4lf3

Inhibitory Mechanism of an Allosteric Antibody Targeting the Glucagon Receptor

spinqualitylabelsall models 4lf3, resolution 2.73Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 4lf3 is a 6 chain structure with sequence from Human and Lk3 transgenic mice. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Related: 4ers, 4lex Gene: Anti GCGR mAb (LK3 transgenic mice), GCGR (HUMAN) Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [GLR_HUMAN] This is a receptor for glucagon which plays a central role in regulating the level of blood glucose by controlling the rate of hepatic glucose production and insulin secretion. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase and also a phosphatidylinositol-calcium second messenger system. Publication Abstract from PubMed Elevated glucagon levels and increased hepatic glucagon receptor (GCGR) signaling contribute to hyperglycemia in type 2 diabetes. We have identified a monoclonal antibody that inhibits GCGR, a class-B G-protein coupled receptor (GPCR), through a unique allosteric mechanism. Binding of this antibody to two distinct sites that lie outside the glucagon binding cleft mediate receptor inhibition. One site consists of a patch of residues that are surface exposed on the face of the extracellular domain (ECD) opposite the ligand-binding cleft while the second binding site consists of residues in the alphaA helix of the ECD. A docking model suggests that the antibody does not occlude the ligand-binding cleft. We solved the crystal structure of GCGR ECD containing a naturally occurring G40S mutation and found a shift in the register of the alphaA helix that prevents antibody binding. We also found that alterations in the alphaA helix impact the normal function of GCGR. We present a model for the allosteric inhibition of GCGR by a monoclonal antibody that may form the basis for the development of allosteric modulators for the treatment of diabetes and other class-B GPCR-related diseases. Inhibitory mechanism of an allosteric antibody targeting the glucagon receptor.,Mukund S, Shang Y, Clarke HJ, Madjidi A, Corn JE, Kates L, Kolumam G, Chiang V, Luis E, Murray J, Zhang Y, Hotzel I, Koth CM, Allan BB J Biol Chem. 2013 Nov 4. PMID:24189067 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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