Rapid preparation of bioluminescent tracers for relaxin family peptides using sortase-catalysed ligation
暂无分享,去创建一个
Zhan-Yun Guo | Jia-hui Wang | Zeng-guang Xu | Wei Nie | X. Shao | Meng-Jun Hu | Dian Wei | Ya‐Li Liu
[1] J. Wade,et al. Relaxin family peptides: structure–activity relationship studies , 2017, British journal of pharmacology.
[2] R. Ivell,et al. Relaxin‐like peptides in male reproduction – a human perspective , 2017, British journal of pharmacology.
[3] Zhan-Yun Guo,et al. Novel Bioluminescent Binding Assays for Ligand–Receptor Interaction Studies of the Fibroblast Growth Factor Family , 2016, PloS one.
[4] H. Ploegh,et al. Recent advances in sortase-catalyzed ligation methodology. , 2016, Current opinion in structural biology.
[5] Zhan-Yun Guo,et al. Identification of hydrophobic interactions between relaxin-3 and its receptor RXFP3: implication for a conformational change in the B-chain C-terminus during receptor binding , 2016, Amino Acids.
[6] Zhan-Yun Guo,et al. Novel bioluminescent binding assays for interaction studies of protein/peptide hormones with their receptors , 2016, Amino Acids.
[7] Zhan-Yun Guo,et al. Application of the novel bioluminescent ligand–receptor binding assay to relaxin-RXFP1 system for interaction studies , 2016, Amino Acids.
[8] Zhan-Yun Guo,et al. Quick preparation of nanoluciferase-based tracers for novel bioluminescent receptor-binding assays of protein hormones: Using erythropoietin as a model. , 2015, Journal of photochemistry and photobiology. B, Biology.
[9] N. Voloshchuk,et al. Sortase A Mediated Protein Modifications and Peptide Conjugations. , 2015, Current drug discovery technologies.
[10] K. Acharya,et al. Molecular features of the sortase enzyme family , 2015, The FEBS journal.
[11] Zhan-Yun Guo,et al. Novel bioluminescent receptor-binding assays for peptide hormones: using ghrelin as a model , 2015, Amino Acids.
[12] T. Dschietzig,et al. International Union of Basic and Clinical Pharmacology. XCV. Recent Advances in the Understanding of the Pharmacology and Biological Roles of Relaxin Family Peptide Receptors 1–4, the Receptors for Relaxin Family Peptides , 2015, Pharmacological Reviews.
[13] Zhan-Yun Guo,et al. Nanoluciferase as a novel quantitative protein fusion tag: Application for overexpression and bioluminescent receptor-binding assays of human leukemia inhibitory factor. , 2014, Biochimie.
[14] D. Schwarzer,et al. Sortase-mediated ligations for the site-specific modification of proteins. , 2014, Current opinion in chemical biology.
[15] M. Ritzefeld. Sortagging: A Robust and Efficient Chemoenzymatic Ligation Strategy , 2014 .
[16] D. Missiakas,et al. Sec-secretion and sortase-mediated anchoring of proteins in Gram-positive bacteria. , 2014, Biochimica et biophysica acta.
[17] Zhan-Yun Guo,et al. A novel ultrasensitive bioluminescent receptor-binding assay of INSL3 through chemical conjugation with nanoluciferase. , 2013, Biochimie.
[18] Zhan-Yun Guo,et al. A convenient method for europium‐labeling of a recombinant chimeric relaxin family peptide R3/I5 for receptor‐binding assays , 2013, Journal of peptide science : an official publication of the European Peptide Society.
[19] R. Clubb,et al. Sortase enzymes in Gram‐positive bacteria , 2011, Molecular microbiology.
[20] J. Wade,et al. General method for selective labelling of double‐chain cysteine‐rich peptides with a lanthanide chelate via solid‐phase synthesis , 2011, Journal of peptide science : an official publication of the European Peptide Society.
[21] M. Trevethick,et al. Ligand binding assays at equilibrium: validation and interpretation , 2010, British journal of pharmacology.
[22] Rainer Bischoff,et al. Receptor-ligand binding assays: technologies and applications. , 2005, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
[23] P. Bonaventure,et al. INSL5 Is a High Affinity Specific Agonist for GPCR142 (GPR100)* , 2005, Journal of Biological Chemistry.
[24] P. Bonaventure,et al. Relaxin-3/Insulin-Like Peptide 5 Chimeric Peptide, a Selective Ligand for G Protein-Coupled Receptor (GPCR)135 and GPCR142 over Leucine-Rich Repeat-Containing G Protein-Coupled Receptor 7 , 2005, Molecular Pharmacology.
[25] B. Roland,et al. Identification of Relaxin-3/INSL7 as an Endogenous Ligand for the Orphan G-protein-coupled Receptor GPCR135* , 2003, Journal of Biological Chemistry.
[26] B. Roland,et al. Identification of Relaxin-3/INSL7 as a Ligand for GPCR142* , 2003, Journal of Biological Chemistry.
[27] S. Sudo,et al. H3 Relaxin Is a Specific Ligand for LGR7 and Activates the Receptor by Interacting with Both the Ectodomain and the Exoloop 2* , 2003, The Journal of Biological Chemistry.
[28] J. Wade,et al. INSL3/Leydig Insulin-like Peptide Activates the LGR8 Receptor Important in Testis Descent* , 2002, The Journal of Biological Chemistry.
[29] A. Hsueh,et al. Activation of Orphan Receptors by the Hormone Relaxin , 2002, Science.
[30] Zhan-Yun Guo,et al. Bioluminescent Ligand-Receptor Binding Assays for Protein or Peptide Hormones. , 2016, Methods in molecular biology.
[31] J. Wade,et al. Synthetic relaxins. , 2014, Current opinion in chemical biology.
[32] R. Summers,et al. Relaxin family peptides and their receptors. , 2013, Physiological reviews.
[33] A. Davenport,et al. Radioligand binding assays and their analysis. , 2012, Methods in molecular biology.
[34] M. Keen. Radioligand-binding methods for membrane preparations and intact cells. , 1997, Methods in molecular biology.