Reconstitution of regulated exocytosis in cell-free systems: a critical appraisal.

Regulated exocytosis involves the tightly controlled fusion of a transport vesicle with the plasma membrane. It includes processes as diverse as the release of neurotransmitters from presynaptic nerve endings and the sperm-triggered deposition of a barrier preventing polyspermy in oocytes. Cell-free model systems have been developed for studying the biochemical events underlying exocytosis. They range from semi-intact permeabilized cells to the reconstitution of membrane fusion from isolated secretory vesicles and their target plasma membranes. Interest in such cell-free systems has recently been reinvigorated by new evidence suggesting that membrane fusion is mediated by a basic mechanism common to all intracellular fusion events. In this chapter, we review some of the literature in the light of these new developments and attempt to provide a critical discussion of the strengths and limitations of the various cell-free systems.

[1]  G. Matthews,et al.  Electrophysiology of synaptic vesicle cycling. , 1999, Annual review of physiology.

[2]  T. Südhof,et al.  Genetics of synaptic vesicle function: toward the complete functional anatomy of an organelle. , 1999, Annual review of physiology.

[3]  J. Edwardson A cell-free system for Ca2+-regulated exocytosis. , 1998, Methods.

[4]  D. Aunis,et al.  Identification of a Potential Effector Pathway for the Trimeric Go Protein Associated with Secretory Granules , 1998, The Journal of Biological Chemistry.

[5]  P. Hanson,et al.  Membrane fusion: SNAREs line up in new environment , 1998, Nature.

[6]  R. Scheller,et al.  Seven Novel Mammalian SNARE Proteins Localize to Distinct Membrane Compartments* , 1998, The Journal of Biological Chemistry.

[7]  P. Padfield,et al.  The two phases of regulated exocytosis in permeabilized pancreatic acini are modulated differently by heterotrimeric G-proteins. , 1998, Biochemical and biophysical research communications.

[8]  P. Bronk,et al.  The Pathway of Membrane Fusion Catalyzed by Influenza Hemagglutinin: Restriction of Lipids, Hemifusion, and Lipidic Fusion Pore Formation , 1998, The Journal of cell biology.

[9]  Benedikt Westermann,et al.  SNAREpins: Minimal Machinery for Membrane Fusion , 1998, Cell.

[10]  E. Neher Vesicle Pools and Ca2+ Microdomains: New Tools for Understanding Their Roles in Neurotransmitter Release , 1998, Neuron.

[11]  C. Wollheim,et al.  Ca2+‐independent insulin exocytosis induced by α‐latrotoxin requires latrophilin, a G protein‐coupled receptor , 1998, The EMBO journal.

[12]  D. Aunis,et al.  Regulated Exocytosis in Chromaffin Cells , 1998, The Journal of Biological Chemistry.

[13]  T. Südhof,et al.  RAB3 and synaptotagmin: the yin and yang of synaptic membrane fusion. , 1998, Annual review of neuroscience.

[14]  P. Halban,et al.  SNAP-23 Is Not Cleaved by Botulinum Neurotoxin E and Can Replace SNAP-25 in the Process of Insulin Secretion* , 1997, The Journal of Biological Chemistry.

[15]  Hui Zhang,et al.  Transient expression of botulinum neurotoxin C1 light chain differentially inhibits calcium and glucose induced insulin secretion in clonal β‐cells , 1997, FEBS letters.

[16]  M. Götte,et al.  Vesicular transport: how many Ypt/Rab-GTPases make a eukaryotic cell? , 1997, Trends in biochemical sciences.

[17]  H. Pelham EJCB-Lecture. SNAREs and the organization of the secretory pathway. , 1997, European journal of cell biology.

[18]  M. Poo,et al.  Overexpression of synaptotagmin modulates short-term synaptic plasticity at developing neuromuscular junctions , 1997, Neuroscience.

[19]  H. Horvitz,et al.  Caenorhabditis elegans rab-3 Mutant Synapses Exhibit Impaired Function and Are Partially Depleted of Vesicles , 1997, The Journal of Neuroscience.

[20]  K. Howell,et al.  Phosphatidylinositol 3–Kinase Is Required for the Formation of Constitutive Transport Vesicles from the TGN , 1997, The Journal of cell biology.

[21]  R. Scheller,et al.  Better Late Than Never: A Role for Rabs Late in Exocytosis , 1997, Neuron.

[22]  Guo-Qiang Bi,et al.  Kinesin- and Myosin-driven Steps of Vesicle Recruitment for Ca2+-regulated Exocytosis , 1997, The Journal of cell biology.

