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241 items found for "cryo-EM structure"
- Structural Basis for the Recognition of GPRC5D by Talquetamab, a Bispecific Antibody for Multiple Myeloma
< GPCR News < GPCRs in Oncology and Immunology Structural Basis for the Recognition of GPRC5D by Talquetamab Here, we elucidate the structure of GPRC5D complexed with the Fab fragment of talquetamab, using cryo-electron The structure offers insights for optimizing antibody design against GPRC5D for relapsed or refractory Junhyeon Park, Geun Young Mo, Jinwoo Shin, Yunje Cho Tags GPRC5D , Multiple myeloma , class C GPCR , cryo-EM structure , talquetamab Source Contribute to the GPCR News Coming soon Become a Contributor Classified
- Flash News / DrGPCR
👅🔬 Researchers have unveiled the cryo-EM structure of TAS2R14 , the most promiscuous bitter taste receptor
- Biased agonism at the GLP-1 receptor: from structure to animal models of disease
Committee Sponsors GPCR Retreat Program < Back to schedule Biased agonism at the GLP-1 receptor: from structure Patrick Sexton " Patrick Sexton is a NHMRC Senior Principal Research Fellow and Director, ARC Centre for Cryo-electron Recently, his team has applied cryo-EM to elucidation of the structure and dynamics of GPCRs. Prof.
- Ep 32 with Dr. Chris Tate
using cryo-EM. Subsequent work has focused on understanding the molecular basis of GPCR pharmacology through structure In 2016 mini-G proteins were developed as a tool for the structure determination of GPCRs in the fully , and also by electron cryo-microscopy of receptors coupled to mini G protein bound to βγ subunits. to arrestin and also the first structure of a Class D receptor.
- Ep 89 with Dr. Patrick Sexton
Australia Senior Principal Research Fellow, and Director of the Australian Research Council Centre for Cryo-electron More recently, his team has been at the forefront of the application of cryo-EM to elucidate of the structure
- Ep 83 with Dr. Jean-Philippe Pin
mechanism of this family of G protein-coupled receptors using innovative approaches, including biosensors, cryo-EM
- Session I | Adhesion GPCR Workshop 2024 | Dr. GPCR Ecosystem
without coming out of the GAIN domain or by being partially exposed, however the recent TA-bound 7TM structures Axel Brunger’s lab at Stanford University to study the structure and function of cell-adhesion proteins As part of his doctoral work in the Blacklow laboratory at Harvard Medical School, Drew studied structure-function Gregory Tall and our research primarily focuses on the structural and biochemical characterization of microscopy (cryo-EM).
- Session V | Adhesion GPCR Workshop 2024 | Dr. GPCR Ecosystem
CINVESTAV, Mexico City, Mexico October 23-25 Download PDF Program HERE < Back to Full Agenda Session V Structural mechanisms of AGPCR signaling and function Structural Determinants Of GAIN Domain Autoproteolysis And Cleavage Resistance Of Adhesion G Protein-Coupled Receptors Fabian Pohl Structural studies of the CELSR1 Here, we report the 3.8 Å cryo-EM reconstruction of the CELSR1 ECR which enables unambiguous assignment of the 14 domains within the structure.
- Ep 145 with Dr John Janetzko
Daniel Kahne and Suzanne Walker studying the structure and function of the essential human enzyme, O-GlcNAc Over the course of my graduate work, I gained experience with structural mass spectrometry and protein has made use of several techniques including various mass spectrometry approaches, single particle cryo-EM position after the recording stops. • John will prioritize getting feedback from people outside his lab to structure
- Atypical Structure and Function of Typical Chemokine Receptors
Program Registration Logo Contest Committee Sponsors GPCR Retreat Program < Back to schedule Atypical Structure
- Structure-based discovery of functionally selective 5-HT1A receptor agonists
About Program Registration Logo Contest Committee Sponsors GPCR Retreat Program < Back to schedule Structure-based
- Posters | Adhesion GPCR Workshop 2024 | Dr. GPCR Ecosystem
Here, we describe the cryo-EM reconstruction of an aGPCR, Latrophilin3/ADGRL3, and reveal that the conserved Current affiliation: Department of Structural Biology, Genentech, South San Francisco, CA, USA" About Kordon "I am a postdoctoral scholar in the Araç Lab at The University of Chicago, studying the structure Utilizing synthetic antibody fragments, I aim to understand better the structural basis of the aGPCRs
- Unbiased multitissue transcriptomic analysis reveals complex neuroendocrine regulatory networks mediated by spinal cord injury-induced immunodeficiency
The upregulated genes in the adrenal glands (hub genes: Ciart, per2, per3, cry1, and cry2) were enriched GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- GPR176 promotes fibroblast-to-myofibroblast transition in organ fibrosis progression
Authors Yasuo Okamoto, Keisuke Kitakaze, Yasuhiro Takenouchi, Rena Matsui, Daisuke Koga, Ryo Miyashima GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- The orphan G protein-coupled receptor 141 expressed in myeloid cells functions as an inflammation suppressor
