Journal of Biological Chemistry, ISSN 0021-9258, 2017, Volume 292, Issue 26, pp. 10998 - 11008
Myosin Vc (myoVc) is unique among vertebrate class V myosin isoforms in that it requires teams of motors to move continuously on single actin filaments. Single...
CYTOPLASMIC DYNEIN | IN-VITRO | TUG-OF-WAR | MICROTUBULES | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENSEMBLES | MOLECULAR MOTORS | LOW DUTY RATIO | INTERSECTIONS | PROCESSIVITY | Myosin Heavy Chains - chemistry | Myosin Type V - chemistry | Actin Cytoskeleton - metabolism | Myosin Type V - metabolism | Secretory Vesicles - chemistry | Secretory Vesicles - metabolism | Actin Cytoskeleton - chemistry | Myosin Heavy Chains - genetics | Myosin Heavy Chains - metabolism | Biological Transport, Active | Secretory Vesicles - genetics | Animals | Myosin Type V - genetics | Quantum Dots - chemistry | Mice | Actin Cytoskeleton - genetics | Index Medicus | myosin | single-molecule biophysics | Molecular Biophysics | imaging | protein expression | molecular motor
CYTOPLASMIC DYNEIN | IN-VITRO | TUG-OF-WAR | MICROTUBULES | BIOCHEMISTRY & MOLECULAR BIOLOGY | ENSEMBLES | MOLECULAR MOTORS | LOW DUTY RATIO | INTERSECTIONS | PROCESSIVITY | Myosin Heavy Chains - chemistry | Myosin Type V - chemistry | Actin Cytoskeleton - metabolism | Myosin Type V - metabolism | Secretory Vesicles - chemistry | Secretory Vesicles - metabolism | Actin Cytoskeleton - chemistry | Myosin Heavy Chains - genetics | Myosin Heavy Chains - metabolism | Biological Transport, Active | Secretory Vesicles - genetics | Animals | Myosin Type V - genetics | Quantum Dots - chemistry | Mice | Actin Cytoskeleton - genetics | Index Medicus | myosin | single-molecule biophysics | Molecular Biophysics | imaging | protein expression | molecular motor
Journal Article
Molecular & Cellular Proteomics, ISSN 1535-9476, 06/2007, Volume 6, Issue 6, pp. 1007 - 1017
Insulin secretory granules (ISGs) are cytoplasmic organelles of pancreatic β-cells. They are responsible for the storage and secretion of insulin. To date,...
SECRETOGRANIN-III | B-CELL | BIOGENESIS | SUBCELLULAR-DISTRIBUTION | BIOCHEMICAL RESEARCH METHODS | BINDING-PROTEIN | PANCREATIC BETA-CELLS | CHROMOGRANIN-A | IDENTIFICATION | VESICLE EXOCYTOSIS | CARBOXYPEPTIDASE-E | Reproducibility of Results | Secretory Vesicles - chemistry | Secretory Vesicles - ultrastructure | Rats | Immunoblotting | Proteins - analysis | Proteins - isolation & purification | Protein Transport | Insulin - metabolism | Animals | Proteins - metabolism | Mass Spectrometry | Proteomics | Mice | Proteins - chemistry | Insulin Secretion | Subcellular Fractions - chemistry
SECRETOGRANIN-III | B-CELL | BIOGENESIS | SUBCELLULAR-DISTRIBUTION | BIOCHEMICAL RESEARCH METHODS | BINDING-PROTEIN | PANCREATIC BETA-CELLS | CHROMOGRANIN-A | IDENTIFICATION | VESICLE EXOCYTOSIS | CARBOXYPEPTIDASE-E | Reproducibility of Results | Secretory Vesicles - chemistry | Secretory Vesicles - ultrastructure | Rats | Immunoblotting | Proteins - analysis | Proteins - isolation & purification | Protein Transport | Insulin - metabolism | Animals | Proteins - metabolism | Mass Spectrometry | Proteomics | Mice | Proteins - chemistry | Insulin Secretion | Subcellular Fractions - chemistry
Journal Article
Journal of Virology, ISSN 0022-538X, 11/2008, Volume 82, Issue 22, pp. 11228 - 11238
Article Usage Stats Services JVI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley...