[23]  S. Conner,et al.  Members of the SNARE hypothesis are associated with cortical granule exocytosis in the sea urchin egg , 1997, Molecular reproduction and development.

[24]  K. Loyet,et al.  Novel Ca2+-binding Protein (CAPS) Related to UNC-31 Required for Ca2+-activated Exocytosis* , 1997, The Journal of Biological Chemistry.

[25]  Thomas C. Südhof,et al.  Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion , 1997, Nature.

[26]  M. Zerial,et al.  The diversity of Rab proteins in vesicle transport. , 1997, Current opinion in cell biology.

[27]  R. Jahn,et al.  The Secretory Granule Protein Syncollin Binds to Syntaxin in a Ca2+-Sensitive Manner , 1997, Cell.

[28]  M. Whitaker,et al.  In vitro exocytosis in sea urchin eggs requires a synaptobrevin-related protein. , 1997, Journal of cell science.

[29]  M. C. Pedroso de Lima,et al.  Evidence that synaptobrevin is involved in fusion between synaptic vesicles and synaptic plasma membrane vesicles. , 1997, Biochemical and biophysical research communications.

[30]  John A. Williams,et al.  Heterotrimeric G-protein Gq/11 Localized on Pancreatic Zymogen Granules Is Involved in Calcium-regulated Amylase Secretion* , 1997, The Journal of Biological Chemistry.

[31]  T. Südhof,et al.  The small GTP-binding protein Rab3A regulates a late step in synaptic vesicle fusion , 1997, Nature.

[32]  P. Hanson,et al.  Neurotransmitter release — four years of SNARE complexes , 1997, Current Opinion in Neurobiology.

[33]  T. Martin Phosphoinositides as spatial regulators of membrane traffic , 1997, Current Opinion in Neurobiology.

[34]  T. Martin,et al.  Docked Secretory Vesicles Undergo Ca2+-activated Exocytosis in a Cell-free System* , 1997, The Journal of Biological Chemistry.

[35]  R. Scheller,et al.  A fusion of new ideas , 1997, Nature.

[36]  J. Helms,et al.  Regulated Exocytosis in Chromaffin Cells , 1997, The Journal of Biological Chemistry.

[37]  A. Mayer,et al.  Docking of Yeast Vacuoles Is Catalyzed by the Ras-like GTPase Ypt7p after Symmetric Priming by Sec18p (NSF) , 1997, The Journal of cell biology.

[38]  V. Olkkonen,et al.  Role of Rab GTPases in membrane traffic. , 1997, International review of cytology.

[39]  M. Bennett,et al.  Distinct cellular locations of the syntaxin family of proteins in rat pancreatic acinar cells. , 1996, Molecular biology of the cell.

[40]  J. Henry,et al.  Evidence for a functional link between Rab3 and the SNARE complex. , 1996, Journal of cell science.

[41]  Subhas Banerjee,et al.  Apobec-1 Interacts with a 65-kDa Complementing Protein to Edit Apolipoprotein-B mRNA in Vitro * , 1996, The Journal of Biological Chemistry.

[42]  C. Dessauer,et al.  Visualizing signal transduction: receptors, G-proteins, and adenylate cyclases. , 1996, Clinical science.

[43]  J A Crowell,et al.  A genetic selection for Caenorhabditis elegans synaptic transmission mutants. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[44]  B. Dasgupta,et al.  N-Ethylmaleimide-sensitive Factor Acts at a Prefusion ATP-dependent Step in Ca2+-activated Exocytosis* , 1996, The Journal of Biological Chemistry.

[45]  B. Dasgupta,et al.  SNAP-25 Is Required for a Late Postdocking Step in Ca2+-dependent Exocytosis* , 1996, The Journal of Biological Chemistry.

[46]  J. Pevsner The role of Sec1p‐related proteins in vesicle trafficking in the nerve terminal , 1996, Journal of neuroscience research.

[47]  Steven S. Vogel,et al.  Poisson-distributed active fusion complexes underlie the control of the rate and extent of exocytosis by calcium , 1996, The Journal of cell biology.

[48]  D. Aunis,et al.  Trimeric G Proteins Control Regulated Exocytosis in Bovine Chromaffin Cells: Sequential Involvement of Go Associated With Secretory Granules and Gi3 Bound to the Plasma Membrane , 1996, The European journal of neuroscience.

[49]  R. Burgoyne,et al.  Botulinum neurotoxin light chains inhibit both Ca2+‐induced and GTP analogue‐induced catecholamine release from permeabilised adrenal chromaffin cells , 1996, FEBS letters.

