Yale Journal of Biology and Medicine, ISSN 0044-0086, 2014, Volume 87, Issue 1, pp. 55 - 62
Journal Article
Nature Reviews Molecular Cell Biology, ISSN 1471-0072, 10/2000, Volume 1, Issue 1, pp. 31 - 39
Signal transduction is initiated by complex protein-protein interactions between ligands, receptors and kinases, to name only a few. It is now becoming clear...
MEMBRANE DOMAINS | FC-EPSILON-RI | TYROSINE PHOSPHORYLATION | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CROSS-LINKING | T-CELL ACTIVATION | PLASMA-MEMBRANE | CAVEOLAE MEMBRANE | GPI-ANCHORED PROTEINS | LIVING CELLS | CELL BIOLOGY | Animals | Caveolae - metabolism | Membrane Microdomains - metabolism | Models, Biological | Membrane Microdomains - chemistry | Receptors, Cell Surface - metabolism | Signal Transduction - physiology | Sphingolipids - metabolism | Molecular Structure | Phospholipids - metabolism | Cholesterol - metabolism | Endocytosis - physiology
MEMBRANE DOMAINS | FC-EPSILON-RI | TYROSINE PHOSPHORYLATION | NITRIC-OXIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CROSS-LINKING | T-CELL ACTIVATION | PLASMA-MEMBRANE | CAVEOLAE MEMBRANE | GPI-ANCHORED PROTEINS | LIVING CELLS | CELL BIOLOGY | Animals | Caveolae - metabolism | Membrane Microdomains - metabolism | Models, Biological | Membrane Microdomains - chemistry | Receptors, Cell Surface - metabolism | Signal Transduction - physiology | Sphingolipids - metabolism | Molecular Structure | Phospholipids - metabolism | Cholesterol - metabolism | Endocytosis - physiology
Journal Article
Annual Review of Cell and Developmental Biology, ISSN 1081-0706, 11/2010, Volume 26, Issue 1, pp. 285 - 314
Fluorescence imaging methods that push or break the diffraction limit of resolution (approximately 200 nm) have grown explosively. These super-resolution...
single molecule | live cell imaging | total internal reflection fluorescence microscopy (TIRFM) | light microscopy | fluorescence | super-resolution | POINT-SPREAD FUNCTION | PHOTOACTIVATED LOCALIZATION MICROSCOPY | REFLECTION FLUORESCENCE MICROSCOPY | DIFFRACTION RESOLUTION LIMIT | DEVELOPMENTAL BIOLOGY | OPTICAL RECONSTRUCTION MICROSCOPY | STED MICROSCOPY | LIVE CELLS | STRUCTURED-ILLUMINATION MICROSCOPY | CELL BIOLOGY | GROUND-STATE-DEPLETION | STIMULATED-EMISSION | Animals | Organelles - ultrastructure | Image Processing, Computer-Assisted | Microscopy, Fluorescence - methods | Nanotechnology - methods | Microscopy, Fluorescence - instrumentation | Cell research | Fluorescence microscopy | Methods
single molecule | live cell imaging | total internal reflection fluorescence microscopy (TIRFM) | light microscopy | fluorescence | super-resolution | POINT-SPREAD FUNCTION | PHOTOACTIVATED LOCALIZATION MICROSCOPY | REFLECTION FLUORESCENCE MICROSCOPY | DIFFRACTION RESOLUTION LIMIT | DEVELOPMENTAL BIOLOGY | OPTICAL RECONSTRUCTION MICROSCOPY | STED MICROSCOPY | LIVE CELLS | STRUCTURED-ILLUMINATION MICROSCOPY | CELL BIOLOGY | GROUND-STATE-DEPLETION | STIMULATED-EMISSION | Animals | Organelles - ultrastructure | Image Processing, Computer-Assisted | Microscopy, Fluorescence - methods | Nanotechnology - methods | Microscopy, Fluorescence - instrumentation | Cell research | Fluorescence microscopy | Methods
Journal Article
Nature, ISSN 0028-0836, 04/2010, Volume 464, Issue 7289, pp. 783 - 787
Epidermal growth factor receptor (EGFR) is a type I receptor tyrosine kinase, the deregulation of which has been implicated in a variety of human...
