6TXV
A25T Transthyretin structure in complex with Tolcalpone
6TXV の概要
| エントリーDOI | 10.2210/pdb6txv/pdb |
| 分子名称 | Transthyretin, Tolcapone (3 entities in total) |
| 機能のキーワード | drug repositioning, tolcapone, leptomeningeal amyloidosis, 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 | 26012.97 |
| 構造登録者 | Varejao, N.,Reverter, D.,Pinheiro, F.,Pallares, I.,Ventura, S. (登録日: 2020-01-14, 公開日: 2020-05-13, 最終更新日: 2024-01-24) |
| 主引用文献 | Pinheiro, F.,Varejao, N.,Esperante, S.,Santos, J.,Velazquez-Campoy, A.,Reverter, D.,Pallares, I.,Ventura, S. Tolcapone, a potent aggregation inhibitor for the treatment of familial leptomeningeal amyloidosis. Febs J., 288:310-324, 2021 Cited by PubMed Abstract: Hereditary transthyretin amyloidosis (ATTR) is a disease characterized by the extracellular deposition of transthyretin (TTR) amyloid fibrils. Highly destabilizing TTR mutations cause leptomeningeal amyloidosis, a rare, but fatal, disorder in which TTR aggregates in the brain. The disease remains intractable, since liver transplantation, the reference therapy for systemic ATTR, does not stop mutant TTR production in the brain. In addition, despite current pharmacological strategies have shown to be effective against in vivo TTR aggregation by stabilizing the tetramer native structure and precluding its dissociation, they display low brain permeability. Recently, we have repurposed tolcapone as a molecule to treat systemic ATTR. Crystal structures and biophysical analysis converge to demonstrate that tolcapone binds with high affinity and specificity to three unstable leptomeningeal TTR variants, stabilizing them and, consequently, inhibiting their aggregation. Because tolcapone is an FDA-approved drug that crosses the blood-brain barrier, our results suggest that it can translate into a first disease-modifying therapy for leptomeningeal amyloidosis. DATABASES: PDB codes for A25T-TTR, V30G-TTR, and Y114C-TTR bound to tolcapone are 6TXV, 6TXW, and 6XTK, respectively. PubMed: 32324953DOI: 10.1111/febs.15339 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.6 Å) |
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