scholarly article | Q13442814 |
P819 | ADS bibcode | 2006PNAS..103.2138M |
P356 | DOI | 10.1073/PNAS.0507686103 |
P932 | PMC publication ID | 1413699 |
P698 | PubMed publication ID | 16461466 |
P5875 | ResearchGate publication ID | 7313731 |
P50 | author | Kai Johnsson | Q29841297 |
Karen L Martinez | Q56697486 | ||
P2093 | author name string | Nathalie George | |
Horst Vogel | |||
Ruud Hovius | |||
Jean-Manuel Segura | |||
Bruno H Meyer | |||
P2860 | cites work | Triton promotes domain formation in lipid raft mixtures | Q24537567 |
Lipid rafts and signal transduction | Q28131735 | ||
Subtypes of the somatostatin receptor assemble as functional homo- and heterodimers | Q28138304 | ||
Heterodimerization of mu and delta opioid receptors: A role in opiate synergy | Q28143344 | ||
Monitoring of ligand-independent dimerization and ligand-induced conformational changes of melatonin receptors in living cells by bioluminescence resonance energy transfer | Q28213709 | ||
Model systems, lipid rafts, and cell membranes | Q28261365 | ||
Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells | Q29547331 | ||
Fluorescence resonance energy transfer-based stoichiometry in living cells | Q34179589 | ||
Cholesterol depletion suppresses the translational diffusion of class II major histocompatibility complex proteins in the plasma membrane | Q34188496 | ||
An analytic solution to the Förster energy transfer problem in two dimensions | Q34254618 | ||
Monitoring the formation of dynamic G-protein-coupled receptor-protein complexes in living cells | Q34361815 | ||
Monomeric G-protein-coupled receptor as a functional unit | Q34431199 | ||
Dimerization: an emerging concept for G protein-coupled receptor ontogeny and function | Q34504071 | ||
The evolving role of lipid rafts and caveolae in G protein-coupled receptor signaling: implications for molecular pharmacology | Q35047674 | ||
Oligomerization of G protein-coupled receptors: past, present, and future | Q35546811 | ||
Roles of G-protein-coupled receptor dimerization | Q35622424 | ||
G protein-coupled receptor dimerization: function and ligand pharmacology | Q35814850 | ||
Selective chemical labeling of proteins in living cells | Q36035040 | ||
Distribution of a glycosylphosphatidylinositol-anchored protein at the apical surface of MDCK cells examined at a resolution of <100 A using imaging fluorescence resonance energy transfer | Q36256233 | ||
Transduction of receptor signal into modulation of effector activity by G proteins: the first 20 years or so .... | Q37896479 | ||
The dimeric nature of the gramicidin A transmembrane channel: conductance and fluorescence energy transfer studies of hybrid channels | Q39445296 | ||
Kinetics of the initial steps of G protein-coupled receptor-mediated cellular signaling revealed by single-molecule imaging | Q40388102 | ||
Biochemical and biophysical characterization of serotonin 5-HT2C receptor homodimers on the plasma membrane of living cells | Q40497731 | ||
Dynamic confinement of NK2 receptors in the plasma membrane. Improved FRAP analysis and biological relevance. | Q40528417 | ||
Heterodimerization of substance P and mu-opioid receptors regulates receptor trafficking and resensitization. | Q40628188 | ||
Quantitative assessment of beta 1- and beta 2-adrenergic receptor homo- and heterodimerization by bioluminescence resonance energy transfer | Q40702442 | ||
Lipid microdomains in cell surface membranes | Q41573449 | ||
Ligand modulation of lateral segregation of a G-protein-coupled receptor into lipid microdomains in sphingomyelin/phosphatidylcholine solid-supported bilayers | Q41864249 | ||
Two active molecular phenotypes of the tachykinin NK1 receptor revealed by G-protein fusions and mutagenesis. | Q43560293 | ||
Guanine nucleotides decrease the affinity of substance P binding to its receptor | Q43792973 | ||
A general method for the covalent labeling of fusion proteins with small molecules in vivo | Q44240675 | ||
Oligomerization of the alpha 1a- and alpha 1b-adrenergic receptor subtypes. Potential implications in receptor internalization | Q44530872 | ||
Reversible site-selective labeling of membrane proteins in live cells | Q44807774 | ||
Specific labeling of cell surface proteins with chemically diverse compounds | Q44986275 | ||
The NK1 receptor localizes to the plasma membrane microdomains, and its activation is dependent on lipid raft integrity. | Q45182312 | ||
Characterization and autoradiographic mapping of [3H]CP96,345, a nonpeptide selective NK1 receptor antagonist in guinea pig lung. | Q46640147 | ||
Selective solubilization of physalaemin-type substance P binding sites from rat brain membranes by glycodeoxycholate and NaCl | Q48356090 | ||
Constitutive Agonist-independent CCR5 Oligomerization and Antibody-mediated Clustering Occurring at Physiological Levels of Receptors | Q56648631 | ||
Rhodopsin dimers in native disc membranes | Q59056014 | ||
Glycophorin A helical transmembrane domains dimerize in phospholipid bilayers: a resonance energy transfer study | Q72413296 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2138-2143 | |
