Josef Holub,Adéla Jílková,Carina Lemke,Lorenzo Cianni,Petra Spiwoková,Martin Horn,Christian Breuer,Adrian Leontovyč,Jiří Brynda,Helena Mertlíková-Kaiserová,Marta Chanová,Fernanda Dos Reis Rocho,Carlos A Montanari,Nelly El-Sakkary,Conor R Caffrey,Michael Gütschow,Drahomír Hnyk,Michael Mareš,Jindřich Fanfrlík
{"title":"胖还是扁?偶极矩矢量对芳香标签与大分子间非共价相互作用的影响。","authors":"Josef Holub,Adéla Jílková,Carina Lemke,Lorenzo Cianni,Petra Spiwoková,Martin Horn,Christian Breuer,Adrian Leontovyč,Jiří Brynda,Helena Mertlíková-Kaiserová,Marta Chanová,Fernanda Dos Reis Rocho,Carlos A Montanari,Nelly El-Sakkary,Conor R Caffrey,Michael Gütschow,Drahomír Hnyk,Michael Mareš,Jindřich Fanfrlík","doi":"10.1039/d5qi01546d","DOIUrl":null,"url":null,"abstract":"The closo-1,2-C2B10H12 carborane is a recognized 3D aromatic icosahedral building block, with an electron distribution governed by the outer hydridic BH and acidic CH vertices. We attached the carborane cage to a peptidomimetic scaffold to generate an active-site inhibitor of SmCB1, a protease drug target in the Schistosoma pathogen. The carborane-tagged compound exhibited superior inhibitor affinity and bioactivity compared to its conventional 2D aromatic phenyl analog. Quantum mechanical computations, based on the crystal structure of the protease-inhibitor complex, revealed that the carborane tag contributed to inhibitor binding not only through nonpolar interactions but also via a key hydrogen bond between its CH vertex and a negatively charged residue in the binding site. This interaction, driven by the large dipole moment of the carborane cage, resulted in a more favorable energy contribution than that of the phenyl group in the 2D analog. The carborane pharmacophore boosted affinity for SmCB1 and conferred specific anti-schistosomal activity, highlighting its potential in protein ligand design.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"56 1","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fat or flat? The impact of dipole moment vectors on non-covalent interactions between aromatic tags and macromolecules.\",\"authors\":\"Josef Holub,Adéla Jílková,Carina Lemke,Lorenzo Cianni,Petra Spiwoková,Martin Horn,Christian Breuer,Adrian Leontovyč,Jiří Brynda,Helena Mertlíková-Kaiserová,Marta Chanová,Fernanda Dos Reis Rocho,Carlos A Montanari,Nelly El-Sakkary,Conor R Caffrey,Michael Gütschow,Drahomír Hnyk,Michael Mareš,Jindřich Fanfrlík\",\"doi\":\"10.1039/d5qi01546d\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The closo-1,2-C2B10H12 carborane is a recognized 3D aromatic icosahedral building block, with an electron distribution governed by the outer hydridic BH and acidic CH vertices. We attached the carborane cage to a peptidomimetic scaffold to generate an active-site inhibitor of SmCB1, a protease drug target in the Schistosoma pathogen. The carborane-tagged compound exhibited superior inhibitor affinity and bioactivity compared to its conventional 2D aromatic phenyl analog. Quantum mechanical computations, based on the crystal structure of the protease-inhibitor complex, revealed that the carborane tag contributed to inhibitor binding not only through nonpolar interactions but also via a key hydrogen bond between its CH vertex and a negatively charged residue in the binding site. This interaction, driven by the large dipole moment of the carborane cage, resulted in a more favorable energy contribution than that of the phenyl group in the 2D analog. The carborane pharmacophore boosted affinity for SmCB1 and conferred specific anti-schistosomal activity, highlighting its potential in protein ligand design.\",\"PeriodicalId\":79,\"journal\":{\"name\":\"Inorganic Chemistry Frontiers\",\"volume\":\"56 1\",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2025-10-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5qi01546d\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi01546d","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Fat or flat? The impact of dipole moment vectors on non-covalent interactions between aromatic tags and macromolecules.
The closo-1,2-C2B10H12 carborane is a recognized 3D aromatic icosahedral building block, with an electron distribution governed by the outer hydridic BH and acidic CH vertices. We attached the carborane cage to a peptidomimetic scaffold to generate an active-site inhibitor of SmCB1, a protease drug target in the Schistosoma pathogen. The carborane-tagged compound exhibited superior inhibitor affinity and bioactivity compared to its conventional 2D aromatic phenyl analog. Quantum mechanical computations, based on the crystal structure of the protease-inhibitor complex, revealed that the carborane tag contributed to inhibitor binding not only through nonpolar interactions but also via a key hydrogen bond between its CH vertex and a negatively charged residue in the binding site. This interaction, driven by the large dipole moment of the carborane cage, resulted in a more favorable energy contribution than that of the phenyl group in the 2D analog. The carborane pharmacophore boosted affinity for SmCB1 and conferred specific anti-schistosomal activity, highlighting its potential in protein ligand design.