9H7C
Human Transthyretin in Complex with 4-(1H-imidazol-1-yl)phenol
9H7C の概要
エントリーDOI | 10.2210/pdb9h7c/pdb |
分子名称 | Transthyretin, CALCIUM ION, 4-(1H-IMIDAZOL-1-YL)PHENOL, ... (4 entities in total) |
機能のキーワード | amyloidosis, retinol, thyroxine, rbp, transport protein |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 27955.22 |
構造登録者 | |
主引用文献 | Chen, W. Fragment-based drug discovery for transthyretin kinetic stabilisers using a novel capillary zone electrophoresis method. Plos One, 20:e0323816-e0323816, 2025 Cited by PubMed Abstract: A Capillary Zone Electrophoresis (CZE) fragment screening methodology was developed and applied to the human plasma protein Transthyretin (TTR), normally soluble, but could misfold and aggregate, causing amyloidosis. Termed Free Probe Peak Height Restoration (FPPHR), it monitors changes in the level of free ligand known to bind TTR (the Probe Ligand) in the presence of competing fragments. 129 fragments were screened, 12 of the 16 initial hits (12.4% hit rate) were co-crystallised with TTR, 11 were found at the binding site (92% confirmation rate). Subsequent analogue screens have identified a novel TTR-binding scaffold 4-(3H-pyrazol-4-yl)quinoline and its derived compounds were further studied by crystallography, circular dichroism (CD), isothermal titration calorimetry (ITC) and radiolabelled 125I-Thyroxine displacement assay in neat plasma. Two lead molecules had similar ITC Kd and 125I-Thyroxine displacement IC50 values to that of Tafamidis, adding another potential pipeline for transthyretin amyloidosis. The methodology is reproducible, procedurally simple, automatable, label-free without target immobilisation, non-fluorescence based and site-specific with low false positive rate, which could be applicable to fragment screening of many drug targets. PubMed: 40367241DOI: 10.1371/journal.pone.0323816 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.27 Å) |
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