Results 11 to 20 of about 802,072 (332)

G-Protein-Coupled Receptors [PDF]

open access: yesJournal of Biological Chemistry, 1998
G-protein-coupled receptors (GPCRs) constitute a huge family of membrane receptors to numerous hormones, neurotransmitters and diverse compounds. A large part of cardiovascular and neurological pharmacology is based upon the knowledge of these receptors and on the identification of molecules able to interfere with them, in an agonistic or antagonistic ...
Tae H. Ji, Mathis Grossmann, Inhae Ji
  +6 more sources

Lysophospholipid G Protein-coupled Receptors [PDF]

open access: yesJournal of Biological Chemistry, 2004
The many biological responses documented for lysophospholipids that include lysophosphatidic acid and sphingosine 1-phosphate can be mechanistically attributed to signaling through specific G protein-coupled receptors. At least nine receptors have now been identified, and the total number is likely to be larger.
Brigitte, Anliker, Jerold, Chun
openaire   +2 more sources

G Protein–Coupled Receptor Deorphanizations [PDF]

open access: yesAnnual Review of Pharmacology and Toxicology, 2013
G protein–coupled receptors (GPCRs) are major regulators of intercellular interactions. They initiate these actions by being activated by a wide variety of natural ligands. Historically, ligands were discovered first, but the advent of molecular biology reversed this trend.
Olivier, Civelli   +5 more
openaire   +2 more sources

Powdered G-Protein-Coupled Receptors [PDF]

open access: yesThe Journal of Physical Chemistry Letters, 2016
Preparation and storage of functional membrane proteins such as G-protein-coupled receptors (GPCRs) are crucial to the processes of drug delivery and discovery. Here, we describe a method of preparing powdered GPCRs using rhodopsin as the prototype. We purified rhodopsin in CHAPS detergent with low detergent to protein ratio so the bulk of the sample ...
Suchithranga M D C, Perera   +2 more
openaire   +2 more sources

Designer lipid-like peptides [PDF]

open access: yes, 2011
A crucial bottleneck in membrane protein studies, particularly G-protein coupled receptors, is the notorious difficulty of finding an optimal detergent that can solubilize them and maintain their stability and function. Here we report rapid production of
Baaske, Philipp   +11 more
core   +7 more sources

Atropine-functionalized gold nanoparticles binding to muscarinic receptors after passage across the intestinal epithelium

open access: yesRoyal Society Open Science, 2022
Gold nanoparticles have a high potential to be a treatment of diseases by their specific drug delivery properties and multivalent receptor stimulation.
Rebecca Claßen   +4 more
doaj   +1 more source

G Protein–Coupled Receptor Heteromers [PDF]

open access: yesAnnual Review of Pharmacology and Toxicology, 2016
G protein–coupled receptors (GPCRs) compose one of the largest families of membrane proteins involved in intracellular signaling. They are involved in numerous physiological and pathological processes and are prime candidates for drug development. Over the past decade, an increasing number of studies have reported heteromerization between GPCRs.
Gomes, Ivone   +5 more
openaire   +3 more sources

Constitutive Activity among Orphan Class-A G Protein Coupled Receptors. [PDF]

open access: yesPLoS ONE, 2015
The purpose of this study was to evaluate the extent of constitutive activity among orphan class-A G protein coupled receptors within the cAMP signaling pathway.
Adam L Martin   +2 more
doaj   +1 more source

Rules and mechanisms governing G protein coupling selectivity of GPCRs

open access: yesCell Reports, 2023
Summary: G protein-coupled receptors (GPCRs) convert extracellular stimuli into intracellular signaling by coupling to heterotrimeric G proteins of four classes: Gi/o, Gq, Gs, and G12/13.
Ikuo Masuho   +8 more
doaj   +1 more source

Interaction of the Xanthine Nucleotide Binding Goα Mutant with G Protein-coupled Receptors [PDF]

open access: yes, 1998
We constructed a double mutant version of the α subunit of Go that was regulated by xanthine nucleotides instead of guanine nucleotides (GoαX). We investigated the interaction between GoαX and G protein-coupled receptors in vitro.
Simon, Melvin I., Yu, Bo
core   +1 more source

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