GROWTH-FACTOR RECEPTOR | DOMAIN | MECHANISM | MULTIDISCIPLINARY SCIENCES | TRACKING | SURFACE | MEMBRANES | DYNAMICS | TYROSINE KINASES | LIVE CELLS | BINDING | Cell Polarity | Receptor, Epidermal Growth Factor - agonists | Receptor, Epidermal Growth Factor - genetics | Cricetulus | Humans | Actins - metabolism | Enzyme Stability - drug effects | Thermodynamics | Receptor, Epidermal Growth Factor - metabolism | GRB2 Adaptor Protein - genetics | Diffusion | CHO Cells | Cricetinae | Signal Transduction | Cell Survival | Gene Expression Regulation | Epidermal Growth Factor - metabolism | Enzyme Activation - drug effects | Receptor, Epidermal Growth Factor - chemistry | Protein Transport | Animals | Cell Line, Tumor | Ligands | Epidermal Growth Factor - pharmacology | Kinetics | GRB2 Adaptor Protein - metabolism | Protein Multimerization - drug effects | Physiological aspects | Genetic aspects | Ligand binding (Biochemistry) | Research | Muscle proteins | Proteins | Quantum dots | Methods | Cell adhesion & migration | Binding | Receptors | Activation | Dimers | Kinases | Signalling | Dimerization
GROWTH-FACTOR RECEPTOR | DOMAIN | MECHANISM | MULTIDISCIPLINARY SCIENCES | TRACKING | SURFACE | MEMBRANES | DYNAMICS | TYROSINE KINASES | LIVE CELLS | BINDING | Cell Polarity | Receptor, Epidermal Growth Factor - agonists | Receptor, Epidermal Growth Factor - genetics | Cricetulus | Humans | Actins - metabolism | Enzyme Stability - drug effects | Thermodynamics | Receptor, Epidermal Growth Factor - metabolism | GRB2 Adaptor Protein - genetics | Diffusion | CHO Cells | Cricetinae | Signal Transduction | Cell Survival | Gene Expression Regulation | Epidermal Growth Factor - metabolism | Enzyme Activation - drug effects | Receptor, Epidermal Growth Factor - chemistry | Protein Transport | Animals | Cell Line, Tumor | Ligands | Epidermal Growth Factor - pharmacology | Kinetics | GRB2 Adaptor Protein - metabolism | Protein Multimerization - drug effects | Physiological aspects | Genetic aspects | Ligand binding (Biochemistry) | Research | Muscle proteins | Proteins | Quantum dots | Methods | Cell adhesion & migration | Binding | Receptors | Activation | Dimers | Kinases | Signalling | Dimerization
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 08/2012, Volume 109, Issue 35, pp. E2316 - E2323
Phosphoinositides (PIs) are lipid components of cell membranes that regulate a wide variety of cellular functions. Here we exploited the blue light-induced...