[50]  J. Valentijn,et al.  Rab3D localizes to secretory granules in rat pancreatic acinar cells. , 1996, European journal of cell biology.

[51]  A. Mayer,et al.  Sec18p (NSF)-Driven Release of Sec17p (α-SNAP) Can Precede Docking and Fusion of Yeast Vacuoles , 1996, Cell.

[52]  J. H. Chou,et al.  Rab3 reversibly recruits rabphilin to synaptic vesicles by a mechanism analogous to raf recruitment by ras. , 1996, The EMBO journal.

[53]  P. De Camilli,et al.  Phosphoinositides as Regulators in Membrane Traffic , 1996, Science.

[54]  R. Scheller,et al.  VAMP/synaptobrevin isoforms 1 and 2 are widely and differentially expressed in nonneuronal tissues , 1996, The Journal of cell biology.

[55]  E. Kandel,et al.  Evidence for synaptotagmin as an inhibitory clamp on synaptic vesicle release in Aplysia neurons. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[56]  H. Horstmann,et al.  Docked granules, the exocytic burst, and the need for ATP hydrolysis in endocrine cells , 1995, Neuron.

[57]  R. Burgoyne,et al.  Stimulation of catecholamine secretion from adrenal chromaffin cells by 14‐3‐3 proteins is due to reorganisation of the cortical actin network , 1995, FEBS letters.

[58]  K. Wirtz,et al.  A role for phosphatidylinositol transfer protein in secretory vesicle formation , 1995, Nature.

[59]  P. Hanson,et al.  Ca2+ Regulates the Interaction between Synaptotagmin and Syntaxin 1 (*) , 1995, The Journal of Biological Chemistry.

[60]  R. Burgoyne,et al.  Distinct effects of alpha-SNAP, 14-3-3 proteins, and calmodulin on priming and triggering of regulated exocytosis , 1995, The Journal of cell biology.

[61]  I. Nishimoto,et al.  Direct control of exocytosis by receptor‐mediated activation of the heterotrimeric GTPases Gi and G(o) or by the expression of their active G alpha subunits. , 1995, The EMBO journal.

[62]  Thomas C. Südhof,et al.  The synaptic vesicle cycle: a cascade of protein–protein interactions , 1995, Nature.

[63]  Thomas C. Südhof,et al.  Ca2+-dependent and -independent activities of neural and non-neural synaptotagmins , 1995, Nature.

[64]  B. Thorens,et al.  VAMP‐2 and cellubrevin are expressed in pancreatic beta‐cells and are essential for Ca(2+)‐but not for GTP gamma S‐induced insulin secretion. , 1995, The EMBO journal.

[65]  B. Wolf,et al.  The Heterotrimeric G-protein Gi Is Localized to the Insulin Secretory Granules of β-Cells and Is Involved in Insulin Exocytosis (*) , 1995, The Journal of Biological Chemistry.

[66]  E. Ikonen,et al.  Different requirements for NSF, SNAP, and Rab proteins in apical and basolateral transport in MDCK cells , 1995, Cell.

[67]  G. Ahnert-Hilger,et al.  Molecular aspects of tetanus and botulinum neurotoxin poisoning , 1995, Progress in Neurobiology.

[68]  S. Nauenburg,et al.  Disassembly of the reconstituted synaptic vesicle membrane fusion complex in vitro. , 1995, The EMBO journal.

[69]  T. Takenawa,et al.  ATP-dependent inositide phosphorylation required for Ca2+-activated secretion , 1995, Nature.

[70]  R. Jahn,et al.  The t-SNAREs syntaxin 1 and SNAP-25 are present on organelles that participate in synaptic vesicle recycling , 1995, The Journal of cell biology.

[71]  S. Muallem,et al.  Actin filament disassembly is a sufficient final trigger for exocytosis in nonexcitable cells , 1995, The Journal of cell biology.

[72]  J. Vincent,et al.  Rab3 proteins: key players in the control of exocytosis , 1994, Trends in Neurosciences.

[73]  S. Emr,et al.  Vps34p required for yeast vacuolar protein sorting is a multiple specificity kinase that exhibits both protein kinase and phosphatidylinositol-specific PI 3-kinase activities. , 1994, The Journal of biological chemistry.

[74]  J. Hsuan,et al.  Identification and partial sequence analysis of novel annexins in Lytechinus pictus oocytes. , 1994, The Biochemical journal.

[75]  P. Weidman,et al.  The G protein-activating peptide, mastoparan, and the synthetic NH2- terminal ARF peptide, ARFp13, inhibit in vitro Golgi transport by irreversibly damaging membranes , 1994, The Journal of cell biology.

