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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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發(fā)表于 2025-3-21 17:37:22 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱G Protein-Coupled Receptors
副標(biāo)題Immobilization and A
編輯Xinfeng Zhao,Qian Li,Jia Quan
視頻videohttp://file.papertrans.cn/381/380010/380010.mp4
概述Describes progress in functional immobilization of G protein-coupled receptor.Addresses pharmacological parameters in protein-drug interactions.Reviews the applications of protein immobilization
叢書(shū)名稱SpringerBriefs in Molecular Science
圖書(shū)封面Titlebook: G Protein-Coupled Receptors; Immobilization and A Xinfeng Zhao,Qian Li,Jia Quan Book 2023 The Author(s), under exclusive license to Springe
描述This book summarizes the progress made to functional immobilize G protein-coupled receptors (GPCRs) through site-specific or orientated recognition in 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 reactions by using their high specificity and robust reactivity in the complex system, such as site-specific conjugation by covalent recognition between enzymes and their substrates. With the perspective of protein-drug interactions, this book also reviews the applications of protein immobilization, with an emphasis on G protein-coupled receptors, in drug discovery and protein-ligand interaction analysis. In addition, the merits, opportunities and disadvantages are analyzed for different immobilization methods, and a perspective for future directions is presented. Given its scope, this book appeals to a broad readership, particularly researchers engaged in the field of analytical chemistry, bioconjugate chemistry, and chemical biology, and other
出版日期Book 2023
關(guān)鍵詞GPCRs; Oriented immobilization; Drug-ligand interaction;; Natural products; Drug discovery
版次1
doihttps://doi.org/10.1007/978-981-99-0078-7
isbn_softcover978-981-99-0077-0
isbn_ebook978-981-99-0078-7Series ISSN 2191-5407 Series E-ISSN 2191-5415
issn_series 2191-5407
copyrightThe Author(s), under exclusive license to Springer Nature Singapore Pte Ltd. 2023
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發(fā)表于 2025-3-21 20:21:21 | 只看該作者
Xinfeng Zhao,Qian Li,Jia QuanDescribes progress in functional immobilization of G protein-coupled receptor.Addresses pharmacological parameters in protein-drug interactions.Reviews the applications of protein immobilization
板凳
發(fā)表于 2025-3-22 02:30:39 | 只看該作者
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發(fā)表于 2025-3-22 09:27:41 | 只看該作者
,Wordsworth’s ‘Leveling’ Muse in 1798,sirable way to immobilize GPCRs on solid surfaces is oriented immobilization. In this way, the receptors can be optimal in their orientation, conformation, and activity or functional studies. In this chapter, we review the affinity-based non-covalent and site-specific covalent immobilization methods
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發(fā)表于 2025-3-22 14:05:00 | 只看該作者
The Informal Logic of Mathematical Proof,ts in practice. This makes it critical to fundamental research of understanding biological processes and the efforts to develop new therapeutic molecules. In this chapter, we summarize several key biochemical parameters, such as binding affinity and kinetics, dynamic conformational ensembles of drug
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發(fā)表于 2025-3-22 20:58:04 | 只看該作者
https://doi.org/10.1007/978-3-642-73589-9f 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.
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發(fā)表于 2025-3-22 22:47:48 | 只看該作者
180 Keywords Geld- und W?hrungsrechtpound 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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