Center for Vascular Biology Research and Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Mount Desert Island Biological Laboratory, Salisbury Cove, ME, USA.
J Thromb Haemost. 2018 Apr;16(4):734-748. doi: 10.1111/jth.13968. Epub 2018 Mar 12.
Essentials Tissue factor (TF) enhances factor VIIa (FVIIa) activity through structural and dynamic changes. We analyzed conservation of TF-activated FVIIa allosteric networks in extant vertebrate lamprey. Lamprey Tf/FVIIa molecular dynamics show conserved Tf-induced structural/dynamic FVIIa changes. Lamprey Tf activation of FVIIa allosteric networks follows molecular pathways similar to human.
Background Previous studies have provided insight into the molecular basis of human tissue factor (TF) activation of activated factor VII (FVIIa). TF-induced allosteric networks of FVIIa activation have been rationalized through analysis of the dynamic changes and residue connectivities in the human soluble TF (sTF)/FVIIa complex structure during molecular dynamics (MD) simulation. Evolutionary conservation of the molecular mechanisms for TF-induced allosteric FVIIa activation between humans and extant vertebrate jawless fish (lampreys), where blood coagulation emerged more than 500 million years ago, is unknown and of considerable interest. Objective To model the sTf/FVIIa complex from cloned Petromyzon marinus lamprey sequences, and with comparisons to human sTF/FVlla investigate conservation of allosteric mechanisms of FVIIa activity enhancement by soluble TF using MD simulations. Methods Full-length cDNAs of lamprey tf and f7 were cloned and characterized. Comparative models of lamprey sTf/FVIIa complex and free FVIIa were determined based on constructed human sTF/FVIIa complex and free FVIIa models, used in full-atomic MD simulations, and characterized using dynamic network analysis approaches. Results Allosteric paths of correlated motion from Tf contact points in lamprey sTf/FVIIa to the FVIIa active site were determined and quantified, and were found to encompass residue-residue interactions along significantly similar paths compared with human. Conclusions Despite low conservation of residues between lamprey and human proteins, 30% TF and 39% FVII, the structural and protein dynamic effects of TF activation of FVIIa appear conserved and, moreover, present in extant vertebrate proteins from 500 million years ago when TF/FVIIa-initiated extrinsic pathway blood coagulation emerged.
Essentials 组织因子 (TF) 通过结构和动态变化增强因子 VIIa (FVIIa) 的活性。我们分析了现存脊椎动物七鳃鳗中 TF 激活的 FVIIa 变构网络的保守性。七鳃鳗 Tf/FVIIa 分子动力学显示 TF 诱导的 FVIIa 结构/动态变化具有保守性。七鳃鳗 TF 对 FVIIa 变构网络的激活遵循与人类相似的分子途径。
背景 先前的研究提供了对人组织因子 (TF) 激活活化因子 VII (FVIIa) 的分子基础的深入了解。通过分析分子动力学 (MD) 模拟过程中可溶性 TF (sTF)/FVIIa 复合物结构中 FVIIa 激活的动态变化和残基连接性,已经合理化了 TF 诱导的 FVIIa 激活的变构网络。人类和现存无颌脊椎鱼(七鳃鳗)之间 TF 诱导的变构 FVIIa 激活的分子机制的进化保守性尚不清楚,但具有相当大的意义,因为七鳃鳗的血液凝固出现于 5 亿多年前。目的 从克隆的 Petromyzon marinus 七鳃鳗序列中构建 sTf/FVIIa 复合物模型,并与人类 sTF/FVlla 进行比较,通过 MD 模拟研究可溶性 TF 增强 FVIIa 活性的变构机制的保守性。方法 克隆并鉴定了七鳃鳗 tf 和 f7 的全长 cDNA。根据构建的人 sTF/FVIIa 复合物和游离 FVIIa 模型,确定了七鳃鳗 sTf/FVIIa 复合物和游离 FVIIa 的比较模型,并用于全原子 MD 模拟,并用动态网络分析方法进行了表征。结果 确定并量化了七鳃鳗 sTf/FVIIa 中来自 TF 接触点到 FVIIa 活性位点的相关运动的变构途径,并发现与人类相比,这些途径包含沿着非常相似路径的残基-残基相互作用。结论 尽管七鳃鳗和人类蛋白之间的残基保守性低,分别为 30% TF 和 39% FVII,但 TF 对 FVIIa 的激活的结构和蛋白动力学效应似乎是保守的,而且存在于 5 亿年前出现 TF/FVIIa 启动的外源性凝血途径的现存脊椎动物蛋白中。