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49 items found for "proteomics"
- Proteogenomic landscape and clinical characterization of GH-producing pituitary adenomas/somatotroph pituitary neuroendocrine tumors
In this study, we aimed to integrate the genetic alterations, protein expression profiles, transcriptomes Targeted capture sequencing and copy number analysis of 36 genes and nontargeted proteomics analysis Classification by consensus clustering using both RNA sequencing and proteomics revealed many similarities between the proteome and the transcriptome. GNAS samples identified by nontargeted proteomics and involved in G protein-coupled receptor (GPCR)
- Ep 128 with Dr. Ilana Kotliar
Ilana uses chemical biology-based methods to study the regulation and protein-protein interactions of GPCRs and a small family of accessory proteins called RAMPs. Ilana’s research is multi-disciplinary and involves a close collaboration with proteomics experts at
- Ep 139 with Dr Silvia Sposini
understanding the interplay between GPCR signalling and trafficking in neurons using microscopy and proteomics
- GPR56 signaling pathway network and its dynamics in the mesenchymal transition of glioblastoma
dynamics in the mesenchymal transition of glioblastoma Published date November 19, 2023 Abstract "G protein-coupled Thus, based on transcriptomic, proteomic, and phosphoproteomic differential expression data of GPR56
- Ep 133 with Dr. Richard Premont
For this, we have worked in three main areas: the regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK) – beta-arrestin system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways by GIT/PIX scaffolding complexes during cellular signaling, and characterizing the role of protein S-nitrosylation as a signaling In our work, we utilize methods including structural biology and proteomics, molecular biology and biochemical
- Ep 131 with Dr. Richard Premont
For this, we have worked in three main areas: the regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK) – beta-arrestin system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways by GIT/PIX scaffolding complexes during cellular signaling, and characterizing the role of protein S-nitrosylation as a signaling In our work, we utilize methods including structural biology and proteomics, molecular biology and biochemical
- Ep 132 with Dr. Richard Premont
For this, we have worked in three main areas: the regulation of G protein-coupled receptor signaling particularly by the G protein-coupled receptor kinase (GRK) – beta-arrestin system, the coordination of heterotrimeric G protein, small GTP-binding protein and protein kinase pathways by GIT/PIX scaffolding complexes during cellular signaling, and characterizing the role of protein S-nitrosylation as a signaling In our work, we utilize methods including structural biology and proteomics, molecular biology and biochemical
- AGPCR 24 Session IV
Mark2, Ultanir, Sila K.1 1Kinases and Brain Development Laboratory, The Francis Crick Institute, UK 2Proteomics My expertise includes biochemical approaches, proteomics and transcriptomics to name a few. My main topics were protein biochemistry, Drosophila husbandry, and genetics.
- Adhesion GPCR Workshop 2024 Full Agenda
Remarks Read More 10:00 AM Student Flash Presentations Health and Disease, Metabolism, Nervous System, Proteomics
- AGPCR 24 Session VI
Affinity proteomics showed the interaction of ADRGV1 with proteins enriched in astrocytes. His lab is well-known in the research on the cellular function of proteins and their networks related For his contribution towards defining the role of USH proteins in photoreceptor cell biology he received Conditionally knocking out Ryk, required for Vangl2 function, protected synapses and preserved cognitive Several adhesion G protein-coupled receptors (aGPCRs) have recently been shown to play critical roles
- AGPCR 24 Student Flash Presentations
HERE < Back to Full Agenda Student Flash Presentations Health and Disease, Metabolism, Nervous System, Proteomics Its Relevance For Adhesion GPCR Signaling In Vivo Lara-Sophie Brodmerkel Novel isoforms of adhesion G protein Recent studies implicate the dysregulation of adhesion G-Protein coupled receptors (GPCRs) in GBM development However, while its sister protein BAI1 has demonstrated tumor suppressor functions in the brain, it remains mRNAs were identified in human/mouse brain, those with a start codon in exon 2 encoding a full-length protein
- G protein-coupled estrogen receptor (GPER)/GPR30 forms a complex with the β1-adrenergic receptor, a membrane-associated guanylate kinase (MAGUK) scaffold protein, and protein kinase A anchoring protein (AKAP) 5 in MCF7 breast cancer cells
< GPCR News < GPCRs in Oncology and Immunology G protein-coupled estrogen receptor (GPER)/GPR30 forms a complex with the β1-adrenergic receptor, a membrane-associated guanylate kinase (MAGUK) scaffold protein , and protein kinase A anchoring protein (AKAP) 5 in MCF7 breast cancer cells Published date January 10, 2024 Abstract "G protein-coupled receptor 30 (GPR30), also named G protein-coupled estrogen receptor , and in turn protein kinase A anchoring protein (AKAP) 5.
