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Identifying the binding mechanism of LEAP2 to receptor GHSR1a

The FEBS journal, 2019-04, Vol.286 (7), p.1332-1345

2019

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FAM237A, rather than peptide PEN and proCCK56‐63, binds to and activates the orphan receptor GPR83

The FEBS journal, 2023-07, Vol.290 (13), p.3461-3479

2023

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Development of a general bioluminescent activity assay for peptide ligases

The FEBS journal, 2022-09, Vol.289 (17), p.5241-5258

2022

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LEAP2 has antagonized the ghrelin receptor GHSR1a since its emergence in ancient fish

Amino acids, 2021-06, Vol.53 (6), p.939-949

2021

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Novel Bioluminescent Binding Assays for Ligand-Receptor Interaction Studies of the Fibroblast Growth Factor Family

PloS one, 2016-07, Vol.11 (7), p.e0159263-e0159263

2016

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Development of a novel ligand binding assay for relaxin family peptide receptor 3 and 4 using NanoLuc complementation

Amino acids, 2018-08, Vol.50 (8), p.1111-1119

2018

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Development of a selective agonist for relaxin family peptide receptor 3

Scientific reports, 2017-06, Vol.7 (1), p.3230-9, Article 3230

2017

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Functionality of an absolutely conserved glycine residue in the chimeric relaxin family peptide R3/I5

Amino acids, 2019-04, Vol.51 (4), p.619-626

2019

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Quantitative measurement of cell membrane receptor internalization by the nanoluciferase reporter: Using the G protein-coupled receptor RXFP3 as a model

Biochimica et biophysica acta, 2015-02, Vol.1848 (2), p.688-694

2015

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The electrostatic interactions of relaxin‐3 with receptor RXFP4 and the influence of its B‐chain C‐terminal conformation

The FEBS journal, 2014-07, Vol.281 (13), p.2927-2936

2014

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Design, recombinant expression and convenient A‐chain N‐terminal europium‐labelling of a fully active human relaxin‐3 analogue

The FEBS journal, 2012-04, Vol.279 (8), p.1505-1512

2012

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Three-dimensional electroanatomical mapping guidelines for the selection of pacing site to achieve cardiac resynchronization therapy

Frontiers in cardiovascular medicine, 2022-09, Vol.9, p.843969-843969

2022

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Proteome analysis of hepatocellular carcinoma cell strains, MHCC97-H and MHCC97-L, with different metastasis potentials

Proteomics (Weinheim), 2004-04, Vol.4 (4), p.982-994

2004

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LEAP2 is a more conserved ligand than ghrelin for fish GHSRs

Biochimie, 2023-06, Vol.209, p.10-19

2023

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Identifying key residues and key interactions for the binding of LEAP2 to receptor GHSR1a

Biochemical journal, 2020-09, Vol.477 (17), p.3199-3217

2020

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Characterization of novel M‐superfamily conotoxins with new disulfide linkage

The FEBS journal, 2006-11, Vol.273 (21), p.4972-4982

2006

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Unusual orthologs shed new light on the binding mechanism of ghrelin to its receptor GHSR1a

Archives of biochemistry and biophysics, 2021-06, Vol.704, p.108872-108872, Article 108872

2021

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Novel oral edaravone attenuates diastolic dysfunction of diabetic cardiomyopathy by activating the Nrf2 signaling pathway

European journal of pharmacology, 2022-04, Vol.920, p.174846-174846, Article 174846

2022

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Redefining left bundle branch block from high-density electroanatomical mapping

International journal of cardiology, 2024-05, Vol.402, p.131830-131830, Article 131830

2024

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Recombinant expression of an insulin-like peptide 3 (INSL3) precursor and its enzymatic conversion to mature human INSL3

The FEBS journal, 2009-09, Vol.276 (18), p.5203-5211

2009

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Molecular cloning, expression and characterization of protein disulfide isomerase from Conus marmoreus

The FEBS journal, 2007-09, Vol.274 (18), p.4778-4787

2007

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Hydrophobic interactions of relaxin family peptide receptor 3 with ligands identified using a NanoBiT-based binding assay

Biochimie, 2020-10, Vol.177, p.117-126

2020

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Interaction mechanism of insulin-like peptide 5 with relaxin family peptide receptor 4

Archives of biochemistry and biophysics, 2017-04, Vol.619, p.27-34

2017

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Development of Esterase-Resistant and Highly Active Ghrelin Analogs via Thiol–Ene Click Chemistry

ACS medicinal chemistry letters, 2022-10, Vol.13 (10), p.1655-1662

2022

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Small peptides derived from the Lys active fragment of the mung bean trypsin inhibitor are fully active against trypsin

The FEBS journal, 2010, Vol.277 (1), p.224-232

2010

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Identifying the binding mechanism of LEAP2 to receptor GHSR1a

FAM237A, rather than peptide PEN and proCCK56‐63, binds to and activates the orphan receptor GPR83

Development of a general bioluminescent activity assay for peptide ligases

LEAP2 has antagonized the ghrelin receptor GHSR1a since its emergence in ancient fish

Novel Bioluminescent Binding Assays for Ligand-Receptor Interaction Studies of the Fibroblast Growth Factor Family

Development of a novel ligand binding assay for relaxin family peptide receptor 3 and 4 using NanoLuc complementation

Development of a selective agonist for relaxin family peptide receptor 3

Functionality of an absolutely conserved glycine residue in the chimeric relaxin family peptide R3/I5

Quantitative measurement of cell membrane receptor internalization by the nanoluciferase reporter: Using the G protein-coupled receptor RXFP3 as a model

The electrostatic interactions of relaxin‐3 with receptor RXFP4 and the influence of its B‐chain C‐terminal conformation

Design, recombinant expression and convenient A‐chain N‐terminal europium‐labelling of a fully active human relaxin‐3 analogue

Three-dimensional electroanatomical mapping guidelines for the selection of pacing site to achieve cardiac resynchronization therapy

Proteome analysis of hepatocellular carcinoma cell strains, MHCC97-H and MHCC97-L, with different metastasis potentials

LEAP2 is a more conserved ligand than ghrelin for fish GHSRs

Identifying key residues and key interactions for the binding of LEAP2 to receptor GHSR1a

Characterization of novel M‐superfamily conotoxins with new disulfide linkage

Unusual orthologs shed new light on the binding mechanism of ghrelin to its receptor GHSR1a

Novel oral edaravone attenuates diastolic dysfunction of diabetic cardiomyopathy by activating the Nrf2 signaling pathway

Redefining left bundle branch block from high-density electroanatomical mapping

Recombinant expression of an insulin-like peptide 3 (INSL3) precursor and its enzymatic conversion to mature human INSL3

Molecular cloning, expression and characterization of protein disulfide isomerase from Conus marmoreus

Hydrophobic interactions of relaxin family peptide receptor 3 with ligands identified using a NanoBiT-based binding assay

Interaction mechanism of insulin-like peptide 5 with relaxin family peptide receptor 4

Development of Esterase-Resistant and Highly Active Ghrelin Analogs via Thiol–Ene Click Chemistry

Small peptides derived from the Lys active fragment of the mung bean trypsin inhibitor are fully active against trypsin

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