 619–625
   PubMedGoogle Scholar
• Sorkin A., Mazzotti M., Sorkina T., Scotto L., Beguinot L. Epidermal growth factor receptor interaction with clathrin adaptors is mediated by the Tyr974-containing internalization motif. Journal of Biological Chemistry 1996; 271: 13377–13384
   PubMedGoogle Scholar
• Stack J. H., Horazdovsky B., Emr S. D. Receptor-mediated protein sorting to the vacuole in yeast: Roles for a protein kinase, a lipid kinase and GTP-binding proteins. Annual Review of Cell Biology 1995; 11: 1–33
   Google Scholar
• Staeheli P., Haller O., Boll W., Lindenmann J., Weissmann C. Mx protein: constitutive expression in 3T3 cells transformed with cloned Mx cDNA confers selective resistance to influenza virus. Cell 1986; 44: 147–158
   PubMed Web of Science ®Google Scholar
• Steinman R. E., Mellman I. S., Muller W. A., Cohn Z. A. Endocytosis and the recycling of plasma membrane. Journal of Cell Biology 1983; 96: 1–27
   PubMed Web of Science ®Google Scholar
• Subtil A., Hémar A., Dautry-Varsat A. Rapid endocytosis of interleukin 2 receptors when clathrin-coated pit endocytosis is inhibited. Journal of Cell Science 1994; 107: 3461–3468
   PubMedGoogle Scholar
• Südhof T. C. The synaptic vesicle cycle: a cascade of protein-protein interactions. Nature 1995; 375: 645–653
   PubMed Web of Science ®Google Scholar
• Swaroop A., Yang Feng T. L., Liu W., Gieser L., Barrow L. L., Chen K. C., Agarwal N., Meisler M. H., Smith D. I. Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6. Human Molecular Genetics 1994; 3: 1281–1286
   PubMedGoogle Scholar
• Takei K., McPherson P. S., Schmid S. L., De Camilli P. Tubular membrane invaginations coated by dynamin rings are induced by GTP-sG-gammaS in nerve terminals. Nature 1995; 374: 186–190
   PubMed Web of Science ®Google Scholar
• Takei K., Mundigl O., Daniell L., De Camilli P. The synaptic vesicle cycle: a single vesicle budding step involving clathrin and dynamin. Journal of Cell Biology 1996; 133: 1237–1250
   PubMedGoogle Scholar
• Terasawa H., Kohda D., Hatanaka H., Tsuchiya S., Ogura K., Nagata K., Ishii S., Mandiyan V., Ullrich A., Schlessinger J., Inagaki F. Structure of the N-terminal SH3 domain of GRB2 complexed with a peptide from the guanine nucleotide releasing factor Sos. Structural Biology 1994; 1: 891–897
   PubMedGoogle Scholar
• Thomas P., Lee A. K., Wong J. G., Almers W. A triggered mechanism retrieves membrane in seconds after Ca2+-stimulated exocytosis in single pituitary cells. Journal of Cell Biology 1994; 124: 667–675
   PubMed Web of Science ®Google Scholar
• Timm D., Salim K., Gout I., Guruprasad L., Waterfield M., Blundell T. Crystal structure of the pleckstrin homology domain from dynamin. Nature Structural Biology 1995; 1: 782–788
   Google Scholar
• Toker A., Ellis C. A., Sellers L. A., Aitken A. Protein kinase C inhibitor proteins-Purification from sheep brain and sequence similarity to lipocortins and 14–3–3 protein. European Journal of Biochemistry 1990; 191: 421–429
   PubMedGoogle Scholar
• Torri-Tarelli F., Haimann C., Ceccarelli B. Coated vesicles and pits during enhanced quantal release of acetylcholine at the neuromuscular junction. Journal of Neurocytology 1987; 16: 205–214
   PubMedGoogle Scholar
• Touhara K., Inglese J., Pitcher J. A., Shaw G., Lefkowitz R. J. Binding of G protein beta-gamma subunits to pleckstrin homology domains. Journal of Biological Chemistry 1994; 269: 10217–10220
   PubMedGoogle Scholar
• Touhara K., Koch W. J., Hawes B. E., Lefkowitz R. J. Mutational analysis of the pleckstrin homology domain of the β-adrenergic receptor kinase. Differential effects on Gβgamma and phosphatidylinositol 4,5-bisphosphate binding. Journal of Biological Chemistry 1995; 270: 17000–17005
   PubMedGoogle Scholar
• Trifaró J. M., Vitale M. L. Cytoskeleton dynamics during neurotransmitter release. Trends in Neuroscience 1993; 16: 466–472
   PubMedGoogle Scholar
