Kinetics of G-protein-coupled receptor signals in intact cells. 2008

M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
Institute of Pharmacology and Toxicology, University of Würzburg, Würzburg, Germany. lohse@toxi.uni-wuerzburg.de

G-protein-coupled receptors (GPCRs) are the largest group of cell surface receptors. They are stimulated by a variety of stimuli and signal to different classes of effectors, including several types of ion channels and second messenger-generating enzymes. Recent technical advances, most importantly in the optical recording with energy transfer techniques--fluorescence and bioluminescence resonance energy transfer, FRET and BRET--, have permitted a detailed kinetic analysis of the individual steps of the signalling chain, ranging from ligand binding to the production of second messengers in intact cells. The transfer of information, which is initiated by ligand binding, triggers a signalling cascade that displays various rate-controlling steps at different levels. This review summarizes recent findings illustrating the speed and the complexity of this signalling system.

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D015290 Second Messenger Systems Systems in which an intracellular signal is generated in response to an intercellular primary messenger such as a hormone or neurotransmitter. They are intermediate signals in cellular processes such as metabolism, secretion, contraction, phototransduction, and cell growth. Examples of second messenger systems are the adenyl cyclase-cyclic AMP system, the phosphatidylinositol diphosphate-inositol triphosphate system, and the cyclic GMP system. Intracellular Second Messengers,Second Messengers,Intracellular Second Messenger,Messenger, Second,Messengers, Intracellular Second,Messengers, Second,Second Messenger,Second Messenger System,Second Messenger, Intracellular,Second Messengers, Intracellular,System, Second Messenger,Systems, Second Messenger
D015398 Signal Transduction The intracellular transfer of information (biological activation/inhibition) through a signal pathway. In each signal transduction system, an activation/inhibition signal from a biologically active molecule (hormone, neurotransmitter) is mediated via the coupling of a receptor/enzyme to a second messenger system or to an ion channel. Signal transduction plays an important role in activating cellular functions, cell differentiation, and cell proliferation. Examples of signal transduction systems are the GAMMA-AMINOBUTYRIC ACID-postsynaptic receptor-calcium ion channel system, the receptor-mediated T-cell activation pathway, and the receptor-mediated activation of phospholipases. Those coupled to membrane depolarization or intracellular release of calcium include the receptor-mediated activation of cytotoxic functions in granulocytes and the synaptic potentiation of protein kinase activation. Some signal transduction pathways may be part of larger signal transduction pathways; for example, protein kinase activation is part of the platelet activation signal pathway. Cell Signaling,Receptor-Mediated Signal Transduction,Signal Pathways,Receptor Mediated Signal Transduction,Signal Transduction Pathways,Signal Transduction Systems,Pathway, Signal,Pathway, Signal Transduction,Pathways, Signal,Pathways, Signal Transduction,Receptor-Mediated Signal Transductions,Signal Pathway,Signal Transduction Pathway,Signal Transduction System,Signal Transduction, Receptor-Mediated,Signal Transductions,Signal Transductions, Receptor-Mediated,System, Signal Transduction,Systems, Signal Transduction,Transduction, Signal,Transductions, Signal
D043562 Receptors, G-Protein-Coupled The largest family of cell surface receptors involved in SIGNAL TRANSDUCTION. They share a common structure and signal through HETEROTRIMERIC G-PROTEINS. G Protein Coupled Receptor,G-Protein-Coupled Receptor,G-Protein-Coupled Receptors,G Protein Coupled Receptors,Receptor, G-Protein-Coupled,Receptors, G Protein Coupled
D054768 G-Protein-Coupled Receptor Kinases A family of serine-threonine kinases that are specific for G-PROTEIN-COUPLED RECEPTORS. They are regulatory proteins that play a role in G-protein-coupled receptor densensitization. G-Protein-Coupled Receptor Kinase,G Protein Coupled Receptor Kinase,G Protein Coupled Receptor Kinases,Kinase, G-Protein-Coupled Receptor,Kinases, G-Protein-Coupled Receptor,Receptor Kinase, G-Protein-Coupled,Receptor Kinases, G-Protein-Coupled
D019204 GTP-Binding Proteins Regulatory proteins that act as molecular switches. They control a wide range of biological processes including: receptor signaling, intracellular signal transduction pathways, and protein synthesis. Their activity is regulated by factors that control their ability to bind to and hydrolyze GTP to GDP. EC 3.6.1.-. G-Proteins,GTP-Regulatory Proteins,Guanine Nucleotide Regulatory Proteins,G-Protein,GTP-Binding Protein,GTP-Regulatory Protein,Guanine Nucleotide Coupling Protein,G Protein,G Proteins,GTP Binding Protein,GTP Binding Proteins,GTP Regulatory Protein,GTP Regulatory Proteins,Protein, GTP-Binding,Protein, GTP-Regulatory,Proteins, GTP-Binding,Proteins, GTP-Regulatory
D019390 Arrestins Regulatory proteins that down-regulate phosphorylated G-protein membrane receptors, including rod and cone photoreceptors and adrenergic receptors.

Related Publications

M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
January 2004, Methods in molecular biology (Clifton, N.J.),
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
December 1998, Cellular and molecular life sciences : CMLS,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
April 2014, Current opinion in cell biology,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
December 2004, Biochemical Society transactions,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
September 2001, The Journal of biological chemistry,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
January 2013, Methods in enzymology,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
January 2002, Neuro-Signals,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
April 2001, Trends in pharmacological sciences,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
March 2005, Journal of biomolecular screening,
M J Lohse, and P Hein, and C Hoffmann, and V O Nikolaev, and J-P Vilardaga, and M Bünemann
February 2017, Nature chemical biology,
Copied contents to your clipboard!