Polarity | Endocytosis | Rapamycin | Ruffles | Ion channel | HUMAN-DISEASE | PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE | MULTIDISCIPLINARY SCIENCES | LIGHT | BINDING-PROTEIN | ruffles | PLASMA-MEMBRANE | 4,5-BISPHOSPHATE | SPATIOTEMPORAL CONTROL | ion channel | 5-PHOSPHATASES | endocytosis | polarity | rapamycin | LIVING CELLS | PHOSPHATASES | Phosphorylation - physiology | Endocytosis - radiation effects | Humans | Actins - metabolism | Cercopithecus aethiops | Cryptochromes - genetics | Membrane Potentials - radiation effects | Phosphatidylinositol 3-Kinases - metabolism | KCNQ3 Potassium Channel - physiology | PC12 Cells | Recombinant Fusion Proteins - metabolism | Arabidopsis Proteins - metabolism | Phosphatidylinositol 4,5-Diphosphate - metabolism | Light | Binding Sites - physiology | Phosphatidylinositols - metabolism | Cell Membrane - metabolism | KCNQ2 Potassium Channel - physiology | Signal Transduction - radiation effects | Cell Membrane - radiation effects | Cryptochromes - metabolism | Arabidopsis Proteins - genetics | Phosphoric Monoester Hydrolases - genetics | Rats | Membrane Potentials - physiology | Endocytosis - physiology | Amino Acid Motifs - physiology | Phosphorylation - radiation effects | Animals | Recombinant Fusion Proteins - genetics | Signal Transduction - physiology | Phosphoric Monoester Hydrolases - metabolism | COS Cells | Biological Sciences | PNAS Plus
Polarity | Endocytosis | Rapamycin | Ruffles | Ion channel | HUMAN-DISEASE | PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE | MULTIDISCIPLINARY SCIENCES | LIGHT | BINDING-PROTEIN | ruffles | PLASMA-MEMBRANE | 4,5-BISPHOSPHATE | SPATIOTEMPORAL CONTROL | ion channel | 5-PHOSPHATASES | endocytosis | polarity | rapamycin | LIVING CELLS | PHOSPHATASES | Phosphorylation - physiology | Endocytosis - radiation effects | Humans | Actins - metabolism | Cercopithecus aethiops | Cryptochromes - genetics | Membrane Potentials - radiation effects | Phosphatidylinositol 3-Kinases - metabolism | KCNQ3 Potassium Channel - physiology | PC12 Cells | Recombinant Fusion Proteins - metabolism | Arabidopsis Proteins - metabolism | Phosphatidylinositol 4,5-Diphosphate - metabolism | Light | Binding Sites - physiology | Phosphatidylinositols - metabolism | Cell Membrane - metabolism | KCNQ2 Potassium Channel - physiology | Signal Transduction - radiation effects | Cell Membrane - radiation effects | Cryptochromes - metabolism | Arabidopsis Proteins - genetics | Phosphoric Monoester Hydrolases - genetics | Rats | Membrane Potentials - physiology | Endocytosis - physiology | Amino Acid Motifs - physiology | Phosphorylation - radiation effects | Animals | Recombinant Fusion Proteins - genetics | Signal Transduction - physiology | Phosphoric Monoester Hydrolases - metabolism | COS Cells | Biological Sciences | PNAS Plus
Journal Article
6.
Full Text
Video-rate nanoscopy using sCMOS camera-specific single-molecule localization algorithms
Nature Methods, ISSN 1548-7091, 07/2013, Volume 10, Issue 7, pp. 653 - 658
Newly developed scientific complementary metal-oxide semiconductor (sCMOS) cameras have the potential to dramatically accelerate data acquisition, enlarge the...
FLUOROPHORES | SUPERRESOLUTION MICROSCOPY | ACQUISITION | RESOLUTION | TRACKING | BIOCHEMICAL RESEARCH METHODS | FLUORESCENT PROTEINS | ENDOCYTOSIS | LIVE CELLS | LIVING CELLS | ACCURACY | Microscopy, Video - instrumentation | Signal Processing, Computer-Assisted - instrumentation | Algorithms | Semiconductors | Molecular Imaging - instrumentation | Nanotechnology - instrumentation | Image Enhancement - instrumentation | Equipment Design | Equipment Failure Analysis | Pattern Recognition, Automated - methods | Cameras | Usage | Noise | Analysis | Nanotechnology | Molecules | Video
FLUOROPHORES | SUPERRESOLUTION MICROSCOPY | ACQUISITION | RESOLUTION | TRACKING | BIOCHEMICAL RESEARCH METHODS | FLUORESCENT PROTEINS | ENDOCYTOSIS | LIVE CELLS | LIVING CELLS | ACCURACY | Microscopy, Video - instrumentation | Signal Processing, Computer-Assisted - instrumentation | Algorithms | Semiconductors | Molecular Imaging - instrumentation | Nanotechnology - instrumentation | Image Enhancement - instrumentation | Equipment Design | Equipment Failure Analysis | Pattern Recognition, Automated - methods | Cameras | Usage | Noise | Analysis | Nanotechnology | Molecules | Video
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 432 - 14
The Golgi is composed of a stack of cis, medial, trans cisternae that are biochemically distinct. The stable compartments model postulates that permanent...
