化学
小分子
几丁质酶
药物发现
计算生物学
组合化学
分子
生物化学
立体化学
酶
有机化学
生物
作者
Wojciech Czestkowski,Łukasz Krzemiński,Michał Piotrowicz,Marzena Mazur,Elżbieta Pluta,Gleb Andryianau,Robert Koralewski,Krzysztof Matyszewski,Sylwia Olejniczak,Michał Kowalski,Katarzyna Lisiecka,Rafał Kozieł,Katarzyna Piwowar,Diana Papiernik,Marcin Nowotny,Agnieszka Napiórkowska-Gromadzka,E. Popowska‐Nowak,Dorota Niedziałek,Grzegorz Wieczorek,Anna Siwińska
标识
DOI:10.1021/acs.jmedchem.3c02255
摘要
Chitinase-3-like-1 (CHI3L1), also known as YKL-40, is a glycoprotein linked to inflammation, fibrosis, and cancer. This study explored CHI3L1's interactions with various oligosaccharides using microscale thermophoresis (MST) and AlphaScreen (AS). These investigations guided the development of high-throughput screening assays to assess interference of small molecules in binding between CHI3L1 and biotinylated small molecules or heparan sulfate-based probes. Small molecule binders of YKL-40 were identified in our chitotriosidase inhibitors library with MST and confirmed through X-ray crystallography. Based on cocrystal structures of potent hit compounds with CHI3L1, small molecule probes 19 and 20 were designed for an AS assay. Structure-based optimization led to compounds 30 and 31 with nanomolar activities and drug-like properties. Additionally, an orthogonal AS assay using biotinylated heparan sulfate as a probe was developed. The compounds' affinity showed a significant correlation in both assays. These screening tools and compounds offer novel avenues for investigating the role of CHI3L1.
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