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计算对接揭示了不同植物中 C4 碳输送酶的共同进化。

Computational Docking Reveals Co-Evolution of C4 Carbon Delivery Enzymes in Diverse Plants.

机构信息

State Key Laboratory of Agrobiotechnology, School of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.

出版信息

Int J Mol Sci. 2022 Oct 21;23(20):12688. doi: 10.3390/ijms232012688.

Abstract

Proteins are modular functionalities regulating multiple cellular activities in prokaryotes and eukaryotes. As a consequence of higher plants adapting to arid and thermal conditions, C4 photosynthesis is the carbon fixation process involving multi-enzymes working in a coordinated fashion. However, how these enzymes interact with each other and whether they co-evolve in parallel to maintain interactions in different plants remain elusive to date. Here, we report our findings on the global protein co-evolution relationship and local dynamics of co-varying site shifts in key C4 photosynthetic enzymes. We found that in most of the selected key C4 photosynthetic enzymes, global pairwise co-evolution events exist to form functional couplings. Besides, protein-protein interactions between these enzymes may suggest their unknown functionalities in the carbon delivery process. For PEPC and PPCK regulation pairs, pocket formation at the interactive interface are not necessary for their function. This feature is distinct from another well-known regulation pair in C4 photosynthesis, namely, PPDK and PPDK-RP, where the pockets are necessary. Our findings facilitate the discovery of novel protein regulation types and contribute to expanding our knowledge about C4 photosynthesis.

摘要

蛋白质是调节原核生物和真核生物多种细胞活动的模块功能。由于高等植物适应干旱和热条件,C4 光合作用是涉及多种酶协同工作的碳固定过程。然而,这些酶如何相互作用,以及它们是否平行进化以维持不同植物中的相互作用,至今仍不得而知。在这里,我们报告了我们关于关键 C4 光合作用酶的全局蛋白质共进化关系和共变位点局部动力学的研究结果。我们发现,在大多数选定的关键 C4 光合作用酶中,存在全局成对共进化事件以形成功能耦合。此外,这些酶之间的蛋白质-蛋白质相互作用可能暗示它们在碳传递过程中的未知功能。对于 PEPC 和 PPCK 调节对,相互作用界面上口袋的形成对于它们的功能不是必需的。这一特征与 C4 光合作用中另一个众所周知的调节对 PPDK 和 PPDK-RP 不同,在 PPDK-RP 中,口袋是必需的。我们的发现有助于发现新型蛋白质调节类型,并有助于扩展我们对 C4 光合作用的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f330/9604239/62a0fc17583c/ijms-23-12688-g001.jpg

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