Gu Xue, Zhang Yalong, Long Dong
MOE Key Laboratory for Cellular Dynamics, School of Life Sciences, University of Science and Technology of China, Hefei, China.
MOE Key Laboratory for Cellular Dynamics, School of Life Sciences, University of Science and Technology of China, Hefei, China; Department of Chemistry, University of Science and Technology of China, Hefei, China.
Biophys J. 2024 Apr 2;123(7):839-846. doi: 10.1016/j.bpj.2024.02.022. Epub 2024 Feb 27.
Ras proteins are important intracellular signaling hubs that can interact with numerous downstream effectors and upstream regulators through their GTPase domains (G-domains) anchored to plasma membranes by the C-terminal hypervariable regions (HVRs). The biological functions of Ras were proposed to be regulated at multiple levels including the intramolecular G-domain-HVR interactions, of which the exact mechanism and specificity are still controversial. Here, we demonstrate that the HVRs, instead of having direct contacts, can weakly perturb the G-domains via an allosteric interaction that is restricted to a ∼20 Å range and highly conserved in the tested Ras isoforms (HRas and KRas4B) and nucleotide-bound states. The origin of this allosteric perturbation has been localized to a short segment (residues 167-171) coinciding with region 1 of HVRs, which exhibits moderate to weak α-helical propensities. A charge-reversal mutation (E168K) of KRas4B in region 1, previously described in the Catalog of Somatic Mutations in Cancer database, was found to induce similar chemical shift perturbations as truncation of the HVR does. Further membrane paramagnetic relaxation enhancement (mPRE) data show that this region 1 mutation alters the membrane orientations of KRas4B and moderately increases the relative population of the signaling-compatible state.
Ras蛋白是重要的细胞内信号枢纽,可通过其C端高变区(HVRs)锚定在质膜上的GTPase结构域(G结构域)与众多下游效应器和上游调节因子相互作用。Ras的生物学功能被认为在多个水平上受到调节,包括分子内G结构域与HVR的相互作用,但其确切机制和特异性仍存在争议。在此,我们证明HVRs并非直接接触,而是通过一种变构相互作用对G结构域产生微弱干扰,这种相互作用局限于约20埃的范围,并且在测试的Ras异构体(HRas和KRas4B)以及核苷酸结合状态中高度保守。这种变构干扰的起源已定位到与HVRs的区域1重合的一个短片段(残基167 - 171),该片段表现出中度至弱的α螺旋倾向。在癌症体细胞突变目录数据库中先前描述的KRas4B区域1中的电荷反转突变(E168K),被发现会诱导与HVR截断类似的化学位移扰动。进一步的膜顺磁弛豫增强(mPRE)数据表明,该区域1突变改变了KRas4B的膜取向,并适度增加了信号兼容状态的相对比例。