TYPE-1 GAG | HIV-1 | VIROLOGY | LIPID RAFTS | MULTIVESICULAR ENDOSOMES | ROUS-SARCOMA-VIRUS | PROTEINS | CERAMIDE | IONIZATION MASS-SPECTROMETRY | QUANTITATIVE-ANALYSIS | CELL PLASMA-MEMBRANES | Cytoplasm - chemistry | Cell Line | Secretory Vesicles - chemistry | Humans | Rats | gag Gene Products, Human Immunodeficiency Virus - chemistry | Phosphatidylinositols - isolation & purification | Cell Membrane - chemistry | Animals | HIV-1 - chemistry | Mass Spectrometry | Lipids - analysis | gag Gene Products, Human Immunodeficiency Virus - genetics | Leukemia Virus, Murine - chemistry | Structure and Assembly
TYPE-1 GAG | HIV-1 | VIROLOGY | LIPID RAFTS | MULTIVESICULAR ENDOSOMES | ROUS-SARCOMA-VIRUS | PROTEINS | CERAMIDE | IONIZATION MASS-SPECTROMETRY | QUANTITATIVE-ANALYSIS | CELL PLASMA-MEMBRANES | Cytoplasm - chemistry | Cell Line | Secretory Vesicles - chemistry | Humans | Rats | gag Gene Products, Human Immunodeficiency Virus - chemistry | Phosphatidylinositols - isolation & purification | Cell Membrane - chemistry | Animals | HIV-1 - chemistry | Mass Spectrometry | Lipids - analysis | gag Gene Products, Human Immunodeficiency Virus - genetics | Leukemia Virus, Murine - chemistry | Structure and Assembly
Journal Article
Molecular Biology of the Cell, ISSN 1059-1524, 09/2011, Volume 22, Issue 18, pp. 3394 - 3409
The Vo sector of the vacuolar H+-ATPase is a multisubunit complex that forms a proteolipid pore. Among the four isoforms (a1-a4) of subunit Voa, the isoform(s)...
MEMBRANE-FUSION | NEUROTRANSMITTER TRANSPORTERS | VESICULAR TRAFFICKING | YEAST V-ATPASE | GTP-DEPENDENT EXOCYTOSIS | TRANSMEMBRANE SEGMENTS | MEDIATED CROSS-LINKING | PROTON-TRANSLOCATING ATPASE | RENAL TUBULAR-ACIDOSIS | FLUORESCENT PROTEINS | CELL BIOLOGY | Up-Regulation | Vacuolar Proton-Translocating ATPases - genetics | Alkaline Phosphatase - metabolism | Secretory Vesicles - metabolism | Neuropeptide Y - secretion | PC12 Cells | Recombinant Fusion Proteins - metabolism | Vacuolar Proton-Translocating ATPases - metabolism | Endosomes - metabolism | Protein Subunits - metabolism | Gene Knockdown Techniques | Neuropeptide Y - metabolism | Protein Isoforms - metabolism | Neurons - secretion | Neurons - metabolism | Dopamine - metabolism | Protein Subunits - genetics | Membrane Fusion | Secretory Vesicles - chemistry | Neurotransmitter Agents - metabolism | Rats | Alkaline Phosphatase - secretion | Protein Transport | Synaptotagmins - metabolism | Animals | Norepinephrine - metabolism | Recombinant Fusion Proteins - secretion | Hydrogen-Ion Concentration
MEMBRANE-FUSION | NEUROTRANSMITTER TRANSPORTERS | VESICULAR TRAFFICKING | YEAST V-ATPASE | GTP-DEPENDENT EXOCYTOSIS | TRANSMEMBRANE SEGMENTS | MEDIATED CROSS-LINKING | PROTON-TRANSLOCATING ATPASE | RENAL TUBULAR-ACIDOSIS | FLUORESCENT PROTEINS | CELL BIOLOGY | Up-Regulation | Vacuolar Proton-Translocating ATPases - genetics | Alkaline Phosphatase - metabolism | Secretory Vesicles - metabolism | Neuropeptide Y - secretion | PC12 Cells | Recombinant Fusion Proteins - metabolism | Vacuolar Proton-Translocating ATPases - metabolism | Endosomes - metabolism | Protein Subunits - metabolism | Gene Knockdown Techniques | Neuropeptide Y - metabolism | Protein Isoforms - metabolism | Neurons - secretion | Neurons - metabolism | Dopamine - metabolism | Protein Subunits - genetics | Membrane Fusion | Secretory Vesicles - chemistry | Neurotransmitter Agents - metabolism | Rats | Alkaline Phosphatase - secretion | Protein Transport | Synaptotagmins - metabolism | Animals | Norepinephrine - metabolism | Recombinant Fusion Proteins - secretion | Hydrogen-Ion Concentration
Journal Article
Vaccine, ISSN 0264-410X, 2012, Volume 30, Issue 42, pp. 6064 - 6069
Highlights â–º Outer membrane vesicles production by Neisseria meningitidis under four different conditions. â–º Glycerol in the culture medium was not consumed...
