review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Sandra Schmid | Q22095871 |
Thomas J. Pucadyil | Q38362349 | ||
P2093 | author name string | Sandra L Schmid | |
Thomas J Pucadyil | |||
P2860 | cites work | Coupling of coat assembly and vesicle budding to packaging of putative cargo receptors | Q22008843 |
Structural basis for cargo regulation of COPII coat assembly | Q24322472 | ||
GTP-dependent twisting of dynamin implicates constriction and tension in membrane fission | Q24322874 | ||
Dynamics of GBF1, a Brefeldin A-sensitive Arf1 exchange factor at the Golgi | Q24556576 | ||
ARFGAP1 promotes the formation of COPI vesicles, suggesting function as a component of the coat | Q24672898 | ||
Cargo and dynamin regulate clathrin-coated pit maturation. | Q27331778 | ||
Structure of the Sec23/24-Sar1 pre-budding complex of the COPII vesicle coat | Q27639671 | ||
Molecular mechanism of membrane recruitment of GGA by ARF in lysosomal protein transport | Q27640909 | ||
Structure and organization of coat proteins in the COPII cage | Q27646519 | ||
Structure and Membrane Interaction of Myristoylated ARF1 | Q27653413 | ||
Crystal structure at 2.2 A resolution of the pleckstrin homology domain from human dynamin | Q27730747 | ||
Sar1p N-terminal helix initiates membrane curvature and completes the fission of a COPII vesicle | Q27934415 | ||
Real-time detection reveals that effectors couple dynamin's GTP-dependent conformational changes to the membrane. | Q42963198 | ||
Real-time visualization of dynamin-catalyzed membrane fission and vesicle release | Q43141309 | ||
Lipid packing sensed by ArfGAP1 couples COPI coat disassembly to membrane bilayer curvature | Q44679419 | ||
Secretory cargo regulates the turnover of COPII subunits at single ER exit sites | Q46907625 | ||
Dynamin undergoes a GTP-dependent conformational change causing vesiculation | Q47945531 | ||
Golgi membrane dynamics imaged by freeze-etch electron microscopy: views of different membrane coatings involved in tubulation versus vesiculation | Q70488207 | ||
SEC12 encodes a guanine-nucleotide-exchange factor essential for transport vesicle budding from the ER. | Q27937857 | ||
Mechanisms of intracellular protein transport | Q28131681 | ||
Clathrin | Q28145011 | ||
Molecular anatomy of a trafficking organelle | Q28274481 | ||
Coat proteins and vesicle budding | Q28645867 | ||
Dynamin self-assembles into rings suggesting a mechanism for coated vesicle budding | Q29616586 | ||
COPII-coated vesicle formation reconstituted with purified coat proteins and chemically defined liposomes | Q29616856 | ||
Clathrin-coated vesicle formation and protein sorting: an integrated process | Q29619729 | ||
Tubular membrane invaginations coated by dynamin rings are induced by GTP-gamma S in nerve terminals | Q29620183 | ||
A binding site for SH3 domains targets dynamin to coated pits | Q30192712 | ||
Membrane curvature induced by Arf1-GTP is essential for vesicle formation. | Q30484329 | ||
A primer on vesicle budding | Q33603151 | ||
Three ways to make a vesicle | Q33938411 | ||
COP and clathrin-coated vesicle budding: different pathways, common approaches | Q34334300 | ||
Biological basket weaving: formation and function of clathrin-coated vesicles | Q34425195 | ||
Structure of the Sec13/31 COPII coat cage | Q34483894 | ||
An intramolecular signaling element that modulates dynamin function in vitro and in vivo | Q34658687 | ||
A molecular motor or a regulator? Dynamin's in a class of its own. | Q35063667 | ||
Biological membranes as bilayer couples. A molecular mechanism of drug-erythrocyte interactions | Q35116324 | ||
Comparative proteomics of clathrin-coated vesicles | Q36119198 | ||
Multiple GTP-binding proteins participate in clathrin-coated vesicle-mediated endocytosis | Q36232240 | ||
Regulation of Sar1 NH2 terminus by GTP binding and hydrolysis promotes membrane deformation to control COPII vesicle fission | Q36320575 | ||
ARFGAP1 plays a central role in coupling COPI cargo sorting with vesicle formation. | Q36321109 | ||
BAR, F-BAR (EFC) and ENTH/ANTH domains in the regulation of membrane-cytosol interfaces and membrane curvature | Q36580060 | ||
Mechanisms of COPII vesicle formation and protein sorting. | Q36742809 | ||
Structural design of cage and coat scaffolds that direct membrane traffic | Q36774855 | ||
The small G proteins of the Arf family and their regulators | Q36824194 | ||
Endocytosis: clathrin-mediated membrane budding | Q36882227 | ||
Isoform and splice-variant specific functions of dynamin-2 revealed by analysis of conditional knock-out cells. | Q36992898 | ||
The life cycle of a transport vesicle | Q37251871 | ||
GTPase cycle of dynamin is coupled to membrane squeeze and release, leading to spontaneous fission | Q37401393 | ||
Arf family GTP loading is activated by, and generates, positive membrane curvature | Q39965840 | ||
Cargo regulates clathrin-coated pit dynamics | Q40224212 | ||
