Francia Francesco, Malferrari Marco, Sacquin-Mora Sophie, Venturoli Giovanni
Laboratorio di Biochimica e Biofisica, Dipartimento di Biologia, Università di Bologna, 40126 Bologna, Italy.
J Phys Chem B. 2009 Jul 30;113(30):10389-98. doi: 10.1021/jp902287y.
The coupling between electron transfer and protein dynamics has been investigated in reaction centers (RCs) from the wild type (wt) and the carotenoid-less strain R26 of the photosynthetic bacterium Rhodobacter sphaeroides. Recombination kinetics between the primary photoreduced quinone acceptor (QA-) and photoxidized donor (P+) have been analyzed at room temperature in RCs incorporated into glassy trehalose matrices of different water/sugar ratios. As previously found in R26 RCs, also in the wt RC, upon matrix dehydration, P+QA- recombination accelerates and becomes broadly distributed, reflecting the inhibition of protein relaxation from the dark-adapted to the light-adapted conformation and the hindrance of interconversion between conformational substates. While in wet trehalose matrices (down to approximately one water per trehalose molecule) P+QA- recombination kinetics are essentially coincident in wt and R26 RCs, more extensive dehydration leads to two-times faster and more distributed kinetics in the carotenoid-containing RC, indicating a stronger inhibition of the internal protein dynamics in the wt RC. Coarse-grained Brownian dynamics simulations performed on the two RC structures reveal a markedly larger flexibility of the R26 RC, showing that a rigid core of residues, close to the quinone acceptors, is specifically softened in the absence of the carotenoid. These experimental and computational results concur to indicate that removal of the carotenoid molecule has long-range effects on protein dynamics and that the structural/dynamical coupling between the protein and the glassy matrix depends strongly upon the local mechanical properties of the protein interior. The data also suggest that the conformational change stabilizing P+QA- is localized around the QA binding pocket.
在光合细菌球形红杆菌的野生型(wt)和无类胡萝卜素菌株R26的反应中心(RCs)中,研究了电子转移与蛋白质动力学之间的耦合。在掺入不同水/糖比的玻璃态海藻糖基质中的反应中心中,于室温下分析了初级光还原醌受体(QA-)与光氧化供体(P+)之间的复合动力学。如先前在R26反应中心中所发现的,在野生型反应中心中也是如此,随着基质脱水,P+QA-复合加速并变得广泛分布,这反映了蛋白质从暗适应构象到光适应构象的弛豫受到抑制,以及构象亚态之间相互转换的阻碍。在湿海藻糖基质中(低至每一个海藻糖分子约一个水分子),野生型和R26反应中心的P+QA-复合动力学基本一致,而更广泛的脱水导致含类胡萝卜素反应中心的动力学快两倍且分布更广泛,表明野生型反应中心内部蛋白质动力学受到更强抑制。对两种反应中心结构进行的粗粒度布朗动力学模拟显示,R26反应中心的灵活性明显更大,表明在没有类胡萝卜素的情况下,靠近醌受体的刚性残基核心会特异性地变软。这些实验和计算结果一致表明,去除类胡萝卜素分子对蛋白质动力学有长期影响,并且蛋白质与玻璃态基质之间的结构/动力学耦合强烈依赖于蛋白质内部的局部力学性质。数据还表明,稳定P+QA-的构象变化定位在QA结合口袋周围。