Allergy and Immunology | Bioreactor systems | Outer membrane vesicles | Neisseria meningitidis | Vaccine | Kinetics | STRAINS | MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNITY | IMMUNOLOGY | IDENTIFICATION | METABOLISM | SEQUENCE | DISEASE | FERMENTATION | OPTIMIZATION | PROTEINS | MENINGOCOCCAL VACCINE | Batch Cell Culture Techniques | Meningococcal Vaccines - biosynthesis | Lactic Acid - chemistry | Glycerol - metabolism | Secretory Vesicles - chemistry | Bioreactors | Amino Acids - chemistry | Iron-Regulatory Proteins - chemistry | Culture Media - chemistry | Neisseria meningitidis, Serogroup B - metabolism | Bacterial Outer Membrane Proteins - biosynthesis | Glycerin | Proteins | Glycerol | Lactates | stationary phase | Outer membranes | Amino acids | Membrane vesicles | Iron | Lactic acid | Vaccines
Allergy and Immunology | Bioreactor systems | Outer membrane vesicles | Neisseria meningitidis | Vaccine | Kinetics | STRAINS | MEDICINE, RESEARCH & EXPERIMENTAL | IMMUNITY | IMMUNOLOGY | IDENTIFICATION | METABOLISM | SEQUENCE | DISEASE | FERMENTATION | OPTIMIZATION | PROTEINS | MENINGOCOCCAL VACCINE | Batch Cell Culture Techniques | Meningococcal Vaccines - biosynthesis | Lactic Acid - chemistry | Glycerol - metabolism | Secretory Vesicles - chemistry | Bioreactors | Amino Acids - chemistry | Iron-Regulatory Proteins - chemistry | Culture Media - chemistry | Neisseria meningitidis, Serogroup B - metabolism | Bacterial Outer Membrane Proteins - biosynthesis | Glycerin | Proteins | Glycerol | Lactates | stationary phase | Outer membranes | Amino acids | Membrane vesicles | Iron | Lactic acid | Vaccines
Journal Article
Microbial Pathogenesis, ISSN 0882-4010, 04/2015, Volume 81, pp. 46 - 52
Outer membrane vesicles (OMVs) are well-characterized virulence factors produced by Gram-negative bacteria. Here, we isolated two clinical strains, the...
Outer membrane vesicles | Innate immunity | Acinetobacter baumannii | Virulence | Proteomics | INFECTIONS | RISK-FACTORS | MICROBIOLOGY | HAEMOPHILUS-INFLUENZAE | IMMUNOLOGY | EPITHELIAL-CELLS | BETA-LACTAMASE | PSEUDOMONAS-AERUGINOSA | LIPOPOLYSACCHARIDE | RESISTANCE | EPIDEMIOLOGY | BIOFILM FORMATION | Macrophages - physiology | Cell Line | Epithelial Cells - metabolism | Secretory Vesicles - chemistry | Electrophoresis, Polyacrylamide Gel | Humans | Secretory Vesicles - metabolism | Proteome - analysis | Bacterial Proteins - analysis | Epithelial Cells - physiology | Tandem Mass Spectrometry | Macrophages - metabolism | Animals | Cell Death | Chromatography, Liquid | Acinetobacter baumannii - isolation & purification | Virulence Factors - analysis | Mice | Acinetobacter baumannii - metabolism | Acinetobacter Infections - microbiology | Lectins | Medical colleges | Virulence (Microbiology) | Index Medicus
Outer membrane vesicles | Innate immunity | Acinetobacter baumannii | Virulence | Proteomics | INFECTIONS | RISK-FACTORS | MICROBIOLOGY | HAEMOPHILUS-INFLUENZAE | IMMUNOLOGY | EPITHELIAL-CELLS | BETA-LACTAMASE | PSEUDOMONAS-AERUGINOSA | LIPOPOLYSACCHARIDE | RESISTANCE | EPIDEMIOLOGY | BIOFILM FORMATION | Macrophages - physiology | Cell Line | Epithelial Cells - metabolism | Secretory Vesicles - chemistry | Electrophoresis, Polyacrylamide Gel | Humans | Secretory Vesicles - metabolism | Proteome - analysis | Bacterial Proteins - analysis | Epithelial Cells - physiology | Tandem Mass Spectrometry | Macrophages - metabolism | Animals | Cell Death | Chromatography, Liquid | Acinetobacter baumannii - isolation & purification | Virulence Factors - analysis | Mice | Acinetobacter baumannii - metabolism | Acinetobacter Infections - microbiology | Lectins | Medical colleges | Virulence (Microbiology) | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2015, Volume 290, Issue 1, pp. 612 - 624
Background: The mechanism by which Rab GTPases and their effectors act in tethering is not well understood. Results: An in vitro assay was developed to study...
