Download Adhesion G Protein-coupled Receptors: Molecular, by Tobias Langenhan, Torsten Schöneberg PDF

By Tobias Langenhan, Torsten Schöneberg

Latest study on Adhesion GPCRs has unearthed brilliant revelations in regards to the occasions that govern the sign transduction of those receptor molecules and the mobile and organ necessities for those indications. unforeseen and remarkable findings recommend that Adhesion GPCRs represent a bunch of receptors that experience mechanical stimuli and transcode them into metabotropic indications in the course of the motion of a unique activation paradigm. Interdisciplinary efforts transcending many parts of biomedical study together with pharmacology, body structure, genetics, mobile biology, structural biology, biochemistry and bioinformatics have been essential to unveil those basic homes. The clinical leaders within the box that carried this learn attempt have teamed up right here to supply a complete assessment of our present realizing, how Adhesion GPCRs sign and the way those receptors form organ constitution and function.

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Additional resources for Adhesion G Protein-coupled Receptors: Molecular, Physiological and Pharmacological Principles in Health and Disease

Sample text

Collagen III and major cross-linking enzyme transglutaminase 2 (TG2) have been identified as binding partners for ADGRG1 [121, 122]. Collagen III binds in the NTF region range 27–160 aa, and, noteworthy, glycosylation is not a prerequisite for interaction to take place [123]. TG2 binds between 108 and 177 aa in the NTF of ADGRG1 [121, 124]. It is not clear whether collagen III and TG2 can bind simultaneously to the NTF. , corticosteroid beclomethasone dipropionate) has been reported [125]. ADGRG6 interacts with collagen IV and laminin-211.

Collagen III binds in the NTF region range 27–160 aa, and, noteworthy, glycosylation is not a prerequisite for interaction to take place [123]. TG2 binds between 108 and 177 aa in the NTF of ADGRG1 [121, 124]. It is not clear whether collagen III and TG2 can bind simultaneously to the NTF. , corticosteroid beclomethasone dipropionate) has been reported [125]. ADGRG6 interacts with collagen IV and laminin-211. Collagen IV binds to the CUB and PTX domains [126]. Laminin-211 has been shown to interact with a novel laminin-binding domain (446–807 aa) in the ADGRG6 NTF and thereby prevents Stachel-induced receptor activation [127].

The HBD of ADGRA2 and ADGRA3 is most closely related to the HBD of ADGRB3 (BAI3) receptor [85]. Classification, Nomenclature, and Structural Aspects of Adhesion GPCRs 29 ADGRA2 has a GPS site, but is predicted to be non-cleavable. Interestingly, shed NTF of this receptor could be detected in cell culture medium. This is caused by a cleavage site in the NTF that is an interaction point for thrombin-induced shedding promoted by cell surface protein disulfide isomerase [88]. The RGD motif in ADGRA2 can bind αvβ3 integrin [86].

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