GRASP65 | ORGANIZATION | STACKING | COMPLEX | PROTEIN | MICROTUBULES | PDZ DOMAIN | MULTIDISCIPLINARY SCIENCES | CELL-FREE SYSTEM | ENDOPLASMIC-RETICULUM | MATURATION | Mammals - metabolism | Fluorescence Recovery After Photobleaching | Membrane Fusion | Coated Vesicles - metabolism | Humans | Mitochondria - metabolism | Golgi Matrix Proteins | Mitochondria - ultrastructure | Animals | Biological Transport | Golgi Apparatus - metabolism | Membrane Proteins - metabolism | HeLa Cells | Golgi Apparatus - ultrastructure | Cargo | Traffic models | Compartments | Light microscopy | Communications traffic | Transport | Anterograde transport | Golgi apparatus
GRASP65 | ORGANIZATION | STACKING | COMPLEX | PROTEIN | MICROTUBULES | PDZ DOMAIN | MULTIDISCIPLINARY SCIENCES | CELL-FREE SYSTEM | ENDOPLASMIC-RETICULUM | MATURATION | Mammals - metabolism | Fluorescence Recovery After Photobleaching | Membrane Fusion | Coated Vesicles - metabolism | Humans | Mitochondria - metabolism | Golgi Matrix Proteins | Mitochondria - ultrastructure | Animals | Biological Transport | Golgi Apparatus - metabolism | Membrane Proteins - metabolism | HeLa Cells | Golgi Apparatus - ultrastructure | Cargo | Traffic models | Compartments | Light microscopy | Communications traffic | Transport | Anterograde transport | Golgi apparatus
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 6/2008, Volume 181, Issue 7, pp. 1047 - 1054
Membrane trafficking during cytokinesis is not well understood. We used advanced live cell imaging techniques to track exocytosis of single vesicles to...
Microscopy | Report | Imaging | Biological transport | Traffic | HeLa cells | Cell membranes | Cytokinesis | Exocytosis | Daughter cells | Endosomes | ANIMAL CYTOKINESIS | HIGHER-PLANTS | MIDBODY | LATE MITOSIS | SPINDLE | MECHANISMS | COMPLETION | MICROSCOPY | CLATHRIN | REVEALS | CELL BIOLOGY | Fluorescence Recovery After Photobleaching | Humans | Mammals | Recombinant Fusion Proteins - metabolism | Microscopy, Confocal | Animals | Biological Transport | Transport Vesicles - metabolism | Golgi Apparatus - metabolism | Cell Membrane - metabolism | HeLa Cells | Intracellular Membranes - metabolism | Microscopy, Fluorescence | Evaluation | Diagnostic imaging | Properties | Methods | Fluorescence microscopy
Microscopy | Report | Imaging | Biological transport | Traffic | HeLa cells | Cell membranes | Cytokinesis | Exocytosis | Daughter cells | Endosomes | ANIMAL CYTOKINESIS | HIGHER-PLANTS | MIDBODY | LATE MITOSIS | SPINDLE | MECHANISMS | COMPLETION | MICROSCOPY | CLATHRIN | REVEALS | CELL BIOLOGY | Fluorescence Recovery After Photobleaching | Humans | Mammals | Recombinant Fusion Proteins - metabolism | Microscopy, Confocal | Animals | Biological Transport | Transport Vesicles - metabolism | Golgi Apparatus - metabolism | Cell Membrane - metabolism | HeLa Cells | Intracellular Membranes - metabolism | Microscopy, Fluorescence | Evaluation | Diagnostic imaging | Properties | Methods | Fluorescence microscopy
Journal Article
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Super‐Resolution Imaging of the Golgi in Live Cells with a Bioorthogonal Ceramide Probe
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 38, pp. 10242 - 10246
We report a lipid‐based strategy to visualize Golgi structure and dynamics at super‐resolution in live cells. The method is based on two novel reagents: a...