P577 | publication date | 2006-02-03 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | FRET imaging reveals that functional neurokinin-1 receptors are monomeric and reside in membrane microdomains of live cells | |
P478 | volume | 103 |
Q36983708 | A day in the life of a G protein-coupled receptor: the contribution to function of G protein-coupled receptor dimerization |
Q30538189 | ABCA1 dimer-monomer interconversion during HDL generation revealed by single-molecule imaging. |
Q92454710 | Ab Initio Derivation of the FRET Equations Resolves Old Puzzles and Suggests Measurement Strategies |
Q30364526 | Activation of G protein-coupled receptors: beyond two-state models and tertiary conformational changes. |
Q42935615 | Analysis of FRET signals in the presence of free donors and acceptors |
Q39907257 | Analysis of diffusion and binding in cells using the RICS approach |
Q38129012 | Are GPCRs still a source of new targets? |
Q34295521 | Assessing the relative stability of dimer interfaces in g protein-coupled receptors |
Q34290644 | BRET and Time-resolved FRET strategy to study GPCR oligomerization: from cell lines toward native tissues. |
Q24653438 | Cell-surface protein-protein interaction analysis with time-resolved FRET and snap-tag technologies: application to GPCR oligomerization |
Q40304513 | Characterization of an extended receptive ligand repertoire of the human olfactory receptor OR17-40 comprising structurally related compounds |
Q40025475 | Conformational cross-talk between alpha2A-adrenergic and mu-opioid receptors controls cell signaling |
Q40013918 | Constitutive and agonist-induced dimerizations of the P2Y1 receptor: relationship to internalization and scaffolding. |
Q43277954 | Construction of covalently coupled, concatameric dimers of 7TM receptors |
Q37922648 | Cross-talk and modulation of signaling between somatostatin and growth factor receptors |
Q56336641 | Determination of supramolecular structure and spatial distribution of protein complexes in living cells |
Q37177027 | Dimerization in the absence of higher-order oligomerization of the G protein-coupled secretin receptor |
Q35879672 | Dimerization of the class A G protein-coupled neurotensin receptor NTS1 alters G protein interaction |
Q24318766 | Dopamine D2 receptors form higher order oligomers at physiological expression levels |
Q41874339 | Efficiency of resonance energy transfer in homo-oligomeric complexes of proteins |
Q37959958 | FRET in Membrane Biophysics: An Overview. |
Q33356277 | Fluorescence correlation spectroscopy analysis of serotonin, adrenergic, muscarinic, and dopamine receptor dimerization: the oligomer number puzzle |
Q51766986 | Fluorescence ratiometric detection of ligand-induced receptor internalization using extracellular coiled-coil tag-probe labeling. |
Q30493203 | Formation and dissociation of M1 muscarinic receptor dimers seen by total internal reflection fluorescence imaging of single molecules |
Q35003608 | Full characterization of GPCR monomer-dimer dynamic equilibrium by single molecule imaging |
Q39947412 | Functional adhesiveness of the CX3CL1 chemokine requires its aggregation. Role of the transmembrane domain |
Q89725140 | Functional marriage in plasma membrane: Critical cholesterol level-optimal protein activity |
Q38118062 | Functional significance of serotonin receptor dimerization |
Q37421818 | G protein-coupled receptor hetero-dimerization: contribution to pharmacology and function |
Q37058647 | GPCR monomers and oligomers: it takes all kinds |
Q88607655 | GPCRs and Signal Transducers: Interaction Stoichiometry |
Q59042560 | GPCRs: Lipid-Dependent Membrane Receptors That Act as Drug Targets |
Q34256410 | Heterodimerization of serotonin receptors 5-HT1A and 5-HT7 differentially regulates receptor signalling and trafficking |
Q37120246 | How and why do GPCRs dimerize? |
Q37551248 | Illuminating the life of GPCRs |
Q91620483 | Imaging of intermittent lipid-receptor interactions reflects changes in live cell membranes upon agonist-receptor binding |
Q35751416 | In silico characterization of resonance energy transfer for disk-shaped membrane domains |
Q39869076 | In vivo modification of native carrier protein domains |
Q36317014 | Individual protomers of a G protein-coupled receptor dimer integrate distinct functional modules. |
Q44015807 | Inhibition of CaV2.3 channels by NK1 receptors is sensitive to membrane cholesterol but insensitive to caveolin-1. |
Q33492319 | Lipid raft-mediated regulation of G-protein coupled receptor signaling by ligands which influence receptor dimerization: a computational study |
Q34001726 | Lipid rafts: at a crossroad between cell biology and physics. |
Q34386803 | Magnificent seven: roles of G protein-coupled receptors in extracellular sensing in fungi |
Q36481872 | Mapping of the interaction site between sortilin and the p75 neurotrophin receptor reveals a regulatory role for the sortilin intracellular domain in p75 neurotrophin receptor shedding and apoptosis |
