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Titlebook: G Protein-Coupled Receptors; Immobilization and A Xinfeng Zhao,Qian Li,Jia Quan Book 2023 The Author(s), under exclusive license to Springe

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樓主: duodenum
21#
發(fā)表于 2025-3-25 04:00:33 | 只看該作者
Purification of G Protein-Coupled Receptors,abilization of GPCR using different detergents and styrene-maleic acid–lipid particles. We also highlight the commonly used purification techniques for GPCRs?in literature. Finally, the heterologous expression systems for GPCRs, ranging from bacteria and yeasts to insects, mammalian cells, and ., and the successful purification cases are reviewed.
22#
發(fā)表于 2025-3-25 10:36:31 | 只看該作者
Oriented Immobilization of G Protein-Coupled Receptors,tion, and activity or functional studies. In this chapter, we review the affinity-based non-covalent and site-specific covalent immobilization methods developed for capturing GPCR on solid surfaces. The . and . of each method are also discussed.
23#
發(fā)表于 2025-3-25 12:45:11 | 只看該作者
Key Biochemical Aspects of Drug-Target Interactions,les. In this chapter, we summarize several key biochemical parameters, such as binding affinity and kinetics, dynamic conformational ensembles of drug targets, drug resistance time, rebinding, binding thermodynamics, and ligand efficiency.
24#
發(fā)表于 2025-3-25 16:12:42 | 只看該作者
Book 2023 both non-covalent and covalent manners. The last decade is the dawn of the “post-structural biology” era for G protein-coupled receptor research. As an emerging approach for state-of-the-art immobilization, this book discusses efforts to explore the elegance of naturally-occurring biochemical react
25#
發(fā)表于 2025-3-25 21:28:11 | 只看該作者
26#
發(fā)表于 2025-3-26 01:12:38 | 只看該作者
27#
發(fā)表于 2025-3-26 06:48:08 | 只看該作者
28#
發(fā)表于 2025-3-26 12:27:41 | 只看該作者
29#
發(fā)表于 2025-3-26 13:40:41 | 只看該作者
Immobilized GPCRs in Drug-Receptor Interaction Analysis,f additional examples of new approaches and/or applications for decoding the interaction between drugs and GPCRs have appeared. In this chapter, we present some of the reports using immobilized GPCRs for drug-receptor interaction analysis, including labelled and label-free assays.
30#
發(fā)表于 2025-3-26 18:24:24 | 只看該作者
Immobilized GPCRs in Compound Screening,pound libraries and natural product extracts are the widely used two sources for bioactive compound screening. In this chapter, we aim to review some representative immobilized GPCR-based methods for the discovery of the bioactive compounds targeting the receptors, which may provide insight into the
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