Department of photothrophic microorganisms - Algatech, Institute of Microbiology, Academy of Sciences of the Czech Republic, Opatovický mlýn, 379 81, Třeboň, Czech Republic,
Photosynth Res. 2013 Oct;116(2-3):465-79. doi: 10.1007/s11120-013-9898-y. Epub 2013 Aug 17.
The mobility of photosynthetic proteins represents an important factor that affects light-energy conversion in photosynthesis. The specific feature of photosynthetic proteins mobility can be currently measured in vivo using advanced microscopic methods, such as fluorescence recovery after photobleaching which allows the direct observation of photosynthetic proteins mobility on a single cell level. The heterogeneous organization of thylakoid membrane proteins results in heterogeneity in protein mobility. The thylakoid membrane contains both, protein-crowded compartments with immobile proteins and fluid areas (less crowded by proteins), allowing restricted diffusion of proteins. This heterogeneity represents an optimal balance as protein crowding is necessary for efficient light-energy conversion, and protein mobility plays an important role in the regulation of photosynthesis. The mobility is required for an optimal light-harvesting process (e.g., during state transitions), and also for transport of proteins during their synthesis or repair. Protein crowding is then a key limiting factor of thylakoid membrane protein mobility; the less thylakoid membranes are crowded by proteins, the higher protein mobility is observed. Mobility of photosynthetic proteins outside the thylakoid membrane (lumen and stroma/cytosol) is less understood. Cyanobacterial phycobilisomes attached to the stromal side of the thylakoid can move relatively fast. Therefore, it seems that stroma with their active enzymes of the Calvin-Benson cycle, are a more fluid compartment in comparison to the rather rigid thylakoid lumen. In conclusion, photosynthetic protein diffusion is generally slower in comparison to similarly sized proteins from other eukaryotic membranes or organelles. Mobility of photosynthetic proteins resembles restricted protein diffusion in bacteria, and has been rationalized by high protein crowding similar to that of thylakoids.
光合作用蛋白的流动性是影响光合作用中光能转化的一个重要因素。目前,可以使用先进的显微镜方法在体内测量光合作用蛋白的流动性,例如光漂白后荧光恢复,这可以直接观察到单细胞水平上光合作用蛋白的流动性。类囊体膜蛋白的异质组织导致蛋白流动性的异质性。类囊体膜既包含蛋白拥挤的无流动性的隔室,也包含蛋白较少的流动区域,允许蛋白的受限扩散。这种异质性代表了一种最佳平衡,因为蛋白拥挤对于高效的光能转化是必要的,而蛋白流动性在光合作用的调节中起着重要作用。流动性是最佳的光捕获过程(例如在状态转换期间)所必需的,也是蛋白质在合成或修复过程中运输所必需的。因此,蛋白拥挤是类囊体膜蛋白流动性的关键限制因素;类囊体膜中蛋白拥挤越少,观察到的蛋白流动性越高。类囊体膜外的光合作用蛋白(腔和基质/胞质溶胶)的流动性了解较少。附着在类囊体基质侧的蓝细菌藻胆体可以相对快速地移动。因此,与相当刚性的类囊体腔相比,基质及其卡尔文-本森循环的活跃酶似乎是一个更具流动性的隔室。总之,与其他真核生物膜或细胞器中的类似大小的蛋白质相比,光合作用蛋白的扩散通常较慢。光合作用蛋白的流动性类似于细菌中受限的蛋白扩散,并通过类似于类囊体的高蛋白拥挤来合理化。