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Titlebook: GPCR Signalling Complexes – Synthesis, Assembly, Trafficking and Specificity; Denis J. Dupré,Terence E. Hébert,Ralf Jockers Book 2012 Spri

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發(fā)表于 2025-3-21 19:30:43 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱GPCR Signalling Complexes – Synthesis, Assembly, Trafficking and Specificity
編輯Denis J. Dupré,Terence E. Hébert,Ralf Jockers
視頻videohttp://file.papertrans.cn/381/380153/380153.mp4
概述This is the first book addressing specifically the assembly of G protein coupled receptors signaling complexes.Several colors images.Compilations of manuscripts made from experts in the field
叢書名稱Subcellular Biochemistry
圖書封面Titlebook: GPCR Signalling Complexes – Synthesis, Assembly, Trafficking and Specificity;  Denis J. Dupré,Terence E. Hébert,Ralf Jockers Book 2012 Spri
描述Main Question: G protein coupled receptors are involved in highly efficient and specific activation of signalling pathways. How do GPCR signalling complexes get assembled to generate such specificity? In order to answer this question, we need to understand how receptors and their signalling partners are synthesized, folded and quality-controlled in order to generate functional proteins. Then, we need to understand how each partner of the signalling complex is selected to join a complex, and what makes this assembly possible. GPCRs are known to be able to function as oligomers, what drives the assembly into oligomers and what will be the effects of such organization on specificity and efficacy of signal transduction. Once the receptor complexes are assembled, they need to reach different locations in the cell; what drives and controls the trafficking of GPCR signalling complexes. Finally, defects in synthesis, maturation or trafficking can alter functionality of GPCRs signalling complexes; how can we manipulate the system to make it function normally again? Pharmacological chaperones may just be part of the answer to this question.
出版日期Book 2012
關鍵詞Assembly; Chaperone; G protein coupled receptor; Signaling; Trafficking; Receptors
版次1
doihttps://doi.org/10.1007/978-94-007-4765-4
isbn_softcover978-94-017-8099-5
isbn_ebook978-94-007-4765-4Series ISSN 0306-0225 Series E-ISSN 2542-8810
issn_series 0306-0225
copyrightSpringer Science+Business Media Dordrecht 2012
The information of publication is updating

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發(fā)表于 2025-3-21 21:28:33 | 只看該作者
Book 2012 defects in synthesis, maturation or trafficking can alter functionality of GPCRs signalling complexes; how can we manipulate the system to make it function normally again? Pharmacological chaperones may just be part of the answer to this question.
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發(fā)表于 2025-3-22 00:43:29 | 只看該作者
ER-Bound Steps in the Biosynthesis of G Protein-Coupled Receptors,ceptors (but not of receptor subtypes where ligand binding requires a stable fold of the N-tail) is unlikely to establish a stable fold. These segments can cause ER retention when mutated to inappropriately expose hydrophobic peptide patches; to prevent protein aggregation chaperone molecules attach
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Regulatory Processes Governing the Cell Surface Expression of LH and FSH Receptors,xpressed with a misfolded mutant, the misfolded receptor dimerizes with immature wild-type receptor in the ER, causing a dominant-negative effect on cell surface expression of the mature wild-type receptor. Notably, the propensity for homodimerization is not affected by the activation status of the
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,Synthesis and Assembly of G Protein βγ Dimers: Comparison of , and , Studies,ular) studies provide different perspectives of these processes, and a comparison of them can provide insight into both our current level of understanding and directions to be taken in future investigations.
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發(fā)表于 2025-3-22 23:27:00 | 只看該作者
GPCR Signalling Complexes – Synthesis, Assembly, Trafficking and Specificity
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發(fā)表于 2025-3-23 02:25:17 | 只看該作者
I. N. Bronshtein,K. A. Semendyayevceptors (but not of receptor subtypes where ligand binding requires a stable fold of the N-tail) is unlikely to establish a stable fold. These segments can cause ER retention when mutated to inappropriately expose hydrophobic peptide patches; to prevent protein aggregation chaperone molecules attach
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發(fā)表于 2025-3-23 08:40:58 | 只看該作者
https://doi.org/10.1007/978-3-030-39908-5erent partners. In this chapter, we will cover some aspects of the current knowledge about how chaperones are involved in both the formation of GPCR oligomers and in the assembly of the receptors with their signaling complex components.
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