• Trowbridge I. S. Dynamin, SH3 domains and endocytosis. Current Biology 1993; 3: 773–775
   PubMedGoogle Scholar
• Trowbridge I. S., Collawn J. F., Hopkins C. R. Signal-dependent membrane protein trafficking in the endocytic pathway. Annual Review of Cell Biology 1993; 9: 129–161
   PubMedGoogle Scholar
• Tsai L. H., Delalle I., Caviness V. S., Jr, Chae T., Harlow E. p35 is a neural-specific regulatory subunit of cyclin-dependent kinase 5. Nature 1994; 371: 419–423
   PubMed Web of Science ®Google Scholar
• Tsukada S., Simon M. I., Witte O. N., Katz A. Binding of βsG subunits of heterotrimeric G proteins to the PH domain of Bruton tyrosine kinase. Proceedings of the National Academy of Sciences, USA 1994; 91: 11256–11260
   PubMed Web of Science ®Google Scholar
• Tuma P. L., Collins C. A. Activation of dynamin GTPase is a result of positive cooperativity. Journal of Biological Chemistry 1994; 269: 30842–30847
   PubMedGoogle Scholar
• Tuma P. L., Collins C. A. Dynamin forms polymeric complexes in the presence of lipid vesicles. Characterization of chemically cross-linked dynamin molecules. Journal of Biological Chemistry 1995; 270: 26707–26714
   PubMedGoogle Scholar
• Tuma P. L., Stachniak M. C., Collins C. A. Activation of dynamin GTPase by acidic phospholipids and endogenous rat brain vesicles. Journal of Biological Chemistry 1993; 268: 17240–17246
   PubMedGoogle Scholar
• Ungewickell E., Ungewickell H., Holstein S. E. H., Lindner R., Prasad K., Barouch W., Martin B., Greene L. E., Eisenberg E. Role of auxilin in uncoating clathrin-coated vesicles. Nature 1995; 378: 632–635
   PubMed Web of Science ®Google Scholar
• Vallee R. B., Okamoto P. M. The regulation of endocytosis: identifying dynamin's binding partners. Trends in Cell Biology 1995; 5: 43–47
   PubMedGoogle Scholar
• Valtorta F., Benfenati F., Greengard P. Structure and function of the synapsins. Journal of Biological Chemistry 1992; 267: 7195–7198
   PubMedGoogle Scholar
• Van DeGoor J., Ramaswami M., Kelly R. B. Redistribution of synaptic vesicles and their proteins in temperature-sensitive shibirets1 mutant Drosophila. Proceedings of the National Academy of Sciences, USA 1995; 92: 5739, 5743
   PubMedGoogle Scholar
• van derBliek A. M., Meyerowitz E. M. Dynamin-like protein encoded by the Drosophila shibire gene associated with vesicular traffic. Nature 1991; 351: 411–414
   PubMedGoogle Scholar
• van derBliek A. M., Redelmeier T. E., Damke H., Tisdale E. J., Meyerowitz E. M., Schmid S. L. Mutations in human dynamin block an intermediate stage in coated vesicle formation. Journal of Cell Biology 1993; 122: 553–563
   PubMedGoogle Scholar
• Van derVoorn L., Ploegh H. L. The WD-40 repeat. FEBS Letters 1992; 307: 131–134
   PubMedGoogle Scholar
• Van Deurs B., Peterson O. W., Olsnes S., Sandvig K. The ways of endocytosis. International Review of Cytology 1989; 117: 131–177
   PubMed Web of Science ®Google Scholar
• Vater C. A., Raymond C. K., Ekena K., Howald-Stevenson I., Stevens T. H. The VPS1 protein, a homolog of dynamin required for vacuolar protein sorting in Saccharomyces cerevisiae, is a GTPase with two functionally separable domains. Journal of Cell Biology 1992; 119: 773–786
   PubMed Web of Science ®Google Scholar
• Volknandt W. The synaptic vesicle and its targets. Neuroscience 1995; 64: 277–300
   PubMed Web of Science ®Google Scholar
• Von Gersdorff H., Matthews G. Inhibition of endocytosis by elevated internal calcium in a synaptic terminal. Nature 1994; 370: 652–655
   PubMedGoogle Scholar
• Von Gersdorff H., Matthews G. Dynamics of synaptic vesicle fusion and membrane retrieval in synaptic terminals. Nature 1994; 367: 735–739
   PubMed Web of Science ®Google Scholar
• Von Grafenstein H., Knight D. E. Triggered exocytosis and endocytosis have different requirements for calcium and nucleotides in permeabilized bovine chromaffin cells. Journal of Membrane Biology 1993; 134: 1–13