Impairment of dynamin's GAP domain stimulates receptor-mediated endocytosis | Q40960042 | ||
Arf1-GTP-induced tubule formation suggests a function of Arf family proteins in curvature acquisition at sites of vesicle budding | Q41914282 | ||
Dynamin is membrane-active: lipid insertion is induced by phosphoinositides and phosphatidic acid | Q42055656 | ||
P433 | issue | 5945 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1217-1220 | |
P577 | publication date | 2009-09-01 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Conserved functions of membrane active GTPases in coated vesicle formation | |
P478 | volume | 325 |
Q55080738 | A Small-Angle Neutron Scattering Environment for In-Situ Observation of Chemical Processes. |
Q35011226 | A new role for the dynamin GTPase in the regulation of fusion pore expansion |
Q41001472 | A role for Sar1 and ARF1 GTPases during Golgi biogenesis in the protozoan parasite Trypanosoma brucei |
Q42531573 | ADP ribosylation factor 1 plays an essential role in the replication of a plant RNA virus. |
Q34927678 | ARFGAP1 promotes AP-2-dependent endocytosis. |
Q37725715 | Albumin and mammalian cell culture: implications for biotechnology applications |
Q35875489 | Anterograde trafficking of nascent α(2B)-adrenergic receptor: structural basis, roles of small GTPases |
Q30494008 | Arabidopsis dynamin-related proteins DRP2B and DRP1A participate together in clathrin-coated vesicle formation during endocytosis. |
Q30493236 | ArfGAP1 generates an Arf1 gradient on continuous lipid membranes displaying flat and curved regions. |
Q27934287 | Arl1p regulates spatial membrane organization at the trans-Golgi network through interaction with Arf-GEF Gea2p and flippase Drs2p. |
Q37615148 | Bending "on the rocks"--a cocktail of biophysical modules to build endocytic pathways |
Q37970880 | Bridging membrane and cytoskeleton dynamics in the secretory and endocytic pathways |
Q35146319 | COPI acts in both vesicular and tubular transport. |
Q37822575 | COPII-mediated vesicle formation at a glance |
Q34468056 | Cargo adaptors: structures illuminate mechanisms regulating vesicle biogenesis. |
Q41966581 | Cargo ubiquitination is essential for multivesicular body intralumenal vesicle formation |
Q33927508 | Chaperoning G protein-coupled receptors: from cell biology to therapeutics |
Q26744484 | Coat/Tether Interactions-Exception or Rule? |
Q35208451 | Coatomer and dimeric ADP ribosylation factor 1 promote distinct steps in membrane scission |
Q38647028 | Common membrane trafficking defects of disease-associated dynamin 2 mutations |
Q30580577 | Cooperative endocytosis of the endosomal SNARE protein syntaxin-8 and the potassium channel TASK-1. |
Q30494265 | Coordinated actions of actin and BAR proteins upstream of dynamin at endocytic clathrin-coated pits |
Q34170313 | Cystinosin, MPDU1, SWEETs and KDELR belong to a well-defined protein family with putative function of cargo receptors involved in vesicle trafficking |
Q21183982 | Decoding the massive genome of loblolly pine using haploid DNA and novel assembly strategies |
Q35694035 | Disruption of kv1.3 channel forward vesicular trafficking by hypoxia in human T lymphocytes |
Q50784338 | Distinct subcellular localization of tRNA-derived fragments in the infective metacyclic forms of Trypanosoma cruzi. |
Q34507970 | Dynamic assembly of the exomer secretory vesicle cargo adaptor subunits |
Q27663089 | Dynamic structure of membrane-anchored Arf•GTP |
Q33987301 | Endocytosis of nanomedicines. |
Q38170007 | Fission and fusion of the neuronal endoplasmic reticulum |
Q38022050 | From endocytosis to membrane fusion: emerging roles of dynamin in virus entry |
Q38018652 | G-protein coupled receptor resensitization-appreciating the balancing act of receptor function. |
Q83877741 | Getting active: protein sorting in endocytic recycling |
Q34444277 | Identification of interaction partners of the dynamin-like protein DynA from Bacillus subtilis. |
Q37559597 | In vitro activity of Paclitaxel-loaded polymeric expansile nanoparticles in breast cancer cells. |
Q38491068 | In-depth proteome analysis of the rubber particle of Hevea brasiliensis (para rubber tree). |
Q50069579 | Interferon regulatory factor 1-Rab27a regulated extracellular vesicles promote liver ischemia/reperfusion injury |
Q50045452 | Intersection of Endocytic and Exocytic Systems in Toxoplasma gondii. |
Q33769297 | Intracellular trafficking of guanylate-binding proteins is regulated by heterodimerization in a hierarchical manner |
Q35656173 | Intrinsic tethering activity of endosomal Rab proteins |
Q34734288 | Loss of Arabidopsis thaliana Dynamin-Related Protein 2B reveals separation of innate immune signaling pathways |
Q92413717 | Maintaining order: COG complex controls Golgi trafficking, processing, and sorting |
Q27679345 | Mechanistic Insights into Regulated Cargo Binding by ACAP1 Protein |
Q35007633 | Membrane budding |
