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ADP-核糖基化因子-1(Arf1)与 Arno 鸟嘌呤核苷酸交换因子的 Sec7 结构域之间的相互作用动力学,变构因子的调节作用,以及非竞争性抑制剂布雷菲德菌素 A。

Kinetics of interaction between ADP-ribosylation factor-1 (Arf1) and the Sec7 domain of Arno guanine nucleotide exchange factor, modulation by allosteric factors, and the uncompetitive inhibitor brefeldin A.

机构信息

Institut des Biomolécules Max Mousseron, IBMM, UMR 5247 CNRS-Universités Montpellier 1 et 2 Faculté de Pharmacie, 15 avenue Charles Flahault BP14491, 34093 Montpellier cedex 5, France.

出版信息

J Biol Chem. 2013 Feb 15;288(7):4659-72. doi: 10.1074/jbc.M112.391748. Epub 2012 Dec 19.

Abstract

The GDP/GTP nucleotide exchange of Arf1 is catalyzed by nucleotide exchange factors (GEF), such as Arno, which act through their catalytic Sec7 domain. This exchange is a complex mechanism that undergoes conformational changes and intermediate complex species involving several allosteric partners such as nucleotides, Mg(2+), and Sec7 domains. Using a surface plasmon resonance approach, we characterized the kinetic binding parameters for various intermediate complexes. We first confirmed that both GDP and GTP counteract equivalently to the free-nucleotide binary Arf1-Arno complex stability and revealed that Mg(2+) potentiates by a factor of 2 the allosteric effect of GDP. Then we explored the uncompetitive inhibitory mechanism of brefeldin A (BFA) that conducts to an abortive pentameric Arf1-Mg(2+)-GDP-BFA-Sec7 complex. With BFA, the association rate of the abortive complex is drastically reduced by a factor of 42, and by contrast, the 15-fold decrease of the dissociation rate concurs to stabilize the pentameric complex. These specific kinetic signatures have allowed distinguishing the level and nature as well as the fate in real time of formed complexes according to experimental conditions. Thus, we showed that in the presence of GDP, the BFA-resistant Sec7 domain of Arno can also associate to form a pentameric complex, which suggests that the uncompetitive inhibition by BFA and the nucleotide allosteric effect combine to stabilize such abortive complex.

摘要

Arf1 的 GDP/GTP 核苷酸交换由核苷酸交换因子 (GEF) 催化,例如 Arno,其通过其催化 Sec7 结构域起作用。这种交换是一种复杂的机制,经历构象变化和涉及几个变构伴侣(如核苷酸、Mg(2+)和 Sec7 结构域)的中间复合物物种。使用表面等离子体共振方法,我们表征了各种中间复合物的动力学结合参数。我们首先证实 GDP 和 GTP 等效地与游离核苷酸二元 Arf1-Arno 复合物的稳定性相互作用,并揭示了 Mg(2+)将变构效应增强了 2 倍。然后,我们探索了布雷菲德菌素 A (BFA) 的非竞争性抑制机制,该机制导致无效的五聚体 Arf1-Mg(2+)-GDP-BFA-Sec7 复合物。有了 BFA,无效复合物的缔合速率急剧降低了 42 倍,相比之下,解离速率的 15 倍下降有助于稳定五聚体复合物。这些特定的动力学特征允许根据实验条件实时区分形成复合物的水平、性质和命运。因此,我们表明,在 GDP 的存在下,Arno 的 BFA 抗性 Sec7 结构域也可以与之结合形成五聚体复合物,这表明 BFA 的非竞争性抑制和核苷酸变构效应结合在一起稳定了这种无效复合物。

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