Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut, USA.
Department of Chemistry, University of Connecticut, Storrs, Connecticut, USA.
Protein Sci. 2022 Apr;31(4):850-863. doi: 10.1002/pro.4273. Epub 2022 Jan 22.
The orange carotenoid protein (OCP) is responsible for nonphotochemical quenching (NPQ) in cyanobacteria, a defense mechanism against potentially damaging effects of excess light conditions. This soluble two-domain protein undergoes profound conformational changes upon photoactivation, involving translocation of the ketocarotenoid inside the cavity followed by domain separation. Domain separation is a critical step in the photocycle of OCP because it exposes the N-terminal domain (NTD) to perform quenching of the phycobilisomes. Many details regarding the mechanism and energetics of OCP domain separation remain unknown. In this work, we apply metadynamics to elucidate the protein rearrangements that lead to the active, domain-separated, form of OCP. We find that translocation of the ketocarotenoid canthaxanthin has a profound effect on the energetic landscape and that domain separation only becomes favorable following translocation. We further explore, characterize, and validate the free energy surface (FES) using equilibrium simulations initiated from different states on the FES. Through pathway optimization methods, we characterize the most probable path to domain separation and reveal the barriers along that pathway. We find that the free energy barriers are relatively small (<5 kcal/mol), but the overall estimated kinetic rate is consistent with experimental measurements (>1 ms). Overall, our results provide detailed information on the requirement for canthaxanthin translocation to precede domain separation and an energetically feasible pathway to dissociation.
橙色类胡萝卜素蛋白 (OCP) 负责蓝细菌中的非光化学猝灭 (NPQ),这是一种针对过量光照条件潜在有害影响的防御机制。这种可溶性双结构域蛋白在光激活时会发生深刻的构象变化,涉及到酮类胡萝卜素在腔内部的迁移,随后是结构域分离。结构域分离是 OCP 光循环中的一个关键步骤,因为它使 N 端结构域 (NTD) 暴露出来,从而实现藻胆体的猝灭。关于 OCP 结构域分离的机制和能量学的许多细节仍然未知。在这项工作中,我们应用元动力学来阐明导致 OCP 处于活跃的、结构域分离的形式的蛋白质重排。我们发现,酮类胡萝卜素隐黄质的迁移对能量景观有深远的影响,并且只有在迁移之后,结构域分离才变得有利。我们进一步探索、描述和验证了使用从 FES 上不同状态启动的平衡模拟的自由能表面 (FES)。通过途径优化方法,我们描述了结构域分离的最可能途径,并揭示了该途径上的障碍。我们发现自由能障碍相对较小 (<5 kcal/mol),但总体估计的动力学速率与实验测量值一致 (>1 ms)。总的来说,我们的结果提供了关于隐黄质迁移先于结构域分离的要求的详细信息,并提供了一种能量可行的解离途径。