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Disentangling bias between Gq, GRK2, and arrestin3 recruitment to the M3 muscarinic acetylcholine receptor

eLife, 2021-12, Vol.10

2021

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β-arrestin1 and 2 exhibit distinct phosphorylation-dependent conformations when coupling to the same GPCR in living cells

Nature communications, 2022-09, Vol.13 (1), p.5638-5638, Article 5638

2022

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A Dual GLP-1/GIP Receptor Agonist Does Not Antagonize Glucagon at Its Receptor but May Act as a Biased Agonist at the GLP-1 Receptor

International journal of molecular sciences, 2019-07, Vol.20 (14), p.3532

2019

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The Effect of Cell Surface Expression and Linker Sequence on the Recruitment of Arrestin to the GIP Receptor

Frontiers in pharmacology, 2020-08, Vol.11, p.1271-1271

2020

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Dual single-scission event analysis of constitutive transferrin receptor (TfR) endocytosis and ligand-triggered β2-adrenergic receptor (β2AR) or Mu-opioid receptor (MOR) endocytosis

Molecular biology of the cell, 2014-10, Vol.25 (19), p.3070-3080

2014

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Measurement of the millisecond activation switch of G protein-coupled receptors in living cells

Nature biotechnology, 2003-07, Vol.21 (7), p.807-812

2003

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Correction: Al-Zamel, N., et al. A Dual GLP-1/GIP Receptor Agonist Does Not Antagonize Glucagon at Its Receptor but May Act as a Biased Agonist at the GLP-1 Receptor. Int. J. Mol. Sci. 2019, 20 , 3532

International journal of molecular sciences, 2020-05, Vol.21 (9), p.3357

2020

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The GIP receptor displays higher basal activity than the GLP-1 receptor but does not recruit GRK2 or arrestin3 effectively

PloS one, 2014-09, Vol.9 (9), p.e106890

2014

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A reverse signaling pathway downstream of Sema4A controls cell migration via Scrib

The Journal of cell biology, 2017-01, Vol.216 (1), p.199-215

2017

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Differential effects of glucose‐dependent insulinotropic polypeptide receptor/glucagon‐like peptide‐1 receptor heteromerization on cell signaling when expressed in HEK‐293 cells

Pharmacology research & perspectives, 2022-10, Vol.10 (5), p.e01013-n/a

2022

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The N-termini of GRK2 and GRK3 simulate the stimulating effects of RKIP on β-adrenoceptors

Biochemical and biophysical research communications, 2019-12, Vol.520 (2), p.327-332

2019

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Differential Conformational Requirements for Activation of G Proteins and the Regulatory Proteins Arrestin and G Protein-coupled Receptor Kinase in the G Protein-coupled Receptor for Parathyroid Hormone (PTH)/PTH-related Protein

The Journal of biological chemistry, 2001-09, Vol.276 (36), p.33435-33443

2001

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FRET-based detection of M1 muscarinic acetylcholine receptor activation by orthosteric and allosteric agonists

PloS one, 2012, Vol.7 (1), p.e29946

2012

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Phosphorylation of GRK2 by Protein Kinase C Abolishes Its Inhibition by Calmodulin

The Journal of biological chemistry, 2001-01, Vol.276 (3), p.1911-1915

2001

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Residency time of agonists does not affect the stability of GPCR–arrestin complexes

British journal of pharmacology, 2022-08, Vol.179 (16), p.4107-4116

2022

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Improved Fluorescent Proteins for Single-Molecule Research in Molecular Tracking and Co-Localization

Journal of fluorescence, , Vol.15 (5), p.707-721

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μ-opioid receptors: correlation of agonist efficacy for signalling with ability to activate internalization

Molecular pharmacology, 2010-10, Vol.78 (4), p.756-766

2010

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β-Arrestin Binding to the β2-Adrenergic Receptor Requires Both Receptor Phosphorylation and Receptor Activation

The Journal of biological chemistry, 2005-03, Vol.280 (10), p.9528-9535

2005

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The Amino-terminal Domain of G-protein-coupled Receptor Kinase 2 Is a Regulatory Gβγ Binding Site

The Journal of biological chemistry, 2003-03, Vol.278 (10), p.8052-8057

2003

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SK2 channels regulate mitochondrial respiration and mitochondrial Ca2+ uptake