   PubMedGoogle Scholar
• Von Grafenstein H., Roberts C. S., Baker P. F. Kinetic analysis of the triggered exocytosis/endocytosis secretory cycle in cultured bovine adrenal medullary cells. Journal of Cell Biology 1986; 103: 2343–2352
   PubMedGoogle Scholar
• Wang D. S., Shaw R., Winkelmann J. C., Shaw G. Binding of PH domains of β-adrenergic receptor kinase and β-spectrin to WD40/β-transducin repeat containing regions of the β-subunit of trimeric G-proteins. Biochemical and Biophysical Research Communications 1994; 203: 29–35
   PubMed Web of Science ®Google Scholar
• Wang D. S., Shaw R., Hattori M., Arai H., Inoue K., Shaw G. Binding of pleckstrin homology domains to WD40/β-transducin repeat containing segments of the protein product of the Lis-1 gene. Biochemical and Biophysical Research Communications 1995; 209: 622–629
   PubMedGoogle Scholar
• Wang L. H., Rothberg K. G., Anderson R. G. Misassembly of clathrin lattices on endosomes reveals a regulatory switch for coated pit formation. Journal of Cell Biology 1993; 123: 1107–1117
   PubMed Web of Science ®Google Scholar
• Wang L. H., Südhof T. C., Anderson R. G. The appendage domain of aP-adaptin is a high affinity binding site for dynamin. Journal of Biological Chemistry 1995; 270: 10079–10083
   PubMedGoogle Scholar
• Wang Z. X., Moran M. F. Requirement for the adapter protein GRB2 in EGF receptor endocytosis. Science 1996; 272: 1935–1939
   PubMed Web of Science ®Google Scholar
• Warnock D. E., Terlecky L. J., Schmid S. L. Dynamin GTPase is stimulated by crosslinking through the C-terminal proline-rich domain. EMBO Journal 1995; 14: 1322–1328
   PubMedGoogle Scholar
• Warnock D. E., Hinshaw J. E., Schmid S. L. Dynamin self-assembly stimulates its GTPase activity. Journal of Biological Chemistry 1996; 271: 22310–22314
   PubMedGoogle Scholar
• Whiteheart S. W., Kubalek E. W. SNAPs and NSF: General members of the fusion apparatus. Trends in Cell Biology 1995; 5: 64–68
   PubMedGoogle Scholar
• Williamson M. P. The structure and function of proline-rich regions in proteins. Biochemical Journal 1994; 297: 249–260
   PubMed Web of Science ®Google Scholar
• Woodman P. G., Adamczewski J. P., Hunt T., Warren G. In vitro fusion of endocytic vesicles is inhibited by cyclin A-cdc2 kinase. Molecular Biology, Cell 1993; 4: 541–553
   PubMedGoogle Scholar
• Yao L., Kawakami Y., Kawakami T. The pleckstrin homology domain of Bruton tyrosine kinase interacts with protein kinase C. Proceedings of the National Academy of Sciences, USA 1994; 91: 9175–9179
   PubMed Web of Science ®Google Scholar
• Ye W., Ali N., Bembenek M. E., Shears S. B., Lafer E. M. Inhibition of clathrin assembly by high affinity binding of specific inositol polyphosphates to the synapse-specific clathrin assembly protein AP-3. Journal of Biological Chemistry 1995; 270: 1564–1568
   PubMed Web of Science ®Google Scholar
• Yu H., Rosen M. K., Shin T. B., Seidel-Dugan C., Brugge J. S., Schreiber S. L. Solution structure of the SH3 domain of Src and identification of its ligand-binding site. Science 1992; 258: 1665–1668
   PubMed Web of Science ®Google Scholar
• Zhang J., Ferguson S. G., Barak L. S., Menard L., Caron M. G. Dynamin and β-arrestin reveal distinct mechanisms for G protein-coupled receptor internalization. Journal of Biological Chemistry 1996; 271: 18302–18305
   PubMed Web of Science ®Google Scholar
• Zhang J. Z., Davletov B. A., Südhof T. C., Anderson R. G. Synaptotagmin I is a high affinity receptor for clathrin AP-2: Implications for membrane recycling. Cell 1994; 78: 751–760
   PubMedGoogle Scholar
• Zheng J., Cahill S. M., Lemmons M. A., Fushman D., Schlessinger J., Cowburn D. Identification of the binding site for acidic phospholipids on the PH domains of dynamin: implications for stimulation of GTPase activity. Journal of Molecular Biology 1996; 255: 14–21
   PubMedGoogle Scholar