Department of Integrative Biology and Pharmacology, McGovern Medical School, University of Texas Health Science Center at Houston, 6431 Fannin St., Houston, Texas, 77030, USA.
Sci Rep. 2019 Feb 14;9(1):2057. doi: 10.1038/s41598-019-38770-w.
Raf kinases are downstream effectors of small GTPase Ras. Mutations in Ras and Raf are associated with a variety of cancers and genetic disorders. Of the three Raf isoforms, cRaf is most frequently involved in tumor initiation by Ras. Cytosolic Raf is auto-inhibited and becomes active upon recruitment to the plasma membrane. Since the catalytic domain of Raf is its kinase domain, we ask the following: does the kinase domain of Raf has potential to interact with membrane and if yes, what role does the membrane interaction play? We present a model of cRaf kinase domain in complex with a heterogeneous membrane bilayer using atomistic molecular dynamics simulation. We show that the kinase domain of cRaf has three distinct membrane-interacting regions: a polybasic motif (R.RKTR) from the regulatory αC-helix, an aromatic/hydrophobic cluster from the N-terminal acidic region (NtA) and positively charged/aromatic cluster from the activation segment (AS). We show that residues from these regions form an extended membrane-interacting surface that resembles the membrane-interacting residues from known membrane-binding domains. Activating phosphorylatable regions (NtA and AS), make direct contact with the membrane whereas R.RKTR forms specific multivalent salt bridges with PA. PA lipids dwell for longer times around the R.RKTR motif. Our results suggest that membrane interaction of monomeric cRaf kinase domain likely orchestrates the Raf activation process and modulates its function. We show that R.RKTR is a hotspot that interacts with membrane when cRaf is monomeric and becomes part of the interface upon Raf dimerization. We propose that in terms of utilizing a specific hotspot to form membrane interaction and dimer formation, both Raf and its upstream binding partner KRas, are similar.
Raf 激酶是小 GTP 酶 Ras 的下游效应物。Ras 和 Raf 的突变与多种癌症和遗传疾病有关。在三种 Raf 同工型中,cRaf 最常通过 Ras 参与肿瘤的起始。细胞质 Raf 被自身抑制,并且在募集到质膜时变得活跃。由于 Raf 的催化结构域是其激酶结构域,我们会问:Raf 的激酶结构域是否有可能与膜相互作用,如果是,膜相互作用起什么作用?我们使用原子分子动力学模拟呈现了一个 cRaf 激酶结构域与异质双层膜复合物的模型。我们表明,cRaf 的激酶结构域有三个不同的膜相互作用区域:来自调节αC-螺旋的多碱性基序(R.RKTR)、来自 N 端酸性区(NtA)的芳香/疏水区和来自激活段(AS)的带正电荷/芳香族簇。我们表明,来自这些区域的残基形成了一个扩展的膜相互作用表面,类似于已知的膜结合结构域的膜相互作用残基。激活可磷酸化区域(NtA 和 AS)与膜直接接触,而 R.RKTR 与 PA 形成特定的多价盐桥。PA 脂质在 R.RKTR 基序周围停留更长时间。我们的结果表明,单体 cRaf 激酶结构域的膜相互作用可能协调 Raf 激活过程并调节其功能。我们表明,当 cRaf 是单体时,R.RKTR 是与膜相互作用的热点,并且在 Raf 二聚化时成为界面的一部分。我们提出,就利用特定的热点形成膜相互作用和二聚体形成而言,Raf 和其上游结合伴侣 KRas 是相似的。