Q24631676 | Membrane budding and scission by the ESCRT machinery: it's all in the neck |
Q41791456 | Membrane deformation and separation |
Q47654966 | Membrane scission driven by the PROPPIN Atg18. |
Q39799995 | Membrane traffic and fusion at post-Golgi compartments |
Q58570548 | Modeling Membrane Curvature Generation due to Membrane⁻Protein Interactions |
Q37616433 | Modeling membrane shaping by proteins: focus on EHD2 and N-BAR domains |
Q34476196 | Molecular regulation of lysophosphatidic acid receptor 1 trafficking to the cell surface |
Q39119129 | Multibudded tubules formed by COPII on artificial liposomes |
Q36030504 | Multiple repeat elements within the FAM21 tail link the WASH actin regulatory complex to the retromer |
Q33793896 | Multiscale simulation of protein mediated membrane remodeling |
Q37836150 | Nuclear pore complex-a coat specifically tailored for the nuclear envelope |
Q30494366 | OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation |
Q28513338 | Overlapping role of dynamin isoforms in synaptic vesicle endocytosis |
Q27025523 | Phosphoinositides in the mammalian endo-lysosomal network |
Q38125148 | Plasma membrane--cortical cytoskeleton interactions: a cell biology approach with biophysical considerations |
Q34412386 | Pom121 links two essential subcomplexes of the nuclear pore complex core to the membrane |
Q37359314 | Progranulin promotes peripheral nerve regeneration and reinnervation: role of notch signaling |
Q34979713 | RNAi screen of Salmonella invasion shows role of COPI in membrane targeting of cholesterol and Cdc42 |
Q37864676 | Rabs and other small GTPases in ciliary transport |
Q26861207 | Real-time imaging of plasma membrane deformations reveals pre-fusion membrane curvature changes and a role for dynamin in the regulation of fusion pore expansion |
Q37704673 | Recent insights into the building and cycling of synaptic vesicles |
Q52319999 | Regulation of Clathrin-Mediated Endocytosis. |
Q34421232 | Reticulon Short Hairpin Transmembrane Domains Are Used to Shape ER Tubules |
Q39357812 | Saving the neck from scission |
Q50975303 | Scission of COPI and COPII vesicles is independent of GTP hydrolysis. |
Q35759972 | Sec24p and Sec16p cooperate to regulate the GTP cycle of the COPII coat |
Q37669224 | Secretion of VEGF-165 has unique characteristics, including shedding from the plasma membrane |
Q38080412 | Secretory protein biogenesis and traffic in the early secretory pathway |
Q37970882 | Sorting nexins provide diversity for retromer-dependent trafficking events |
Q27681639 | Structural Insights into Membrane Interaction and Caveolar Targeting of Dynamin-like EHD2 |
Q27665682 | Structural basis of oligomerization in septin-like GTPase of immunity-associated protein 2 (GIMAP2) |
Q28830700 | Structural characterization of coatomer in its cytosolic state |
Q33999430 | Supported bilayers with excess membrane reservoir: a template for reconstituting membrane budding and fission |
Q57978820 | The 2018 biomembrane curvature and remodeling roadmap |
Q38064291 | The Bacillus subtilis endospore: assembly and functions of the multilayered coat. |
Q28478761 | The N-terminal amphipathic helix of the topological specificity factor MinE is associated with shaping membrane curvature |
Q28489060 | The deletion of bacterial dynamin and flotillin genes results in pleiotrophic effects on cell division, cell growth and in cell shape maintenance |
Q33639580 | The emergence of multiple particle tracking in intracellular trafficking of nanomedicines |
Q39787150 | The enlarged lysosomes in beige j cells result from decreased lysosome fission and not increased lysosome fusion |
Q47132441 | The evolution of dynamin to regulate clathrin-mediated endocytosis: speculations on the evolutionarily late appearance of dynamin relative to clathrin-mediated endocytosis |
Q36555183 | The highly conserved COPII coat complex sorts cargo from the endoplasmic reticulum and targets it to the golgi |
Q38307741 | The role of protein-protein interactions in the intracellular traffic of the potassium channels TASK-1 and TASK-3. |
Q37456127 | Toward a model for Arf GTPases as regulators of traffic at the Golgi |
Q41413341 | Trafficking and release of Leishmania metacyclic HASPB on macrophage invasion |
Q36382396 | Trafficking of an endogenous potassium channel in adult ventricular myocytes |
Q34058499 | Transport vesicle uncoating: it's later than you think |
Q34589636 | Two dynamin-2 genes are required for normal zebrafish development |
Q50061366 | Understanding the translocation mechanism of PLGA nanoparticles across round window membrane into the inner ear: a guideline for inner ear drug delivery based on nanomedicine |
Q27026111 | Vacuolar protein sorting mechanisms in plants |
Q24306063 | Versatile membrane deformation potential of activated pacsin |
Q41862482 | Vesicle formation within endosomes: An ESCRT marks the spot |
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