[76]  T. Südhof,et al.  Synaptotagmin I: A major Ca2+ sensor for transmitter release at a central synapse , 1994, Cell.

[77]  T. Südhof,et al.  Ca(2+)-dependent conformational change in synaptotagmin I. , 1994, The Journal of biological chemistry.

[78]  P. Brennwald,et al.  Sec9 is a SNAP-25-like component of a yeast SNARE complex that may be the effector of Sec4 function in exocytosis , 1994, Cell.

[79]  R. Jahn,et al.  GTP cleavage by the small GTP-binding protein Rab3A is associated with exocytosis of synaptic vesicles induced by alpha-latrotoxin. , 1994, The Journal of biological chemistry.

[80]  J. Rothman,et al.  A rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles , 1994, Cell.

[81]  B. Wiedenmann,et al.  Requirements for Exocytosis in Permeabilized Neuroendocrine Cells , 1994, Annals of the New York Academy of Sciences.

[82]  T. Kuwana,et al.  Lysosomes can fuse with a late endosomal compartment in a cell-free system from rat liver , 1994, The Journal of cell biology.

[83]  S. Pfeffer Rab GTPases: master regulators of membrane trafficking. , 1994, Current opinion in cell biology.

[84]  Reinhard Jahn,et al.  Vesicle fusion from yeast to man , 1994, Nature.

[85]  W. Wickner,et al.  G-protein ligands inhibit in vitro reactions of vacuole inheritance , 1994, The Journal of cell biology.

[86]  J. Foskett,et al.  Tetanus toxin light chain cleaves a vesicle-associated membrane protein (VAMP) isoform 2 in rat pancreatic zymogen granules and inhibits enzyme secretion. , 1994, The Journal of biological chemistry.

[87]  Thomas C. Südhof,et al.  The role of Rab3A in neurotransmitter release , 1994, Nature.

[88]  R. Jahn,et al.  Clostridial neurotoxins: new tools for dissecting exocytosis. , 1994, Trends in cell biology.

[89]  J. Vincent,et al.  The GTPase Rab3a negatively controls calcium‐dependent exocytosis in neuroendocrine cells. , 1994, The EMBO journal.

[90]  R. Burgoyne,et al.  Control of exocytosis in adrenal chromaffin cells by GTP-binding proteins studied using permeabilized cells and patch-clamp capacitance measurements. , 1994, Biochemical Society transactions.

[91]  S. Seino,et al.  Synaptotagmin III is a novel isoform of rat synaptotagmin expressed in endocrine and neuronal cells. , 1994, The Journal of biological chemistry.

[92]  T. Südhof,et al.  Rab3C is a synaptic vesicle protein that dissociates from synaptic vesicles after stimulation of exocytosis. , 1994, The Journal of biological chemistry.

[93]  T. Südhof,et al.  Rab proteins in regulated exocytosis. , 1994, Trends in biochemical sciences.

[94]  J. Edwardson,et al.  Pancreatic plasma membranes: promiscuous partners in membrane fusion. , 1994, The Biochemical journal.

[95]  A. Pizzey,et al.  The Exocytotic Reaction of Permeabilized Rat Mast Cells , 1994, Annals of the New York Academy of Sciences.

[96]  J. Rothman,et al.  Implications of the SNARE hypothesis for intracellular membrane topology and dynamics , 1994, Current Biology.

[97]  H. V. Gersdorff,et al.  Dynamics of synaptic vesicle fusion and membrane retrieval in synaptic terminals , 1994, Nature.

[98]  S. Wong,et al.  Identification of a vesicle-associated membrane protein (VAMP)-like membrane protein in zymogen granules of the rat exocrine pancreas. , 1994, The Journal of biological chemistry.

[99]  G. Bi,et al.  Cell membrane resealing by a vesicular mechanism similar to neurotransmitter release. , 1994, Science.

[100]  W. Balch,et al.  GTPases: multifunctional molecular switches regulating vesicular traffic. , 1994, Annual review of biochemistry.

[101]  T. Südhof,et al.  A single C2 domain from synaptotagmin I is sufficient for high affinity Ca2+/phospholipid binding. , 1993, The Journal of biological chemistry.

[102]  J. Hay,et al.  Phosphatidylinositol transfer protein required for ATP-dependent priming of Ca2+-activated secretion , 1993, Nature.

[103]  M. Aridor,et al.  Activation of exocytosis by the heterotrimeric G protein Gi3. , 1993, Science.

[104]  Mark K. Bennett,et al.  A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion , 1993, Cell.

[105]  M. Zerial,et al.  Rab proteins and the road maps for intracellular transport , 1993, Neuron.