Cell death and differentiation, 2017-05, Vol.24 (5), p.761-773

2017

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Agonist-selective, Receptor-specific Interaction of Human P2Y Receptors with β-Arrestin-1 and -2

The Journal of biological chemistry, 2008-11, Vol.283 (45), p.30933-30941

2008

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Identification of key phosphorylation sites in PTH1R that determine arrestin3 binding and fine-tune receptor signaling

Biochemical journal, 2016-11, Vol.473 (22), p.4173-4192

2016

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Influence of G α q on the Dynamics of M 3 -Acetylcholine Receptor–G-Protein–Coupled Receptor Kinase 2 Interaction

Molecular pharmacology, 2015-01, Vol.87 (1), p.9-17

2015

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Endomorphin-2: a biased agonist at the μ-opioid receptor

Molecular pharmacology, 2012-08, Vol.82 (2), p.178-188

2012

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Disentangling bias between G q , GRK2, and arrestin3 recruitment to the M 3 muscarinic acetylcholine receptor

eLife, 2021-12, Vol.10

2021

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Disentangling bias between Gq, GRK2, and arrestin3 recruitment to the M3 muscarinic acetylcholine receptor

β-arrestin1 and 2 exhibit distinct phosphorylation-dependent conformations when coupling to the same GPCR in living cells

A Dual GLP-1/GIP Receptor Agonist Does Not Antagonize Glucagon at Its Receptor but May Act as a Biased Agonist at the GLP-1 Receptor

The Effect of Cell Surface Expression and Linker Sequence on the Recruitment of Arrestin to the GIP Receptor

Dual single-scission event analysis of constitutive transferrin receptor (TfR) endocytosis and ligand-triggered β2-adrenergic receptor (β2AR) or Mu-opioid receptor (MOR) endocytosis

Measurement of the millisecond activation switch of G protein-coupled receptors in living cells

Correction: Al-Zamel, N., et al. A Dual GLP-1/GIP Receptor Agonist Does Not Antagonize Glucagon at Its Receptor but May Act as a Biased Agonist at the GLP-1 Receptor. Int. J. Mol. Sci. 2019, 20 , 3532

The GIP receptor displays higher basal activity than the GLP-1 receptor but does not recruit GRK2 or arrestin3 effectively

A reverse signaling pathway downstream of Sema4A controls cell migration via Scrib

Differential effects of glucose‐dependent insulinotropic polypeptide receptor/glucagon‐like peptide‐1 receptor heteromerization on cell signaling when expressed in HEK‐293 cells

The N-termini of GRK2 and GRK3 simulate the stimulating effects of RKIP on β-adrenoceptors

Differential Conformational Requirements for Activation of G Proteins and the Regulatory Proteins Arrestin and G Protein-coupled Receptor Kinase in the G Protein-coupled Receptor for Parathyroid Hormone (PTH)/PTH-related Protein

FRET-based detection of M1 muscarinic acetylcholine receptor activation by orthosteric and allosteric agonists

Phosphorylation of GRK2 by Protein Kinase C Abolishes Its Inhibition by Calmodulin

Residency time of agonists does not affect the stability of GPCR–arrestin complexes

Improved Fluorescent Proteins for Single-Molecule Research in Molecular Tracking and Co-Localization

μ-opioid receptors: correlation of agonist efficacy for signalling with ability to activate internalization

β-Arrestin Binding to the β2-Adrenergic Receptor Requires Both Receptor Phosphorylation and Receptor Activation

The Amino-terminal Domain of G-protein-coupled Receptor Kinase 2 Is a Regulatory Gβγ Binding Site

SK2 channels regulate mitochondrial respiration and mitochondrial Ca2+ uptake

Agonist-selective, Receptor-specific Interaction of Human P2Y Receptors with β-Arrestin-1 and -2

Identification of key phosphorylation sites in PTH1R that determine arrestin3 binding and fine-tune receptor signaling

Influence of G α q on the Dynamics of M 3 -Acetylcholine Receptor–G-Protein–Coupled Receptor Kinase 2 Interaction

Endomorphin-2: a biased agonist at the μ-opioid receptor

Disentangling bias between G q , GRK2, and arrestin3 recruitment to the M 3 muscarinic acetylcholine receptor

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