Travers Timothy, López Cesar A, Agamasu Constance, Hettige Jeevapani J, Messing Simon, García Angel E, Stephen Andrew G, Gnanakaran S
Theoretical Biology and Biophysics Group, Los Alamos, New Mexico; Center for Nonlinear Studies, Los Alamos National Laboratory, Los Alamos, New Mexico.
Theoretical Biology and Biophysics Group, Los Alamos, New Mexico.
Biophys J. 2020 Aug 4;119(3):525-538. doi: 10.1016/j.bpj.2020.06.021. Epub 2020 Jun 27.
CRAF activation requires binding to membrane-anchored and active GTP-bound RAS. Whereas its RAS-binding domain (RBD) contains the main binding interface to the RAS G domain, its cysteine-rich domain (CRD) is responsible for association to anionic lipid-rich membranes. Both RAF domains are connected by a short linker, and it remains unclear if the two domains act independently or if one domain can impact the function of the other. Here, we used a combination of coarse-grained and all-atom molecular dynamics simulations of a CRAF RBD-CRD construct to investigate the dynamics of the RBD when it is tethered to CRD that is anchored to a POPC:POPS model membrane. First, we show that the RBD positioning is very dynamic with a preferential localization near the membrane surface. Next, we show that membrane-localized RBD has its RAS-binding interface mostly inaccessible because of its proximity to the membrane. Several positively charged residues in this interface were identified from simulations as important for driving RBD association to the membrane. Surface plasmon resonance (SPR) measurements confirmed that mutations of these RBD residues reduced the liposome partitioning of RBD-CRD. Last, simulations indicated that the presence of RBD near the membrane led to a local enrichment of anionic lipids that could potentially enhance the membrane affinity of the entire RBD-CRD construct. This was supported by SPR measurements that showed stronger liposome partitioning of RBD-CRD relative to CRD alone. These findings thus suggest that the RBD and CRD have synergistic effects on their membrane dynamics, with CRD bringing RBD closer to the membrane that impacts its accessibility to RAS and with RBD causing local anionic lipid enrichment that enhances the overall affinity between the membrane and RBD-CRD. These mechanisms have potential implications on the order of events of the interactions between RAS and CRAF at the membrane.
CRAF激活需要与膜锚定且结合GTP的活性RAS结合。其RAS结合结构域(RBD)包含与RAS G结构域的主要结合界面,而其富含半胱氨酸的结构域(CRD)负责与富含阴离子脂质的膜结合。两个RAF结构域由一个短连接子相连,目前尚不清楚这两个结构域是独立发挥作用,还是一个结构域会影响另一个结构域的功能。在此,我们结合对CRAF RBD - CRD构建体进行的粗粒度和全原子分子动力学模拟,研究当RBD与锚定在POPC:POPS模型膜上的CRD相连时RBD的动力学。首先,我们表明RBD的定位非常动态,在膜表面附近有优先定位。接下来,我们表明定位在膜上的RBD因其靠近膜,其RAS结合界面大多无法接近。从模拟中确定该界面中的几个带正电残基对于驱动RBD与膜结合很重要。表面等离子体共振(SPR)测量证实,这些RBD残基的突变降低了RBD - CRD在脂质体中的分配。最后,模拟表明膜附近RBD的存在导致阴离子脂质局部富集,这可能会增强整个RBD - CRD构建体对膜的亲和力。SPR测量支持了这一点,该测量表明相对于单独的CRD而言,RBD - CRD在脂质体中的分配更强。因此,这些发现表明RBD和CRD对其膜动力学具有协同作用,CRD使RBD更靠近膜从而影响其与RAS的可及性,而RBD导致局部阴离子脂质富集从而增强膜与RBD - CRD之间的整体亲和力。这些机制对RAS和CRAF在膜上相互作用的事件顺序具有潜在影响。