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过硫化修饰和磷酸化对 Sucrose Nonfermenting 1-Related Protein Kinase 2.6 构象的调控:分子动力学模拟的见解。

The Modulation of Sucrose Nonfermenting 1-Related Protein Kinase 2.6 State by Persulfidation and Phosphorylation: Insights from Molecular Dynamics Simulations.

机构信息

College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, China.

Institute of Bast Fiber Crops (IBFC), Chinese Academy of Agricultural Sciences (CAAS), Changsha 410205, China.

出版信息

Int J Mol Sci. 2023 Jul 15;24(14):11512. doi: 10.3390/ijms241411512.

Abstract

SnRK2.6 (SUCROSE NONFERMENTING 1-RELATED PROTEIN KINASE2.6) has been characterized as a molecular switch for the intracellular abscisic acid (ABA) signal-transduction pathway. Normally, SnRK2.6 is kept in an "off" state, forming a binary complex with protein phosphatase type 2Cs (PP2Cs). Upon stressful conditions, SnRK2.6 turns into an "on" state by its release from PP2Cs and then phosphorylation at Ser175. However, how the "on" and "off" states for SnRK2.6 are fine-tuned, thereby controlling the initiation and braking processes of ABA signaling, is still largely unclear. SnRK2.6 activity was tightly regulated through protein post-translational modifications (PTM), such as persulfidation and phosphorylation. Taking advantage of molecular dynamics simulations, our results showed that Cys131/137 persulfidation on SnRK2.6 induces destabilized binding and weakened interactions between SnRK2.6 and HAB1 (HYPERSENSITIVE TO ABA1), an important PP2C family protein. This unfavorable effect on the association of the SnRK2.6-HAB1 complex suggests that persulfidation functions are a positive regulator of ABA signaling initiation. In addition, Ser267 phosphorylation in persulfidated SnRK2.6 renders a stable physical association between SnRK2.6 and HAB1, a key characterization for SnRK2.6 inhibition. Rather than Ser175, HAB1 cannot dephosphorylate Ser267 in SnRK2.6, which implies that the retained phosphorylation status of Ser267 could ensure that the activated SnRK2.6 reforms the binary complex to cease ABA signaling. Taken together, our findings expand current knowledge concerning the regulation of persulfidation and phosphorylation on the state transition of SnRK2.6 and provide insights into the fine-tuned mechanism of ABA signaling.

摘要

SnRK2.6(蔗糖不发酵 1-相关蛋白激酶 2.6)已被鉴定为细胞内脱落酸(ABA)信号转导途径的分子开关。通常情况下,SnRK2.6 处于“关闭”状态,与蛋白磷酸酶 2C 型(PP2C)形成二元复合物。在应激条件下,SnRK2.6 通过从 PP2C 释放并在 Ser175 处磷酸化而变为“开启”状态。然而,SnRK2.6 的“开启”和“关闭”状态如何精细调节,从而控制 ABA 信号的起始和制动过程,在很大程度上仍不清楚。SnRK2.6 活性受到蛋白质翻译后修饰(PTM)的严格调控,如过硫化和磷酸化。利用分子动力学模拟,我们的结果表明,SnRK2.6 上的 Cys131/137 过硫化诱导 SnRK2.6 与 HAB1(ABA1 超敏感)之间的结合不稳定和相互作用减弱,HAB1 是一种重要的 PP2C 家族蛋白。这种对 SnRK2.6-HAB1 复合物结合的不利影响表明,过硫化作用是 ABA 信号起始的正调节剂。此外,过硫化 SnRK2.6 中的 Ser267 磷酸化使 SnRK2.6 与 HAB1 之间形成稳定的物理关联,这是 SnRK2.6 抑制的关键特征。而不是 Ser175,HAB1 不能使 SnRK2.6 中的 Ser267 去磷酸化,这意味着 Ser267 的保留磷酸化状态可以确保激活的 SnRK2.6 重新形成二元复合物以停止 ABA 信号。总之,我们的发现扩展了关于 SnRK2.6 状态转换中过硫化和磷酸化调节的现有知识,并为 ABA 信号的精细调控机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/251f/10380758/86cd69bee520/ijms-24-11512-g001.jpg

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