[106]  J. L. Nieva,et al.  Evaluation of viral membrane fusion assays. Comparison of the octadecylrhodamine dequenching assay with the pyrene excimer assay. , 1993, Biochemistry.

[107]  A. Tsugita,et al.  A complex of rab3A, SNAP‐25, VAMP/synaptobrevin‐2 and syntaxins in brain presynaptic terminals , 1993, FEBS letters.

[108]  J. Edwardson,et al.  Stimulation of exocytotic membrane fusion by modified peptides of the rab3 effector domain: re-evaluation of the role of rab3 in regulated exocytosis. , 1993, The Biochemical journal.

[109]  G. Augustine,et al.  Inhibition of neurotransmitter release by C2-domain peptides implicates synaptotagmin in exocytosis , 1993, Nature.

[110]  K. Takegawa,et al.  Phosphatidylinositol 3-kinase encoded by yeast VPS34 gene essential for protein sorting. , 1993, Science.

[111]  R. Scheller,et al.  The molecular machinery for secretion is conserved from yeast to neurons. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[112]  Paul Tempst,et al.  SNAP receptors implicated in vesicle targeting and fusion , 1993, Nature.

[113]  Steven S. Vogel,et al.  Lysolipids reversibly inhibit Ca2+‐, GTP‐ and pH‐dependent fusion of biological membranes , 1993, FEBS letters.

[114]  R. Zucker,et al.  Multiple calcium-dependent processes related to secretion in bovine chromaffin cells , 1993, Neuron.

[115]  J. Coorssen,et al.  GTPγS and phorbol ester act synergistically to stimulate both Ca2+‐independent secretion and phospholipase D activity in permeabilized human platelets , 1993, FEBS letters.

[116]  R. Scheller,et al.  A role for synaptotagmin (p65) in regulated exocytosis , 1993, Cell.

[117]  P. Novick,et al.  The role of GTP-binding proteins in transport along the exocytic pathway. , 1993, Annual review of cell biology.

[118]  Steven S. Vogel,et al.  Calcium-triggered fusion of exocytotic granules requires proteins in only one membrane. , 1992, The Journal of biological chemistry.

[119]  K. Mostov,et al.  Role of heterotrimeric G proteins in membrane traffic. , 1992, Molecular biology of the cell.

[120]  A. Aitken,et al.  14-3-3 proteins : a highly conserved widespread family of eukaryotic proteins , 2003 .

[121]  S. Ferro-Novick,et al.  Bos1p, a membrane protein required for ER to Golgi transport in yeast, co‐purifies with the carrier vesicles and with Bet1p and the ER membrane. , 1992, The EMBO journal.

[122]  J. Hay,et al.  Resolution of regulated secretion into sequential MgATP-dependent and calcium-dependent stages mediated by distinct cytosolic proteins , 1992, The Journal of cell biology.

[123]  J. Edwardson,et al.  Fusion between rat pancreatic zymogen granules and plasma membranes. Modulation by a GTP-binding protein. , 1992, The Biochemical journal.

[124]  T. Martin,et al.  A novel 145 kd brain cytosolic protein reconstitutes Ca2+-regulated secretion in permeable neuroendocrine cells , 1992, Cell.

[125]  W. Balch,et al.  Synthetic peptides of the effector‐binding domain of rab enhance secretion from digitonin‐permeabilized chromaffin cells , 1992, FEBS letters.

[126]  R. Holz,et al.  Kinetic analysis of secretion from permeabilized adrenal chromaffin cells reveals distinct components. , 1992, The Journal of biological chemistry.

[127]  J. Gruenberg,et al.  Regulation of intracellular membrane transport. , 1992, Current opinion in cell biology.

[128]  N. Sugimoto,et al.  Calmodulin is involved in catecholamine secretion from digitonin-permeabilized bovine adrenal medullary chromaffin cells. , 1992, Biochemical and biophysical research communications.

[129]  H. Sasaki,et al.  A protein factor extracted from murine brains confers physiological Ca2+ sensitivity to exocytosis in sea urchin eggs , 1992, FEBS letters.

[130]  G. Ahnert-Hilger,et al.  Exocytosis from permeabilized bovine adrenal chromaffin cells is differently modulated by guanosine 5'-[gamma-thio]triphosphate and guanosine 5'-[beta gamma-imido]triphosphate. Evidence for the involvement of various guanine nucleotide-binding proteins. , 1992, The Biochemical journal.

[131]  T. Südhof,et al.  Synaptotagmin: a calcium sensor on the synaptic vesicle surface. , 1992, Science.