Trafficking | BIOCHEMISTRY & MOLECULAR BIOLOGY | GDP DISSOCIATION INHIBITOR | BINDING-PROTEIN | Exocytosis | PLASMA-MEMBRANE | Membrane Reconstitution | SECRETORY PATHWAY | SEC15 PROTEIN | FAMILY | SNARE | Rab | Vesicles | POST-GOLGI VESICLES | COMPONENT | Adaptor Proteins, Signal Transducing - chemistry | Saccharomyces cerevisiae - genetics | Vesicular Transport Proteins - metabolism | rab GTP-Binding Proteins - genetics | Saccharomyces cerevisiae - metabolism | Biological Transport | Qc-SNARE Proteins - metabolism | Biological Assay | Gene Expression Regulation, Fungal | rab GTP-Binding Proteins - metabolism | Vesicular Transport Proteins - genetics | Models, Molecular | Vesicular Transport Proteins - chemistry | Saccharomyces cerevisiae Proteins - genetics | Saccharomyces cerevisiae - chemistry | Qc-SNARE Proteins - chemistry | Transport Vesicles - metabolism | Adaptor Proteins, Signal Transducing - genetics | Saccharomyces cerevisiae Proteins - metabolism | Qc-SNARE Proteins - genetics | Golgi Apparatus - metabolism | Protein Conformation | Transport Vesicles - chemistry | rab GTP-Binding Proteins - chemistry | Mutation | Adaptor Proteins, Signal Transducing - metabolism | Saccharomyces cerevisiae Proteins - chemistry | Cell Biology
Trafficking | BIOCHEMISTRY & MOLECULAR BIOLOGY | GDP DISSOCIATION INHIBITOR | BINDING-PROTEIN | Exocytosis | PLASMA-MEMBRANE | Membrane Reconstitution | SECRETORY PATHWAY | SEC15 PROTEIN | FAMILY | SNARE | Rab | Vesicles | POST-GOLGI VESICLES | COMPONENT | Adaptor Proteins, Signal Transducing - chemistry | Saccharomyces cerevisiae - genetics | Vesicular Transport Proteins - metabolism | rab GTP-Binding Proteins - genetics | Saccharomyces cerevisiae - metabolism | Biological Transport | Qc-SNARE Proteins - metabolism | Biological Assay | Gene Expression Regulation, Fungal | rab GTP-Binding Proteins - metabolism | Vesicular Transport Proteins - genetics | Models, Molecular | Vesicular Transport Proteins - chemistry | Saccharomyces cerevisiae Proteins - genetics | Saccharomyces cerevisiae - chemistry | Qc-SNARE Proteins - chemistry | Transport Vesicles - metabolism | Adaptor Proteins, Signal Transducing - genetics | Saccharomyces cerevisiae Proteins - metabolism | Qc-SNARE Proteins - genetics | Golgi Apparatus - metabolism | Protein Conformation | Transport Vesicles - chemistry | rab GTP-Binding Proteins - chemistry | Mutation | Adaptor Proteins, Signal Transducing - metabolism | Saccharomyces cerevisiae Proteins - chemistry | Cell Biology
Journal Article
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 05/2017, Volume 292, Issue 20, pp. 8342 - 8355
Human insulin is a pivotal protein hormone controlling metabolism, growth, and aging and whose malfunctioning underlies diabetes, some cancers, and...
