MARTX毒素エフェクタによるRho GTPasesのNε-脂肪アサイル化
Yan Zhou1, Chunfeng Huang1, Li Yin1
1Life Sciences Institute and Innovation Center for Cell Signaling Network, Zhejiang University, Hangzhou, Zhejiang 310058, China.
まとめ
MARTX毒素と呼ばれるバクテリアの毒素は 宿主細胞にエフェクタドメインを放出します 1つのドメインであるRIDは脂肪アシルトランスフェラーゼとして作用し,Rho GTPasesを改変し,宿主細胞のシグナル伝達を妨害する.
科学分野:
- 微生物学
- 分子生物学
- 生物化学
背景:
- 多機能自動処理の毒素 (MARTX) は,細菌の病原体の中で一般的です.
- これらの毒素は 宿主の信号伝達経路を 調節するエフェクタドメインに 分裂します
研究 の 目的:
- MARTX毒素のRho GTPase不活性化領域 (RID) の機能を調査する.
- RID が宿主アクチン細胞骨格を破壊し,細胞の丸くするメカニズムを解明する.
主な方法:
- RIDの酵素活性を決定する生化学的測定
- ホスト細胞におけるRho GTPase変異の分析
主要な成果:
- RIDはNε脂肪酸アシルトランスフェラーゼとして機能する.
- RIDは,Rho GTPasesのC端の多塩基領域におけるライシン残基を共性的に変化させる.
- Rho GTPasesの脂肪酸化により,その活性が抑制され,下流信号伝達が妨げられます.
結論:
- RIDは哺乳類のタンパク質のライシンNε-脂肪アシレーションを媒介する.
- MARTX毒素は,N-脂肪アシルトランスフェラーゼ活性を持つ新しい細菌毒素の家族を表しています.
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