Mapping dynamic protein interactions in MAP kinase signaling using live-cell fluorescence fluctuation spectroscopy and imaging - Wikidata - awgldk - TriplyDB

Mapping dynamic protein interactions in MAP kinase signaling using live-cell fluorescence fluctuation spectroscopy and imaging

Mapping dynamic protein interactions in MAP kinase signaling using live-cell fluorescence fluctuation spectroscopy and imaging

http://www.wikidata.org/entity/Q36299925

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SAM domain-based protein oligomerization observed by live-cell fluorescence fluctuation spectroscopy Imaging protein complex formation in the autophagy pathway: analysis of the interaction of LC3 and Atg4B(C74A) in live cells using Förster resonance energy transfer and fluorescence recovery after photobleaching GDI-mediated cell polarization in yeast provides precise spatial and temporal control of Cdc42 signaling Quantification of cytosolic interactions identifies Ede1 oligomers as key organizers of endocytosis Novel application of fluorescence lifetime and fluorescence microscopy enables quantitative access to subcellular dynamics in plant cells Screening for FtsZ Dimerization Inhibitors Using Fluorescence Cross-Correlation Spectroscopy and Surface Resonance Plasmon Analysis Enzyme Sequestration as a Tuning Point in Controlling Response Dynamics of Signalling Networks Measuring protein dynamics in live cells: protocols and practical considerations for fluorescence fluctuation microscopy Nuclear import and assembly of influenza A virus RNA polymerase studied in live cells by fluorescence cross-correlation spectroscopy.Multiple motifs regulate apical sorting of p75 via a mechanism that involves dimerization and higher-order oligomerization.Singularity in polarization: rewiring yeast cells to make two buds Flippase-mediated phospholipid asymmetry promotes fast Cdc42 recycling in dynamic maintenance of cell polarity.Protein aggregation behavior regulates cyclin transcript localization and cell-cycle control Synaptic vesicles are "primed" for fast clathrin-mediated endocytosis at the ribbon synapse.Regulation of signal duration and the statistical dynamics of kinase activation by scaffold proteins.Modular composition predicts kinase/substrate interactions.Size-based chromatography of signaling clusters in a living cell membrane Single molecule in vivo analysis of toll-like receptor 9 and CpG DNA interaction.Quantitative in vivo fluorescence cross-correlation analyses highlight the importance of competitive effects in the regulation of protein-protein interactions Dysferlin forms a dimer mediated by the C2 domains and the transmembrane domain in vitro and in living cells.Dual modes of cdc42 recycling fine-tune polarized morphogenesis.Rapid GAL gene switch of Saccharomyces cerevisiae depends on nuclear Gal3, not nucleocytoplasmic trafficking of Gal3 and Gal80 Protein scaffolds can enhance the bistability of multisite phosphorylation systems.Toward quantitative "in vivo biochemistry" with fluorescence fluctuation spectroscopy.A high-sensitivity phospho-switch triggered by Cdk1 governs chromosome morphogenesis during cell division Scaffolds: interaction platforms for cellular signalling circuits.Scaffold-mediated nucleation of protein signaling complexes: elementary principles.Nuclear physics: quantitative single-cell approaches to nuclear organization and gene expression Real-time observation of transcription initiation and elongation on an endogenous yeast gene Quantitative measurement of brightness from living cells in the presence of photodepletion Oligomeric state regulated trafficking of human platelet-activating factor acetylhydrolase type-II.Dissecting the behavior and function of MBD3 in DNA methylation homeostasis by single-molecule spectroscopy and microscopy.Eisosomes are dynamic plasma membrane domains showing pil1-lsp1 heteroligomer binding equilibrium.Inside single cells: quantitative analysis with advanced optics and nanomaterials.Analytical model for macromolecular partitioning during yeast cell division Scaffold number in yeast signaling system sets tradeoff between system output and dynamic range.Quantitative Brightness Analysis of Fluorescence Intensity Fluctuations in E. Coli.Factors affecting the quantification of biomolecular interactions by fluorescence cross-correlation spectroscopy.Inferring diffusion dynamics from FCS in heterogeneous nuclear environments.Characterization of Ternary Protein Systems In Vivo with Tricolor Heterospecies Partition Analysis.

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P2860

Mapping dynamic protein interactions in MAP kinase signaling using live-cell fluorescence fluctuation spectroscopy and imaging

http://www.wikidata.org/entity/Q36299925

description

2007 nî lūn-bûn

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Proceedings of the National Academy of Sciences of the United States of America

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Mapping dynamic protein intera ...... ation spectroscopy and imaging

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P2093

Brian D Slaughter

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Joel W Schwartz

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Rong Li

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P2860

Function of the MAPK scaffold protein, Ste5, requires a cryptic PH domain

Global analysis of protein expression in yeast

Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein

Inhibitory and activating functions for MAPK Kss1 in the S. cerevisiae filamentous-growth signalling pathway.

The Ste5 scaffold allosterically modulates signaling output of the yeast mating pathway.

A mechanism for cell-cycle regulation of MAP kinase signaling in a yeast differentiation pathway.

Ste5 tethers multiple protein kinases in the MAP kinase cascade required for mating in S. cerevisiae.

MAP kinase dynamics in response to pheromones in budding yeast.

Signaling in the yeast pheromone response pathway: specific and high-affinity interaction of the mitogen-activated protein (MAP) kinases Kss1 and Fus3 with the upstream MAP kinase kinase Ste7.

Imaging molecular interactions in living cells.

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20320-20325

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scholarly article

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10.1073/PNAS.0710336105

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51

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104

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2007-12-12T00:00:00Z

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