HEXAMER | MOLECULAR-DYNAMICS | LIGAND INTERACTIONS | PANCREATIC-ISLETS | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-SITE | PARTICLE MESH EWALD | MECHANICAL CALCULATIONS | ZINC | ALLOSTERIC TRANSITION | Secretory Vesicles - chemistry | Humans | Protein Multimerization | Neurotransmitter Agents - metabolism | Secretory Vesicles - metabolism | Insulin-Secreting Cells - chemistry | Molecular Dynamics Simulation | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Insulin - chemistry | Models, Biological | Computer Simulation | Serotonin - metabolism | Protein Structure and Folding | pancreatic islet | serotonin | insulin | crystal structure | dopamine | vesicles
HEXAMER | MOLECULAR-DYNAMICS | LIGAND INTERACTIONS | PANCREATIC-ISLETS | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-SITE | PARTICLE MESH EWALD | MECHANICAL CALCULATIONS | ZINC | ALLOSTERIC TRANSITION | Secretory Vesicles - chemistry | Humans | Protein Multimerization | Neurotransmitter Agents - metabolism | Secretory Vesicles - metabolism | Insulin-Secreting Cells - chemistry | Molecular Dynamics Simulation | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Insulin - chemistry | Models, Biological | Computer Simulation | Serotonin - metabolism | Protein Structure and Folding | pancreatic islet | serotonin | insulin | crystal structure | dopamine | vesicles
Journal Article
69.
Full Text
Lipid Remodeling of Murine Epididymosomes and Spermatozoa During Epididymal Maturation
Biology of Reproduction, ISSN 0006-3363, 06/2006, Volume 74, Issue 6, pp. 1104 - 1113
We have isolated vesicular structures from mouse epididymal fluid, referred to as epididymosomes. Epididymosomes have a roughly spherical aspect and a bilayer...
Gamete biology | Epididymis | Sperm maturation | Male reproductive tract | epididymis | CHOLESTEROL | PROSTASOME-LIKE PARTICLES | gamete biology | ADENOSINE-TRIPHOSPHATASE | PLASMA-MEMBRANE | REPRODUCTIVE BIOLOGY | SPERM | MEMBRANE-VESICLES | THIN-LAYER-CHROMATOGRAPHY | sperm maturation | FATTY-ACID | SECRETION | male reproductive tract | PROTEINS | Organelles - chemistry | Spermatozoa - chemistry | Organelles - physiology | Phospholipids - analysis | Epididymis - growth & development | Male | Sexual Maturation - physiology | Membrane Lipids - chemistry | Organelles - ultrastructure | Extracellular Fluid | Cholesterol - analysis | Membrane Lipids - analysis | Arachidonic Acid - analysis | Fatty Acids, Unsaturated - analysis | Epididymis - ultrastructure | Sperm Maturation - physiology | Fatty Acids - chemistry | Secretory Vesicles - chemistry | Secretory Vesicles - ultrastructure | Fatty Acids - analysis | Sphingomyelins - analysis | Epididymis - physiology | Animals | Anisotropy | Secretory Vesicles - physiology | Spermatozoa - physiology | Mice | Spermatozoa - cytology | Spermatozoa - ultrastructure
Gamete biology | Epididymis | Sperm maturation | Male reproductive tract | epididymis | CHOLESTEROL | PROSTASOME-LIKE PARTICLES | gamete biology | ADENOSINE-TRIPHOSPHATASE | PLASMA-MEMBRANE | REPRODUCTIVE BIOLOGY | SPERM | MEMBRANE-VESICLES | THIN-LAYER-CHROMATOGRAPHY | sperm maturation | FATTY-ACID | SECRETION | male reproductive tract | PROTEINS | Organelles - chemistry | Spermatozoa - chemistry | Organelles - physiology | Phospholipids - analysis | Epididymis - growth & development | Male | Sexual Maturation - physiology | Membrane Lipids - chemistry | Organelles - ultrastructure | Extracellular Fluid | Cholesterol - analysis | Membrane Lipids - analysis | Arachidonic Acid - analysis | Fatty Acids, Unsaturated - analysis | Epididymis - ultrastructure | Sperm Maturation - physiology | Fatty Acids - chemistry | Secretory Vesicles - chemistry | Secretory Vesicles - ultrastructure | Fatty Acids - analysis | Sphingomyelins - analysis | Epididymis - physiology | Animals | Anisotropy | Secretory Vesicles - physiology | Spermatozoa - physiology | Mice | Spermatozoa - cytology | Spermatozoa - ultrastructure
Journal Article
Blood, ISSN 0006-4971, 2013, Volume 122, Issue 25, pp. 4107 - 4110
Platelet-von Willebrand factor (VWF) is stored within α-granules and accounts for ∼20% of total VWF in platelet-rich plasma. This platelet-VWF pool is distinct...
