5SYE
Near-atomic resolution cryo-EM reconstruction of doubly bound Taxol- and peloruside-stabilized microtubule
5SYE の概要
| エントリーDOI | 10.2210/pdb5sye/pdb |
| 関連するPDBエントリー | 5SYC 5SYF 5SYG |
| EMDBエントリー | 8320 8321 8322 8323 |
| 分子名称 | Tubulin alpha chain, Tubulin beta chain, GUANOSINE-5'-TRIPHOSPHATE, ... (7 entities in total) |
| 機能のキーワード | taxol, peloruside, microtubule, structural protein |
| 由来する生物種 | Sus scrofa (Pig) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 98898.16 |
| 構造登録者 | |
| 主引用文献 | Kellogg, E.H.,Hejab, N.M.,Howes, S.,Northcote, P.,Miller, J.H.,Diaz, J.F.,Downing, K.H.,Nogales, E. Insights into the Distinct Mechanisms of Action of Taxane and Non-Taxane Microtubule Stabilizers from Cryo-EM Structures. J. Mol. Biol., 429:633-646, 2017 Cited by PubMed Abstract: A number of microtubule (MT)-stabilizing agents (MSAs) have demonstrated or predicted potential as anticancer agents, but a detailed structural basis for their mechanism of action is still lacking. We have obtained high-resolution (3.9-4.2Å) cryo-electron microscopy (cryo-EM) reconstructions of MTs stabilized by the taxane-site binders Taxol and zampanolide, and by peloruside, which targets a distinct, non-taxoid pocket on β-tubulin. We find that each molecule has unique distinct structural effects on the MT lattice structure. Peloruside acts primarily at lateral contacts and has an effect on the "seam" of heterologous interactions, enforcing a conformation more similar to that of homologous (i.e., non-seam) contacts by which it regularizes the MT lattice. In contrast, binding of either Taxol or zampanolide induces MT heterogeneity. In doubly bound MTs, peloruside overrides the heterogeneity induced by Taxol binding. Our structural analysis illustrates distinct mechanisms of these drugs for stabilizing the MT lattice and is of relevance to the possible use of combinations of MSAs to regulate MT activity and improve therapeutic potential. PubMed: 28104363DOI: 10.1016/j.jmb.2017.01.001 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.5 Å) |
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