9xmm

Cryo-EM structure of Integrin alpha V beta 6 complex with a bicyclic inhibitory peptide

spinqualitylabelsall models 9xmm, resolution 2.88Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 9xmm is a 3 chain structure with sequence from Homo sapiens and Synthetic construct. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: Electron Microscopy, Resolution 2.88Å Ligands: BMA, CA, CHG, MAN, MN, NAG Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function ITAV_HUMAN The alpha-V integrins are receptors for vitronectin, cytotactin, fibronectin, fibrinogen, laminin, matrix metalloproteinase-2, osteopontin, osteomodulin, prothrombin, thrombospondin and vWF. They recognize the sequence R-G-D in a wide array of ligands. In case of HIV-1 infection, the interaction with extracellular viral Tat protein seems to enhance angiogenesis in Kaposi's sarcoma lesions. Publication Abstract from PubMed Bicyclic peptides are promising candidates for peptide-drug conjugates due to their structural rigidity and high target specificity. Recently, it became more apparent that some peptides form nonclassical conformational isomers, termed ansamers. These conformational isomers designated as P(ansa) and M(ansa) are non-interconvertible and separable, thus broaden the chemical space of the peptide template. In this study, we incorporated the RGD motif into a bicyclic peptide and systematically assessed the inhibitory activities of the P(ansa) and M(ansa) isomers against various integrins. The molecule 10-M(ansa) exhibited high selectivity and potent inhibitory activity against the alphavbeta6 integrin, whereas 10-P(ansa), its conformational counterpart, lacked such activity. The cryo-EM structure of alphavbeta6 bound to 10-M(ansa) shows, that it adopts a conformation with the cyclohexane sidechain of the amino acid Chg engaging in hydrophobic interactions with Ile183 and the disulfide bond within the beta6 SDL2 loop. Compared to the linear peptide A20FMDV, a broadly applied alphavbeta6 inhibitor, 10-M(ansa) displays faster cellular internalization and also sustains prolonged enrichment within tumor tissues. Moreover, employing 10-M(ansa) a designed toxin-drug conjugate exhibits remarkable tumor-suppressing effects in vivo. These findings reveal how conformational isomers of ansamers affect biological activity-and highlight their potential for the identification of new bioactive molecules. Ansamer-Controlled Bicyclic Peptides as Integrin alphavbeta6 Targeting Agents.,Yang H, Dong W, An Y, He Z, Pan H, Pan W, Tan J, Sun J, Shen C, Su W, Wang J, Sussmuth RD, Yao G Angew Chem Int Ed Engl. 2026 Apr 5:e1254428. doi: 10.1002/anie.1254428. PMID:41937119 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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