ADHESION | VIII-RELATED ANTIGEN | VONWILLEBRAND-FACTOR | PLASMA | VWF | DISEASE | HEMATOLOGY | ABO BLOOD-GROUP | HEMOSTASIS | Secretory Vesicles - chemistry | ADAM Proteins - chemistry | Blood Platelets - chemistry | ABO Blood-Group System - chemistry | Humans | Gene Expression Regulation | Platelet Activation - physiology | Secretory Vesicles - metabolism | Glycosylation | von Willebrand Factor - genetics | ADAMTS13 Protein | ADAM Proteins - metabolism | Blood Platelets - cytology | Blood Platelets - metabolism | Proteolysis | von Willebrand Factor - chemistry | HEK293 Cells | Blood Coagulation - physiology | ADAM Proteins - genetics | ABO Blood-Group System - biosynthesis | von Willebrand Factor - metabolism
ADHESION | VIII-RELATED ANTIGEN | VONWILLEBRAND-FACTOR | PLASMA | VWF | DISEASE | HEMATOLOGY | ABO BLOOD-GROUP | HEMOSTASIS | Secretory Vesicles - chemistry | ADAM Proteins - chemistry | Blood Platelets - chemistry | ABO Blood-Group System - chemistry | Humans | Gene Expression Regulation | Platelet Activation - physiology | Secretory Vesicles - metabolism | Glycosylation | von Willebrand Factor - genetics | ADAMTS13 Protein | ADAM Proteins - metabolism | Blood Platelets - cytology | Blood Platelets - metabolism | Proteolysis | von Willebrand Factor - chemistry | HEK293 Cells | Blood Coagulation - physiology | ADAM Proteins - genetics | ABO Blood-Group System - biosynthesis | von Willebrand Factor - metabolism
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 2009, Volume 1788, Issue 10, pp. 2150 - 2159
In an effort to devise a safer and more effective vaccine delivery system, outer membrane vesicles (OMVs) were engineered to have properties of intrinsically...
OMV | E. coli O157 | Vaccine vehicle | OmpA fusion | MsbB (LpxM) | PROTEIN-A | ESCHERICHIA-COLI O157-H7 | DENDRITIC CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | NEISSERIA-MENINGITIDIS | PROTECTIVE IMMUNITY | BIOPHYSICS | LIPID-A | IN-VIVO | SALMONELLA-TYPHIMURIUM | LIPOPOLYSACCHARIDE | MSBB GENE | Amino Acid Sequence | Immunoprecipitation | Mutagenesis, Site-Directed | Lipid A - metabolism | Secretory Vesicles - chemistry | Secretory Vesicles - metabolism | Molecular Sequence Data | Escherichia coli Proteins - metabolism | Epitopes | Acyltransferases - metabolism | Chromatography, Thin Layer | Mutation - genetics | Acyltransferases - genetics | Recombinant Fusion Proteins - metabolism | Genetic Engineering | Escherichia coli - genetics | Escherichia coli - metabolism | Escherichia coli Proteins - genetics | Recombinant Fusion Proteins - genetics | Antigens, Bacterial - metabolism | Proteolysis | Escherichia coli | Water quality | Lipids | Vaccines | Universities and colleges | Antigenic determinants | Index Medicus
OMV | E. coli O157 | Vaccine vehicle | OmpA fusion | MsbB (LpxM) | PROTEIN-A | ESCHERICHIA-COLI O157-H7 | DENDRITIC CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | NEISSERIA-MENINGITIDIS | PROTECTIVE IMMUNITY | BIOPHYSICS | LIPID-A | IN-VIVO | SALMONELLA-TYPHIMURIUM | LIPOPOLYSACCHARIDE | MSBB GENE | Amino Acid Sequence | Immunoprecipitation | Mutagenesis, Site-Directed | Lipid A - metabolism | Secretory Vesicles - chemistry | Secretory Vesicles - metabolism | Molecular Sequence Data | Escherichia coli Proteins - metabolism | Epitopes | Acyltransferases - metabolism | Chromatography, Thin Layer | Mutation - genetics | Acyltransferases - genetics | Recombinant Fusion Proteins - metabolism | Genetic Engineering | Escherichia coli - genetics | Escherichia coli - metabolism | Escherichia coli Proteins - genetics | Recombinant Fusion Proteins - genetics | Antigens, Bacterial - metabolism | Proteolysis | Escherichia coli | Water quality | Lipids | Vaccines | Universities and colleges | Antigenic determinants | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2010, Volume 285, Issue 10, pp. 7405 - 7416
We present evidence that venom from the Brazilian scorpion Tityus serrulatus and a purified fraction selectively cleave essential SNARE proteins within...