- G Proteins and GPCRs in Cancer: Novel Precision Targeted and Immunotherapies
About Program Registration Logo Contest Committee Sponsors GPCR Retreat Program < Back to schedule G Proteins His research team has pioneered the study of G proteins and G protein coupled receptors (GPCRs) in human
- G protein-coupled receptor-mediated signaling of immunomodulation in tumor progression
< GPCR News < GPCRs in Oncology and Immunology G protein-coupled receptor-mediated signaling of immunomodulation in tumor progression Published date July 31, 2024 Abstract "G protein-coupled receptors (GPCRs) are Additionally, we focus on the roles of GPCRs in regulating immune checkpoint proteins involved in immune
- Signaling by Neutrophil G Protein-Coupled Receptors that Regulate the Release of Superoxide Anions
< GPCR News < GPCRs in Oncology and Immunology Signaling by Neutrophil G Protein-Coupled Receptors that Neutrophils, which express many receptors that are members of the large family of G protein-coupled receptors molecular patterns such as the N-formylated peptides that are formed during bacterial and mitochondrial protein
- Increased protease-activated receptor 1 autoantibodies are associated with severe COVID-19
< GPCR News < GPCRs in Oncology and Immunology Increased protease-activated receptor 1 autoantibodies
- G Protein-coupled Receptor-mediated Membrane Targeting of PLCγ2 is Essential for Neutrophil Chemotaxis
< GPCR News < GPCRs in Oncology and Immunology G Protein-coupled Receptor-mediated Membrane Targeting Neutrophil Chemotaxis Published date April 11, 2023 Abstract " The current dogma is that chemoattractants G protein-coupled Tags G protein-coupled receptor (GPCR) , calcium-promoted Ras inactivator (CAPRI) , chemotaxis , neutrophils
- The orphan G protein-coupled receptor 141 expressed in myeloid cells functions as an inflammation suppressor
< GPCR News < GPCRs in Oncology and Immunology The orphan G protein-coupled receptor 141 expressed in myeloid cells functions as an inflammation suppressor Published date April 29, 2024 Abstract "G protein-coupled Authors Atsuya Sawabe, Shogo Okazaki, Akira Nakamura, Ryo Goitsuka, Tomonori Kaifu Tags G protein–coupled
- CaaX-motif-adjacent residues influence G protein gamma (Gγ) prenylation under suboptimal conditions
< GPCR News < GPCRs in Oncology and Immunology CaaX-motif-adjacent residues influence G protein gamma Prenylation is an irreversible post-translational modification that supports membrane interactions of proteins Prenyltransferases tether isoprenoid lipids to proteins via a thioether linkage during prenylation. Our results also show a few hydrophobic and charged residues at the Ct are crucial determinants of a protein's findings indicate a plausible mechanism allowing for statins to differentially perturb heterotrimeric G protein
- G protein-coupled receptors: A target for microbial metabolites and a mechanistic link to microbiome-immune-brain interactions
< GPCR News < GPCRs in Oncology and Immunology G protein-coupled receptors: A target for microbial metabolites studies have demonstrated that small-molecules from gut microbiota act as ligands for specific human G protein-coupled By combining this with RNA-Seq expression and spatial localization of GPCRs from a public human protein Authors Gajender Aleti , Emily A Troyer , Suzi Hong Tags G protein-coupled receptors , Gut microbiota
- Prediction of survival and immunotherapy response by the combined classifier of G protein-coupled receptors and tumor microenvironment in melanoma
Oncology and Immunology Prediction of survival and immunotherapy response by the combined classifier of G protein-coupled Wei , Tianyi Zhang , Yu Zhu , Jia Feng , Feng Qin , Yanwen Yang , Chuanyuan Wei , Jianying Gu Tags G protein-coupled
- Systems modeling of oncogenic G-protein and GPCR signaling reveals unexpected differences in downstream pathway activation
< GPCR News < GPCRs in Oncology and Immunology Systems modeling of oncogenic G-protein and GPCR signaling In the present study, we first develop a mechanistic mathematical model of a G-protein coupled receptor
- Metallo-protease Peptidase M84 from Bacillusaltitudinis induces ROS-dependent apoptosis in ovarian cancer cells by targeting PAR-1
< GPCR News < GPCRs in Oncology and Immunology Metallo-protease Peptidase M84 from Bacillusaltitudinis Abstract "We have purified Peptidase M84 from Bacillus altitudinis in an effort to isolate anticancer proteases This metallo-protease had no discernible impact on normal cell survival, but it specifically induced
- Removing the GPCR-mediated brake on exocytosis enhances insulin action, promotes adipocyte browning, and protects against diet-induced obesity
Removing the GPCR-mediated brake on exocytosis enhances insulin action, promotes adipocyte browning, and protects Her research focuses on the structure and function of GTP binding proteins and the molecular mechanisms Her laboratory has been involved in studying G protein coupled signal transduction for many years and has made key discoveries in G protein structure and mechanisms of activation by GPCRs and activation Current areas of interest include Protease Activated Receptor signaling in the cardiovascular system
- Structural Basis for the Recognition of GPRC5D by Talquetamab, a Bispecific Antibody for Multiple Myeloma
G-protein-coupled receptor class C group 5 member D (GPRC5D), an orphan GPCR predominantly expressed GPRC5D forms a symmetric homodimer with the interface between transmembrane helix (TM) 4 of one protomer and TM4/5 of the other protomer.
- Regulator of G protein signaling 16 restrains apoptosis in colorectal cancer through disrupting TRAF6-TAB2-TAK1-JNK/p38 MAPK signaling
< GPCR News < GPCRs in Oncology and Immunology Regulator of G protein signaling 16 restrains apoptosis G protein signaling (RGS) protein family modulators play essential role within regulating downstream Our study focused on the expression patterns of RGS proteins in CRC, identifying Regulator of G protein We confirmed the elevated RGS16 protein level in CRC, and found that patients with RGS16-high tumors
- Functional Assessment of Cancer-Linked Mutations in Sensitive Regions of Regulators of G Protein Signaling Predicted by Three-Dimensional Missense Tolerance Ratio Analysis
Immunology Functional Assessment of Cancer-Linked Mutations in Sensitive Regions of Regulators of G Protein signaling (RGS) proteins modulate G protein-coupled receptor (GPCR) signaling by acting as negative regulators of G proteins. of these mutations on protein function is uncertain. signaling (RGS) proteins.
- Ep 54 with Dr. JoAnn Trejo
San Francisco under the guidance of Professor Shaun Coughlin where she worked on the newly discovered protease-activated program is to gain a thorough and mechanistic understanding of processes that control cell signaling by protease-activated Her laboratory is the recognized expert on protease-activated receptors, particularly PAR1, and over