Zhang Yubo, Ding Yi
State Key Laboratory of Hybrid Rice, Department of Genetics, College of Life Sciences, Wuhan University, Wuhan, 430072, People's Republic of China.
BMC Bioinformatics. 2016 Jan 12;17:28. doi: 10.1186/s12859-016-0877-0.
Rice (Oryza sativa L.) is one of the most important cereal crops in the world and its yield is closely related to the photosynthesis efficiency. The chloroplast stromal ridge complex consisting of PsaC-PsaD-PsaE plays an important role in plant photosynthesis, which has been a subject of many studies. Till now, the recognition mechanism between PsaC and PsaD in rice is still not fully understood.
Here, we present the interaction features of OsPsaC and OsPsaD by molecular dynamics simulations and bioinformatics. Firstly, we identified interacting residues in the OsPsaC-OsPsaD complex during simulations. Significantly, important hydrogen bonds were observed in residue pairs R19-E103, D47-K62, R53-E63, Y81-R20, Y81-R61 and L26-V105. Free energy calculations suggested two salt bridges R19-E103 and D47-K62 were essential to maintain the OsPsaC-OsPsaD interaction. Supportively, electrostatic potentials surfaces of OsPsaD exhibited electrostatic attraction helped to stabilize the residue pairs R19-E103 and D47-K62. In particular, the importance of R19 was further verified by two 500 ns CG-MD simulations. Secondly, this study compared the stromal ridge complex in rice with that in other organisms. Notably, alignments of amino acids showed these two salt bridges R19-E103 and D47-K62 also existed in other organisms. Electrostatic potentials surfaces and X-ray structural analysis strongly suggested the stromal ridge complex in other organisms adopted a similar and general recognition mechanism.
These results together provided structure basis and dynamics behavior to understand recognition and assembly of the stromal ridge complex in rice.
水稻(Oryza sativa L.)是世界上最重要的谷类作物之一,其产量与光合作用效率密切相关。由PsaC - PsaD - PsaE组成的叶绿体基质脊复合物在植物光合作用中起重要作用,一直是众多研究的对象。到目前为止,水稻中PsaC和PsaD之间的识别机制仍未完全了解。
在此,我们通过分子动力学模拟和生物信息学展示了OsPsaC和OsPsaD的相互作用特征。首先,我们在模拟过程中确定了OsPsaC - OsPsaD复合物中的相互作用残基。值得注意的是,在残基对R19 - E103、D47 - K62、R53 - E63、Y81 - R20、Y81 - R61和L26 - V105中观察到重要的氢键。自由能计算表明两个盐桥R19 - E103和D47 - K62对于维持OsPsaC - OsPsaD相互作用至关重要。支持性的是,OsPsaD的静电势表面表现出静电吸引力,有助于稳定残基对R19 - E103和D47 - K62。特别是,通过两个500 ns的粗粒度分子动力学模拟进一步验证了R19的重要性。其次,本研究将水稻中的基质脊复合物与其他生物体中的进行了比较。值得注意的是,氨基酸序列比对表明这两个盐桥R19 - E103和D47 - K62在其他生物体中也存在。静电势表面和X射线结构分析强烈表明其他生物体中的基质脊复合物采用了类似的通用识别机制。
这些结果共同为理解水稻中基质脊复合物的识别和组装提供了结构基础和动力学行为。