Authors Atsuya Sawabe, Shogo Okazaki, Akira Nakamura, Ryo Goitsuka, Tomonori Kaifu Tags G protein–coupled GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- Ep 107 with Dr. Roger Sunahara
The structure was first snapshot of the agonist- and G protein-bound GPCR, providing valuable models Our mission is to understand the mechanism and structural bases for ligand binding and efficacy to help One example of our recent work surrounds a structure-based effort to develop ligands that specifically changes in G protein structure. The Sunahara lab has also been developing protein-based therapeutics using structure-guided design and
- In Silico Design of Novel RGS2-Galpha-q Interaction Inhibitors with Anticancer Activity
We sought to develop RGS2 inhibitors as potential chemotherapeutic agents utilizing structure-based drug Available structures of the RGS2-Gα complex were used to extract a pharmacophore model for searching Docking of identified hits to RGS2 as well as other RGS structures was used to screen the hits for potent This is the first group of RGS2 inhibitors identified by structure-based approaches and that show anticancer GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- The binding mechanism of an anti-multiple myeloma antibody to the human GPRC5D homodimer
Despite its therapeutic potential, the insufficient understanding regarding of the receptor's structure Here, we present the structure of GPRC5D in complex with a preclinical-stage single-chain antibody (scFv Our structural analysis reveals that the GPRC5D presents a close resemblance to the typical Class C GPCRs GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- Ep 52 with Dr. Benjamin Myers
signaling mechanisms employed by these atypical 7-transmembrane receptors, combining biochemical and structural begun studying GPCR signaling pathways that operate within the primary cilium, a tiny antenna-shaped structure Prior to that, Ben received his Ph.D. from UCSF in 2008, where he worked with David Julius on the structure
- Ep 74 with Dr. Daniel Wacker
Ray Stevens in 2013 solving several GPCR crystal structures, including that of the first serotonin receptor Bryan Roth where I established GPCR structural biology and learned the ins and outs of molecular pharmacology started my own lab at the Icahn School of Medicine at Mount Sinai in NYC, where I have been working on structure-function
- Gi/o GPCRs drive the formation of actin-rich tunneling nanotubes in cancer cells via a Gβγ/PKCα/FARP1/Cdc42 axis
filopodia-like elongated projections connecting adjacent cells, known as tunneling nanotube (TNT)-like structures Consistent with the established role of Rho small GTPases in the formation of actin-rich projecting structures into the intricate signaling pathways governing the generation of specialized actin-rich elongated structures GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- C5aR2 receptor: The genomic twin of the flamboyant C5aR1
In addition, the structure of C5aR2 and its interaction specificity toward C5a is not structurally elucidated The current study has attempted to close the gap by generating highly refined model structures of C5aR2 GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- Ep 77 with Martin Audet
Martin Audet Structural biologist, pharmacologist, and a professor of pharmacology at Université de Sherbrooke the AudetLab located at the Institute of Pharmacology of Sherbrooke and is an emerging leader in the structural
- Ep 135 with Dr. Katarzyna Marcinkiewicz
Communications, which she joined in April 2020, following three years on the editorial teams of Nature Structural Katarzyna handles submissions in structural biology, biophysics and biochemistry, with a particular focus
- Expanding role of CXCR2 and therapeutic potential of CXCR2 antagonists in inflammatory diseases and cancers
Hence, we provide an overview containing the discovery history, protein structure, signaling pathways , biological functions, structure-activity relationships and clinical significance of CXCR2 antagonists GPCRs in Neuroscience GPCRs in Cardiology, Endocrinology, and Taste GPCRs in Oncology and Immunology Structural
- Ep 40 with Dr. Brian Bender
Brain’s work there primarily focused on structure prediction of GPCRs from sparse experimental data. of California in San Francisco to continue his training as a postdoctoral researcher where he used structural
- Ep 19 with Dr. Fiona Marshall
An expert in GPCR biology, Fiona published the first description of the cloning and structural requirements company, Fiona and her team made considerable breakthroughs in the field of GPCR stabilization and structure-based
- Ep 75 with Vaithish Velazhahan
His Ph.D. work has been focused on understanding the structure and activation of Class D fungal GPCRs developed novel tools and methodologies to study fungal GPCRs which allowed the determination of the first structures