fluorophores | membranes | bioorthogonal chemistry | click chemistry | STED | Membranes | Click chemistry | Bioorthogonal chemistry | Fluorophores | LOCALIZATION | MOLECULE | MICROSCOPY | CHEMISTRY, MULTIDISCIPLINARY | PATHWAY | SERINE PALMITOYLTRANSFERASE | SECRETION | PROTEINS | Golgi Apparatus - enzymology | Microscopy, Confocal | Coloring Agents - analysis | Cell Survival | Humans | Golgi Apparatus - metabolism | Ceramides - chemistry | HeLa Cells | Microscopy, Fluorescence | Coloring Agents - chemistry | Enzymes | Cells | Investigations | Dyes | Microscopy | Dynamics | Imaging | Lipids | Strategy | Confocal | Endoplasmic reticulum | Three dimensional
fluorophores | membranes | bioorthogonal chemistry | click chemistry | STED | Membranes | Click chemistry | Bioorthogonal chemistry | Fluorophores | LOCALIZATION | MOLECULE | MICROSCOPY | CHEMISTRY, MULTIDISCIPLINARY | PATHWAY | SERINE PALMITOYLTRANSFERASE | SECRETION | PROTEINS | Golgi Apparatus - enzymology | Microscopy, Confocal | Coloring Agents - analysis | Cell Survival | Humans | Golgi Apparatus - metabolism | Ceramides - chemistry | HeLa Cells | Microscopy, Fluorescence | Coloring Agents - chemistry | Enzymes | Cells | Investigations | Dyes | Microscopy | Dynamics | Imaging | Lipids | Strategy | Confocal | Endoplasmic reticulum | Three dimensional
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 3/2008, Volume 180, Issue 5, pp. 905 - 914
Ca²⁺ influx through plasma membrane lesions triggers a rapid repair process that was previously shown to require the exocytosis of lysosomal organelles (Reddy,...
T lymphocytes | Endocytosis | Dextrans | Neurons | Report | HeLa cells | Neurosecretory cells | Cell membranes | Exocytosis | Cells | Endosomes | NUCLEATED CELLS | RECOVERY | RESISTANT | LYSOSOMES | POLYMORPHONUCLEAR LEUKOCYTES | EXOCYTOSIS | ENLARGEOSOME | COMPLEMENT ATTACK | PROTEINS | FIBROBLASTS | CELL BIOLOGY | Sterols - metabolism | Epithelial Cells - metabolism | Calcium - metabolism | Calcium Signaling - physiology | Epithelial Cells - drug effects | Humans | Bacterial Toxins - toxicity | Streptolysins - toxicity | Cell Membrane Structures - metabolism | Time Factors | Immunity, Innate - physiology | Cell Membrane - metabolism | Membrane Proteins - metabolism | Cell Membrane - drug effects | Cell Line | Cell Membrane Structures - drug effects | Epithelial Cells - ultrastructure | Rats | Cell Membrane - ultrastructure | Reaction Time - physiology | Endocytosis - physiology | Cell Membrane Structures - ultrastructure | Animals | Wound Healing - physiology | HeLa Cells | Index Medicus
T lymphocytes | Endocytosis | Dextrans | Neurons | Report | HeLa cells | Neurosecretory cells | Cell membranes | Exocytosis | Cells | Endosomes | NUCLEATED CELLS | RECOVERY | RESISTANT | LYSOSOMES | POLYMORPHONUCLEAR LEUKOCYTES | EXOCYTOSIS | ENLARGEOSOME | COMPLEMENT ATTACK | PROTEINS | FIBROBLASTS | CELL BIOLOGY | Sterols - metabolism | Epithelial Cells - metabolism | Calcium - metabolism | Calcium Signaling - physiology | Epithelial Cells - drug effects | Humans | Bacterial Toxins - toxicity | Streptolysins - toxicity | Cell Membrane Structures - metabolism | Time Factors | Immunity, Innate - physiology | Cell Membrane - metabolism | Membrane Proteins - metabolism | Cell Membrane - drug effects | Cell Line | Cell Membrane Structures - drug effects | Epithelial Cells - ultrastructure | Rats | Cell Membrane - ultrastructure | Reaction Time - physiology | Endocytosis - physiology | Cell Membrane Structures - ultrastructure | Animals | Wound Healing - physiology | HeLa Cells | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 08/2002, Volume 418, Issue 6901, pp. 988 - 994
Central to the initiation of immune responses is recognition of peptide antigen by T lymphocytes. The cell biology of dendritic cells makes them ideally suited...
