Biomolecular Interactions Part A Methods in Cell Biology Series
1: Measuring the rapid kinetics of receptor-ligand interactions in live cells using NanoBRET
2: Evaluating functional ligand-GPCR interactions in cell-based assays
3: Assays for detecting arrestin interaction with GPCRs
4: BRET-based assay to specifically monitor ß2AR/GRK2 interaction and ß-arrestin2 conformational change upon ßAR stimulation
5: Cannabinoid Receptor CB1 and CB2 Interacting Proteins: Techniques, Progress and Perspectives
6: Purinergic GPCR transmembrane residues involved in ligand recognition and dimerization
7: Nanobodies as Sensors of GPCR Activation and Signaling
8: Confocal and TIRF microscopy based approaches to visualize arrestin trafficking in living cells
9: Strategies for targeting cell surface proteins using multivalent conjugates and chemical biology
10: Identifying Plasmodium falciparum receptor activation using bioluminescence resonance energy transfer (BRET)-based biosensors in HEK293 cells
11: Methods for Binding Analysis of Small GTP-Binding Proteins with their Effectors
12: Protein-protein interactions in the brain: protocol for preparing rodent brain tissue for mass spectrometry-based quantitative- and phospho- proteomics analysis
13: Protein-Protein Interactions at a glance: protocols for the visualization of biomolecular interactions
14: Interactions between Noncoding RNAs as Epigenetic Regulatory Mechanisms in Cardiovascular Diseases
- Provides the authority and expertise of leading contributors from an international board of authors
- Presents the latest release in the Methods in Cell Biology series
- Updated release includes the latest information on biomolecular interactions instead of protein-protein interactions
Date de parution : 10-2021
Ouvrage de 368 p.
15.2x22.8 cm
Thème de Biomolecular Interactions Part A :
Mots-clés :
3D representation; Adenosine receptors; Antibody; Antibody-drug conjugate; Arrestin; Binding; Bioluminescence resonance energy transfer; Biosensor; Bispecific; Brain; BRET; Cannabinoid; Cardiovascular disease; CB1; CB2; Cell signaling; Cell-based activity assay; Cellular signaling; Chemical biology; Chimera; Circular noncoding RNA; Co-immunoprecipitation; Confocal microscopy; Dimer; Effectors; Endosomes; G protein-coupled receptor (GPCR); G protein-coupled receptor kinase; G protein-coupled receptors (GPCRs); Gene regulation; GPCR; GPCR activation; GPCRs; Heteromer; Interaction; IP1 assay; Kinetics; Ligand-induced activation; Live cells; Long noncoding RNA; Mass spectrometry; microRNA; Molecular interactions; Multimerization; Nanobody; NanoBRET; Neurodegeneration; Nucleotides; P2Y receptors; Plasmodium; Post-translational modifications; Protein; Protein interface; Protein photorealism; Protein-protein interaction; Protein-protein interactions; Proteomics; Receptor; signaling; Signaling; Small GTPase; Surface; TIRF microscopy; Trafficking; Unmodified receptor; VHH; X-ray crystallography; Yeast two-hybrid; ß-adrenergic receptor; ß-arrestin