[132]  B. Gomperts,et al.  Nucleotides and divalent cations as effectors and modulators of exocytosis in permeabilized rat mast cells. , 1992, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[133]  W. Balch,et al.  A synthetic peptide of the rab3a effector domain stimulates amylase release from permeabilized pancreatic acini. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[134]  R. Burgoyne,et al.  Exol and Exo2 proteins stimulate calcium-dependent exocytosis in permeabilized adrenal chromaff in cells , 1992, Nature.

[135]  B. Gomperts,et al.  Regulated exocytotic secretion from permeabilized cells. , 1992, Methods in enzymology.

[136]  D. Aunis,et al.  The participation of annexin II (calpactin I) in calcium-evoked exocytosis requires protein kinase C , 1991, The Journal of cell biology.

[137]  R. Burgoyne Control of exocytosis in adrenal chromaffin cells. , 1991, Biochimica et biophysica acta.

[138]  A. Cleves,et al.  Phospholipid transfer proteins: a biological debut. , 1991, Trends in cell biology.

[139]  T. Whalley,et al.  Phosphoprotein inhibition of calcium-stimulated exocytosis in sea urchin eggs , 1991, The Journal of cell biology.

[140]  D. Aunis,et al.  A pertussis-toxin-sensitive protein controls exocytosis in chromaffin cells at a step distal to the generation of second messengers. , 1991, The Biochemical journal.

[141]  D. Gallwitz,et al.  Identification and structure of four yeast genes (SLY) that are able to suppress the functional loss of YPT1, a member of the RAS superfamily , 1991, Molecular and cellular biology.

[142]  B. Gomperts,et al.  Rat mast cells degranulate in response to microinjection of guanine nucleotide. , 1991, Journal of cell science.

[143]  P. Padfield,et al.  Low molecular weight GTP-binding proteins associated with zymogen granule membranes from rat pancreas. , 1991, Biochemical and biophysical research communications.

[144]  T. Südhof,et al.  A small GTP-binding protein dissociates from synaptic vesicles during exocytosis , 1991, Nature.

[145]  R. Burgoyne,et al.  Evidence for a role of calpactin in calcium-dependent exocytosis. , 1990, Biochemical Society transactions.

[146]  H. Schulman,et al.  Multifunctional Ca2+/calmodulin-dependent protein kinase is necessary for nuclear envelope breakdown , 1990, The Journal of cell biology.

[147]  A. Cleves,et al.  An essential role for a phospholipid transfer protein in yeast Golgi function , 1990, Nature.

[148]  Fusion of neurotransmitter vesicles with target membrane is calcium independent in a cell-free system. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[149]  R. D. De Lisle,et al.  Amylase release from streptolysin O-permeabilized pancreatic acini. , 1990, The American journal of physiology.

[150]  R. Burgoyne,et al.  Stimulation of Ca2(+)-independent catecholamine secretion from digitonin-permeabilized bovine adrenal chromaffin cells by guanine nucleotide analogues. Relationship to arachidonate release. , 1990, The Biochemical journal.

[151]  S. Ferro-Novick,et al.  BET1, BOS1, and SEC22 are members of a group of interacting yeast genes required for transport from the endoplasmic reticulum to the Golgi complex , 1990, Molecular and cellular biology.

[152]  J. Edwardson,et al.  Rat pancreatic acini permeabilised with streptolysin O secrete amylase at Ca2+ concentrations in the micromolar range, when provided with ATP and GTP gamma S. , 1990, Biochimica et biophysica acta.

[153]  T. Südhof,et al.  Phospholipid binding by a synaptic vesicle protein homologous to the regulatory region of protein kinase C , 1990, Nature.

[154]  D. Eberhard,et al.  Evidence that the inositol phospholipids are necessary for exocytosis. Loss of inositol phospholipids and inhibition of secretion in permeabilized cells caused by a bacterial phospholipase C and removal of ATP. , 1990, The Biochemical journal.

[155]  T. Südhof,et al.  rab3 is a small GTP-binding protein exclusively localized to synaptic vesicles. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[156]  A. Pérez,et al.  Permeable cell models in stimulus-secretion coupling. , 1990, Annual review of physiology.

[157]  J. Edwardson,et al.  A specific interaction in vitro between pancreatic zymogen granules and plasma membranes: stimulation by G-protein activators but not by Ca2+ , 1989, The Journal of cell biology.

[158]  D. Epel,et al.  Stable, resealable pores formed in sea urchin eggs by electric discharge (electroporation) permit substrate loading for assay of enzymes in vivo. , 1989, Cell regulation.

[159]  B. Gomperts,et al.  Soluble proteins as modulators of the exocytotic reaction of permeabilised rat mast cells. , 1989, Journal of cell science.