VENOM | FUSION | PANCREATIC ACINAR-CELLS | SNARE COMPLEX | BOTULINUM NEUROTOXINS | SINGLE-MOLECULE | BIOCHEMISTRY & MOLECULAR BIOLOGY | REGULATED EXOCYTOSIS | GUINEA-PIG | BINDING | SECRETORY GRANULES | Immunohistochemistry | Amino Acid Sequence | Guinea Pigs | Secretory Vesicles - chemistry | Pancreas, Exocrine - anatomy & histology | Secretory Vesicles - ultrastructure | R-SNARE Proteins - metabolism | Models, Molecular | Molecular Sequence Data | R-SNARE Proteins - ultrastructure | Scorpion Venoms - enzymology | Metalloproteases - metabolism | Scorpions - enzymology | Animals | Protein Isoforms - metabolism | Metalloproteases - ultrastructure | Protein Conformation | Pancreas, Exocrine - metabolism | SNARE Proteins - metabolism | Protein Structure and Folding | Enzymes | Secretion | Subcellular Organelles | Metalloprotease | Exocytosis | Protein | Organ Systems | Tissue | Vesicles | Proteases | SNAREs | Membrane | Proteolytic | Pancreas | Cell | Fusion
VENOM | FUSION | PANCREATIC ACINAR-CELLS | SNARE COMPLEX | BOTULINUM NEUROTOXINS | SINGLE-MOLECULE | BIOCHEMISTRY & MOLECULAR BIOLOGY | REGULATED EXOCYTOSIS | GUINEA-PIG | BINDING | SECRETORY GRANULES | Immunohistochemistry | Amino Acid Sequence | Guinea Pigs | Secretory Vesicles - chemistry | Pancreas, Exocrine - anatomy & histology | Secretory Vesicles - ultrastructure | R-SNARE Proteins - metabolism | Models, Molecular | Molecular Sequence Data | R-SNARE Proteins - ultrastructure | Scorpion Venoms - enzymology | Metalloproteases - metabolism | Scorpions - enzymology | Animals | Protein Isoforms - metabolism | Metalloproteases - ultrastructure | Protein Conformation | Pancreas, Exocrine - metabolism | SNARE Proteins - metabolism | Protein Structure and Folding | Enzymes | Secretion | Subcellular Organelles | Metalloprotease | Exocytosis | Protein | Organ Systems | Tissue | Vesicles | Proteases | SNAREs | Membrane | Proteolytic | Pancreas | Cell | Fusion
Journal Article
Bioscience, Biotechnology, and Biochemistry, ISSN 0916-8451, 09/2011, Volume 75, Issue 9, pp. 1848 - 1852
COPII vesicles mediate protein transport from ER to Golgi. Sec13 makes up lattice structure with Sec31 to form COPII vesicles. We analyzed expression of two...
Arabidopsis thaliana | Sec13 | vesicle transport | bimolecular fluorescence complementation (BiFC) | Sec31 | Bimolecular fluorescence complementation (BiFC) | Vesicle transport | GATEWAY BINARY VECTORS | FISSION YEAST | FUSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | GOLGI-APPARATUS | PLANT-CELLS | RETICULUM EXPORT SITES | SECRETORY PATHWAY | COAT PROTEINS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENDOPLASMIC-RETICULUM | CHEMISTRY, APPLIED | Amino Acid Sequence | Vesicular Transport Proteins - metabolism | Vesicular Transport Proteins - genetics | Cells, Cultured | COP-Coated Vesicles - metabolism | Endoplasmic Reticulum - metabolism | Molecular Sequence Data | Protein Transport - physiology | Phylogeny | COP-Coated Vesicles - chemistry | Arabidopsis - metabolism | Arabidopsis - genetics | Sequence Homology, Amino Acid | Plant Proteins - genetics | Sequence Alignment | Gene Expression Regulation, Plant | Protein Binding | Golgi Apparatus - metabolism | Plant Proteins - metabolism
Arabidopsis thaliana | Sec13 | vesicle transport | bimolecular fluorescence complementation (BiFC) | Sec31 | Bimolecular fluorescence complementation (BiFC) | Vesicle transport | GATEWAY BINARY VECTORS | FISSION YEAST | FUSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | GOLGI-APPARATUS | PLANT-CELLS | RETICULUM EXPORT SITES | SECRETORY PATHWAY | COAT PROTEINS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | ENDOPLASMIC-RETICULUM | CHEMISTRY, APPLIED | Amino Acid Sequence | Vesicular Transport Proteins - metabolism | Vesicular Transport Proteins - genetics | Cells, Cultured | COP-Coated Vesicles - metabolism | Endoplasmic Reticulum - metabolism | Molecular Sequence Data | Protein Transport - physiology | Phylogeny | COP-Coated Vesicles - chemistry | Arabidopsis - metabolism | Arabidopsis - genetics | Sequence Homology, Amino Acid | Plant Proteins - genetics | Sequence Alignment | Gene Expression Regulation, Plant | Protein Binding | Golgi Apparatus - metabolism | Plant Proteins - metabolism
Journal Article
Structure, ISSN 0969-2126, 01/2015, Volume 23, Issue 1, pp. 161 - 172
The type III secretion system (T3SS) is a large macromolecular assembly found at the surface of many pathogenic Gram-negative bacteria. Its role is to inject...
