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https://doi.org/10.1007/978-3-642-60015-9nd heteromeric complexes, which in turn dynamically couple with G proteins, and other interacting proteins. Here, we describe a method to simultaneously determine the identity of up to four distinct constituents of GPCR complexes using a combination of sequential bioluminescence resonance energy tra易达到 发表于 2025-3-29 17:12:19
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13 Lectures on Fermat‘s Last Theorem Gα, Gβ, and Gγ subunits, as well as a growing array of regulatory and accessory proteins such as arrestins. G protein-independent β-arrestin recruitment at GPCRs is universally accepted as the canonical interactor system and it has been found to be a powerful tracker of most GPCRs activation. Pharm团结 发表于 2025-3-30 07:59:10
Visionen haben, die Zukunft bewußt gestalteneins in a sample. It is also a powerful methodology to elucidate protein–protein interactions in a sequence-dependent and unbiased manner. G protein-coupled receptors (GPCRs) seldom function in isolation and characterization of proteins present in the receptor complex (or its interactome) is critica