[160]  D. Aunis,et al.  A reassessment of guanine nucleotide effects on catecholamine secretion from permeabilized adrenal chromaffin cells. , 1989, The Journal of biological chemistry.

[161]  M. Geisow,et al.  A role for calpactin in calcium-dependent exocytosis in adrenal chromaffin cells , 1989, Nature.

[162]  T. Martin,et al.  A new method for cell permeabilization reveals a cytosolic protein requirement for Ca2+ -activated secretion in GH3 pituitary cells. , 1989, The Journal of biological chemistry.

[163]  D. Eberhard,et al.  MgATP-independent and MgATP-dependent exocytosis. Evidence that MgATP primes adrenal chromaffin cells to undergo exocytosis. , 1989, The Journal of biological chemistry.

[164]  S. Emr,et al.  The Saccharomyces cerevisiae SEC14 gene encodes a cytosolic factor that is required for transport of secretory proteins from the yeast Golgi complex , 1989, The Journal of cell biology.

[165]  D. Epel,et al.  The localization of PI and PIP kinase activities in the sea urchin egg and their modulation following fertilization. , 1989, Developmental biology.

[166]  R. Burgoyne,et al.  The control of cytoskeletal actin and exocytosis in intact and permeabilized adrenal chromaffin cells: role of calcium and protein kinase C. , 1989, Cellular signalling.

[167]  T. Whalley,et al.  Exocytosis reconstituted from the sea urchin egg is unaffected by calcium pretreatment of granules and plasma membrane , 1988, Bioscience reports.

[168]  P. Stahl,et al.  In vitro fusion of endosomes following receptor-mediated endocytosis. , 1988, The Journal of biological chemistry.

[169]  T. Takuma,et al.  Amylase secretion from saponin-permeabilized parotid cells evoked by cyclic AMP. , 1988, Journal of biochemistry.

[170]  D. Aunis,et al.  Loss of proteins from digitonin-permeabilized adrenal chromaffin cells essential for exocytosis. , 1987, The Journal of biological chemistry.

[171]  B. Gomperts,et al.  Essential synergy between Ca2+ and guanine nucleotides in exocytotic secretion from permeabilized rat mast cells , 1987, The Journal of cell biology.

[172]  P. Novick,et al.  A ras-like protein is required for a post-Golgi event in yeast secretion , 1987, Cell.

[173]  R. Jackson,et al.  In vitro reconstitution of exocytosis from sea urchin egg plasma membrane and isolated cortical vesicles , 1987, Bioscience reports.

[174]  C. Wollheim,et al.  Guanine nucleotides induce Ca2+-independent insulin secretion from permeabilized RINm5F cells. , 1987, The Journal of biological chemistry.

[175]  K. Howell,et al.  Reconstitution of vesicle fusions occurring in endocytosis with a cell‐free system. , 1986, The EMBO journal.

[176]  R. Holz,et al.  Catecholamine secretion from digitonin-treated PC12 cells. Effects of Ca2+, ATP, and protein kinase C activators. , 1986, The Journal of biological chemistry.

[177]  R. Neubig,et al.  Guanine nucleotide effects on catecholamine secretion from digitonin-permeabilized adrenal chromaffin cells. , 1986, The Journal of biological chemistry.

[178]  T. Martin,et al.  Characterization of Ca2+-stimulated secretion in permeable GH3 pituitary cells. , 1986, The Journal of biological chemistry.

[179]  K. Ishiguro,et al.  Calmodulin-binding protein (55K + 17K) of sea urchin eggs has a Ca2+- and calmodulin-dependent phosphoprotein phosphatase activity. , 1986, Journal of biochemistry.

[180]  M. Scrutton,et al.  Gaining access to the cytosol: the technique and some applications of electropermeabilization. , 1986, The Biochemical journal.

[181]  B. Gomperts,et al.  Two roles for guanine nucleotides in the stimulus-secretion sequence of neutrophils , 1986, Nature.

[182]  G. Warren,et al.  Reconstitution of an endocytic fusion event in a cell-free system , 1985, Cell.

[183]  R. Jackson,et al.  In vitro reconstitution of exocytosis from plasma membrane and isolated secretory vesicles , 1985, The Journal of cell biology.

[184]  J. Zimmerberg,et al.  Exocytosis of sea urchin egg cortical vesicles in vitro is retarded by hyperosmotic sucrose: kinetics of fusion monitored by quantitative light-scattering microscopy , 1985, The Journal of cell biology.

[185]  P. F. Baker,et al.  Guanine nucleotides and Ca‐dependent exocytosis , 1985, FEBS letters.