EVANESCENT-WAVE MICROSCOPY | IMMUNITY | ENDOCYTIC COMPARTMENTS | EXOCYTOSIS | MULTIDISCIPLINARY SCIENCES | INFLAMMATORY STIMULI | MACROPINOCYTOSIS | COMPLEXES | DOWN-REGULATION | SURFACE | DEVELOPMENTAL REGULATION | Membrane Glycoproteins - analysis | Stem Cells - immunology | Dendritic Cells - immunology | Mice, Inbred C57BL | Cells, Cultured | Microscopy, Video | Stem Cells - cytology | Stem Cells - metabolism | Endosomes - metabolism | Protein Transport | Antigens, CD - analysis | Endocytosis | Animals | Lysosomes - metabolism | Antigen Presentation | Histocompatibility Antigens Class II - metabolism | Cell Differentiation | Cell Membrane - metabolism | Dendritic Cells - cytology | Mice | Lysosome-Associated Membrane Glycoproteins | Dendritic Cells - metabolism | Plasma | Cellular biology | Peptides | Life cycles
EVANESCENT-WAVE MICROSCOPY | IMMUNITY | ENDOCYTIC COMPARTMENTS | EXOCYTOSIS | MULTIDISCIPLINARY SCIENCES | INFLAMMATORY STIMULI | MACROPINOCYTOSIS | COMPLEXES | DOWN-REGULATION | SURFACE | DEVELOPMENTAL REGULATION | Membrane Glycoproteins - analysis | Stem Cells - immunology | Dendritic Cells - immunology | Mice, Inbred C57BL | Cells, Cultured | Microscopy, Video | Stem Cells - cytology | Stem Cells - metabolism | Endosomes - metabolism | Protein Transport | Antigens, CD - analysis | Endocytosis | Animals | Lysosomes - metabolism | Antigen Presentation | Histocompatibility Antigens Class II - metabolism | Cell Differentiation | Cell Membrane - metabolism | Dendritic Cells - cytology | Mice | Lysosome-Associated Membrane Glycoproteins | Dendritic Cells - metabolism | Plasma | Cellular biology | Peptides | Life cycles
Journal Article
Nature Communications, ISSN 2041-1723, 2016, Volume 7, Issue 1, p. 10778
Stimulated emission depletion (STED) nanoscopy allows observations of subcellular dynamics at the nanoscale. Applications have, however, been severely limited...
STIMULATED-EMISSION | CYTOSKELETON | SUPERRESOLUTION MICROSCOPY | VESICLES | MULTIDISCIPLINARY SCIENCES | RESOLUTION | GOLGI | STED MICROSCOPY | FUSION PROTEINS | LIVING CELLS | REVEALS | Animals | Microscopy, Fluorescence - methods | Nanotechnology - methods | Humans | Heterocyclic Compounds, 4 or More Rings - chemistry | Cercopithecus aethiops | HeLa Cells | Rhodamines - chemistry | COS Cells | Luminescent Proteins
STIMULATED-EMISSION | CYTOSKELETON | SUPERRESOLUTION MICROSCOPY | VESICLES | MULTIDISCIPLINARY SCIENCES | RESOLUTION | GOLGI | STED MICROSCOPY | FUSION PROTEINS | LIVING CELLS | REVEALS | Animals | Microscopy, Fluorescence - methods | Nanotechnology - methods | Humans | Heterocyclic Compounds, 4 or More Rings - chemistry | Cercopithecus aethiops | HeLa Cells | Rhodamines - chemistry | COS Cells | Luminescent Proteins
Journal Article