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由植物毒素圆斑弯孢霉毒素引起的ATP合酶抑制和刺激的分子过程。

Molecular processes of inhibition and stimulation of ATP synthase caused by the phytotoxin tentoxin.

作者信息

Meiss Erik, Konno Hiroki, Groth Georg, Hisabori Toru

机构信息

Chemical Resources Laboratory, Tokyo Institute of Technology, Nagatsuta 4259-R1-8, Yokohama 226-8503, Japan.

出版信息

J Biol Chem. 2008 Sep 5;283(36):24594-9. doi: 10.1074/jbc.M802574200. Epub 2008 Jun 25.

Abstract

F1-ATPase is the smallest mechanical motor known. Tentoxin, a cyclic peptide produced by phytopathogenic fungi, inactivates the F1 motor in sensitive plants at nanomolar to micromolar concentrations, whereas higher concentrations surpass the natural activity of the enzyme. Single molecule studies now have clarified the molecular steps involved in both processes. Inactivation delays the dwell time of a single step in the complete 360 degrees turn and results in an asymmetric rotation of the central rotor subunit. In contrast, rotation in the stimulated F1 particle is smooth and accompanied by strongly reduced ADP inhibition. Our study provides for the first time the direct observation of a noncompetitively inhibited state of the enzyme and directly visualizes the regulation of the molecular motor by an external natural compound. In addition, the ADP release step during catalysis was revealed by analysis of the single molecule rotation behavior. Hence, tentoxin is a sophisticated molecular tool to mark and control certain catalytic steps within the reaction pathway of the molecular F1 motor.

摘要

F1 - ATP酶是已知最小的机械马达。抗霉素A,一种由植物致病真菌产生的环肽,在纳摩尔到微摩尔浓度下可使敏感植物中的F1马达失活,而更高浓度则会超过该酶的天然活性。现在单分子研究已经阐明了这两个过程中涉及的分子步骤。失活会延迟中心转子亚基在完整360度旋转中单个步骤的停留时间,并导致其不对称旋转。相比之下,受刺激的F1颗粒中的旋转是平滑的,并且伴随着ADP抑制的大幅降低。我们的研究首次直接观察到该酶的非竞争性抑制状态,并直接可视化了外部天然化合物对分子马达的调节。此外,通过分析单分子旋转行为揭示了催化过程中的ADP释放步骤。因此,抗霉素A是一种精密的分子工具,可标记和控制分子F1马达反应途径中的某些催化步骤。

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