[186]  B. Shapiro,et al.  2 – The Formation of the Fertilization Membrane of the Sea Urchin Egg , 1985 .

[187]  J. Rothman,et al.  Sequential intermediates in the pathway of intercompartmental transport in a cell-free system , 1984, Cell.

[188]  D. Hoekstra,et al.  Fluorescence method for measuring the kinetics of fusion between biological membranes. , 1984, Biochemistry.

[189]  H. Sasaki,et al.  Modulation of calcium sensitivity by a specific cortical protein during sea urchin egg cortical vesicle exocytosis. , 1984, Developmental biology.

[190]  E. Neher,et al.  Capacitance measurements reveal stepwise fusion events in degranulating mast cells , 1984, Nature.

[191]  V. Vacquier,et al.  Calcium-mediated release of glucanase activity from cortical granules of sea urchin eggs. , 1983, Developmental biology.

[192]  B. Gomperts Involvement of guanine nucleotide-binding protein in the gating of Ca2+ by receptors , 1983, Nature.

[193]  D. Epel,et al.  Cortical vesicle exocytosis in isolated cortices of sea urchin eggs: description of a turbidometric assay and its utilization in studying effects of different media on discharge. , 1983, Developmental biology.

[194]  P. F. Baker,et al.  Calcium-dependent exocytosis in an in vitro secretory granule plasma membrane preparation from sea urchin eggs and the effects of some inhibitors of cytoskeletal function , 1983, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[195]  R. Holz,et al.  Catecholamine secretion from digitonin-treated adrenal medullary chromaffin cells. , 1983, The Journal of biological chemistry.

[196]  R. Jackson,et al.  Release of granule contents from sea urchin egg cortices. New assay procedures and inhibition by sulfhydryl-modifying reagents. , 1983, The Journal of biological chemistry.

[197]  J. C. Brooks,et al.  Effect of trifluoperazine on catecholamine secretion by isolated bovine adrenal medullary chromaffin cells. , 1983, Biochemical pharmacology.

[198]  R. Steinhardt,et al.  Ionic regulation of egg activation , 1982, Quarterly Reviews of Biophysics.

[199]  R. Steinhardt,et al.  Calmodulin confers calcium sensitivity on secretory exocytosis , 1982, Nature.

[200]  P. F. Baker,et al.  Calcium control of exocytosis and endocytosis in bovine adrenal medullary cells. , 1981, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[201]  L. Reichardt,et al.  Identification of a synaptic vesicle-specific membrane protein with a wide distribution in neuronal and neurosecretory tissue , 1981, The Journal of cell biology.

[202]  M. Scrutton,et al.  Direct evidence for a role for Ca2+ in amine storage granule secretion by human platelets. , 1980, Thrombosis research.

[203]  P. F. Baker,et al.  The relation between ionized calcium and cortical granule exocytosis in eggs of the sea urchin Echinus esculentus , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[204]  Baker Pf,et al.  Trifluoperazine inhibits exocytosis in sea-urchin eggs [proceedings]. , 1980 .

[205]  P. F. Baker,et al.  Influence of ATP and calcium on the cortical reaction in sea urchin eggs , 1978, Nature.

[206]  Baker Pf,et al.  A high-voltage technique for gaining rapid access to the interior of secretory cells [proceedings]. , 1978 .

[207]  R. E. Baker,et al.  Topography of cutaneous mechanoreceptive neurones in dorsal root ganglia of skin‐grafted frogs , 1978, The Journal of physiology.

[208]  H. Schuel Secretory functions of egg cortical granules in fertilization and development: A critical review , 1978 .

[209]  G. Decker,et al.  Isolation and characterization of plasma membrane-associated cortical granules from sea urchin eggs , 1977, The Journal of cell biology.

[210]  R. Zucker,et al.  Intracellular calcium release at fertilization in the sea urchin egg. , 1977, Developmental biology.

[211]  V. Vacquier The isolation of intact cortical granules from sea urchin eggs: calcium lons trigger granule discharge. , 1975, Developmental biology.

[212]  J. Meldolesi,et al.  COMPOSITION OF CELLULAR MEMBRANES IN THE PANCREAS OF THE GUINEA PIG , 1971, The Journal of cell biology.

[213]  J. Meldolesi,et al.  COMPOSITION OF CELLULAR MEMBRANES IN THE PANCREAS OF THE GUINEA PIG , 1971, The Journal of cell biology.

[214]  V. Agol,et al.  Circular structures in preparations of the replicative form of encephalomyocarditis virus RNA , 1970, FEBS letters.