7M18

HeLa-tubulin in complex with cryptophycin 1

7M18 の概要

• エントリーDOI: 10.2210/pdb7m18/pdb
• 関連するPDBエントリー: 7LXB
• EMDBエントリー: 23569 23615
• 分子名称: Tubulin beta-3 chain, Tubulin alpha-1B chain, Cryptophycin 1, ... (5 entities in total)
• 機能のキーワード: anti-tumor, microtubule, tubulin-rings, polymerization-inhibitor, cell cycle
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 16
• 化学式量合計: 818460.19

構造登録者

Eren, E. (登録日: 2021-03-12, 公開日: 2021-09-08, 最終更新日: 2025-06-04)

主引用文献

Eren, E.,Watts, N.R.,Sackett, D.L.,Wingfield, P.T.
Conformational changes in tubulin upon binding cryptophycin-52 reveal its mechanism of action.
J.Biol.Chem., 297:101138-101138, 2021

PubMed Abstract: Cryptophycin-52 (Cp-52) is potentially the most potent anticancer drug known, with IC values in the low picomolar range, but its binding site on tubulin and mechanism of action are unknown. Here, we have determined the binding site of Cp-52, and its parent compound, cryptophycin-1, on HeLa tubulin, to a resolution of 3.3 Å and 3.4 Å, respectively, by cryo-EM and characterized this binding further by molecular dynamics simulations. The binding site was determined to be located at the tubulin interdimer interface and partially overlap that of maytansine, another cytotoxic tubulin inhibitor. Binding induces curvature both within and between tubulin dimers that is incompatible with the microtubule lattice. Conformational changes occur in both α-tubulin and β-tubulin, particularly in helices H8 and H10, with distinct differences between α and β monomers and between Cp-52-bound and cryptophycin-1-bound tubulin. From these results, we have determined: (i) the mechanism of action of inhibition of both microtubule polymerization and depolymerization, (ii) how the affinity of Cp-52 for tubulin may be enhanced, and (iii) where linkers for targeted delivery can be optimally attached to this molecule.

PubMed: 34461087
DOI: 10.1016/j.jbc.2021.101138

実験手法

ELECTRON MICROSCOPY (3.38 Å)