LIPOPROTEIN | NEEDLE COMPLEX | BIOPHYSICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | EXPORT | SALMONELLA | HOST | CELL BIOLOGY | Protein Structure, Secondary | Secretory Vesicles - chemistry | Membrane Microdomains - metabolism | Protein Multimerization | Secretory Pathway | Bacterial Proteins - chemistry | Secretory Vesicles - metabolism | Membrane Microdomains - chemistry | Models, Molecular | Salmonella typhimurium | Basal Bodies - metabolism | Basal Bodies - chemistry | Membrane Proteins - chemistry | Bacterial Proteins - metabolism | Membrane Proteins - metabolism | Proteins | Oligomers | Bacteria | Electron microscopy | Analysis | Genomics | Molecular biology
LIPOPROTEIN | NEEDLE COMPLEX | BIOPHYSICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | EXPORT | SALMONELLA | HOST | CELL BIOLOGY | Protein Structure, Secondary | Secretory Vesicles - chemistry | Membrane Microdomains - metabolism | Protein Multimerization | Secretory Pathway | Bacterial Proteins - chemistry | Secretory Vesicles - metabolism | Membrane Microdomains - chemistry | Models, Molecular | Salmonella typhimurium | Basal Bodies - metabolism | Basal Bodies - chemistry | Membrane Proteins - chemistry | Bacterial Proteins - metabolism | Membrane Proteins - metabolism | Proteins | Oligomers | Bacteria | Electron microscopy | Analysis | Genomics | Molecular biology
Journal Article
Nature Reviews Immunology, ISSN 1474-1733, 05/2003, Volume 3, Issue 5, pp. 361 - 370
Granule exocytosis is the main pathway for the immune elimination of virus-infected cells and tumour cells by cytotoxic T lymphocytes and natural killer cells....
MYCOBACTERIUM-TUBERCULOSIS | NATURAL-KILLER-CELLS | IN-VITRO | INDUCED APOPTOSIS | DNA FRAGMENTATION | TARGET-CELLS | IMMUNOLOGY | PROTEASE GRANZYME-A | CYTOCHROME-C RELEASE | CYTOLYTIC T-CELLS | IMMUNOLOGICAL SYNAPSE | T-Lymphocytes, Cytotoxic - immunology | Models, Immunological | Animals | Secretory Vesicles - chemistry | Granzymes | Mice | Serine Endopeptidases - metabolism | Exocytosis | Secretory Vesicles - enzymology | Apoptosis | Cytotoxicity, Immunologic
MYCOBACTERIUM-TUBERCULOSIS | NATURAL-KILLER-CELLS | IN-VITRO | INDUCED APOPTOSIS | DNA FRAGMENTATION | TARGET-CELLS | IMMUNOLOGY | PROTEASE GRANZYME-A | CYTOCHROME-C RELEASE | CYTOLYTIC T-CELLS | IMMUNOLOGICAL SYNAPSE | T-Lymphocytes, Cytotoxic - immunology | Models, Immunological | Animals | Secretory Vesicles - chemistry | Granzymes | Mice | Serine Endopeptidases - metabolism | Exocytosis | Secretory Vesicles - enzymology | Apoptosis | Cytotoxicity, Immunologic
Journal Article