Q35841891 | Mapping of the localization of type 1 angiotensin receptor in membrane microdomains using bioluminescence resonance energy transfer-based sensors |
Q30441376 | Mapping the number of molecules and brightness in the laser scanning microscope |
Q37435513 | Mechanisms of Ras membrane organization and signalling: Ras on a rocker. |
Q37365679 | Modelling the interdependence between the stoichiometry of receptor oligomerization and ligand binding for a coexisting dimer/tetramer receptor system |
Q33288219 | Monomeric G protein-coupled receptor rhodopsin in solution activates its G protein transducin at the diffusion limit |
Q28266794 | Oligomer size of the serotonin 5-hydroxytryptamine 2C (5-HT2C) receptor revealed by fluorescence correlation spectroscopy with photon counting histogram analysis: evidence for homodimers without monomers or tetramers |
Q40224903 | Orexin-1 receptor-cannabinoid CB1 receptor heterodimerization results in both ligand-dependent and -independent coordinated alterations of receptor localization and function |
Q34494384 | Organization of higher-order oligomers of the serotonin₁(A) receptor explored utilizing homo-FRET in live cells |
Q45842287 | Original Fluorescent Ligand-Based Assays Open New Perspectives in G-Protein Coupled Receptor Drug Screening. |
Q30401692 | Overcoming barriers to membrane protein structure determination |
Q39849760 | Pirenzepine promotes the dimerization of muscarinic M1 receptors through a three-step binding process |
Q51228218 | Post-translational covalent labeling reveals heterogeneous mobility of individual G protein-coupled receptors in living cells. |
Q40065635 | Probing the function of ionotropic and G protein-coupled receptors in surface-confined membranes. |
Q35095066 | Progress in elucidating the structural and dynamic character of G Protein-Coupled Receptor oligomers for use in drug discovery |
Q38064051 | Quantitative intensity-based FRET approaches--a comparative snapshot |
Q37213783 | Regulated norepinephrine transporter interaction with the neurokinin-1 receptor establishes transporter subcellular localization |
Q34193318 | Regulation of GIP and GLP1 receptor cell surface expression by N-glycosylation and receptor heteromerization |
Q38618328 | Revealing G-protein-coupled receptor oligomerization at the single-molecule level through a nanoscopic lens: methods, dynamics and biological function. |
Q37791416 | Revitalizing membrane rafts: new tools and insights |
Q51741491 | Selective amine labeling of cell surface proteins guided by coiled-coil assembly. |
Q37192032 | Selective labeling of proteins with chemical probes in living cells |
Q36329391 | Sensitivity of cholecystokinin receptors to membrane cholesterol content |
Q30677207 | Single Molecule Imaging Deciphers the Relation between Mobility and Signaling of a Prototypical G Protein-coupled Receptor in Living Cells |
Q90316239 | Single Proteoliposome High-Content Analysis Reveals Differences in the Homo-Oligomerization of GPCRs |
Q39929624 | Specific oligomerization of the 5-HT1A receptor in the plasma membrane |
Q39996356 | Stimulation- and palmitoylation-dependent changes in oligomeric conformation of serotonin 5-HT1A receptors |
Q36719329 | T-cell antigen receptor triggering and lipid rafts: a matter of space and time scales. Talking Point on the involvement of lipid rafts in T-cell activation |
Q37593097 | Tachykinins and their receptors: contributions to physiological control and the mechanisms of disease |
Q38725905 | Taking care of bystander FRET in a crowded cell membrane environment |
Q47425376 | The Class-A GPCR Dopamine D2 Receptor Forms Transient Dimers Stabilized by Agonists: Detection by Single-Molecule Tracking |
Q33843032 | The Role of Substance P in Secondary Pathophysiology after Traumatic Brain Injury |
Q36481878 | The effects of transmembrane sequence and dimerization on cleavage of the p75 neurotrophin receptor by γ-secretase |
Q37340347 | The function of G-protein coupled receptors and membrane cholesterol: specific or general interaction? |
Q28659329 | The phosphopantetheinyl transferases: catalysis of a post-translational modification crucial for life |
Q35264433 | The significance of G protein-coupled receptor crystallography for drug discovery |
Q42801633 | The two NK-1 binding sites correspond to distinct, independent, and non-interconvertible receptor conformational states as confirmed by plasmon-waveguide resonance spectroscopy. |
Q33858582 | Third-party bioluminescence resonance energy transfer indicates constitutive association of membrane proteins: application to class a g-protein-coupled receptors and g-proteins |
Q27007472 | Tools for GPCR drug discovery |
Q38220868 | Tracking single molecules at work in living cells. |
Q58498251 | Transient GPI-anchored protein homodimers are units for raft organization and function |
Q41871595 | Unraveling receptor stoichiometry using bret |
Q40751195 | Visualization of Protein Interactions in Living Cells. |
Q37344383 | Visualization of protein interactions in living cells. |
Q24676768 | Visualizing odorant receptor trafficking in living cells down to the single-molecule level |
Search more.