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  • 标题:The mechanism of activation of monomeric B-Raf V600E
  • 本地全文:下载
  • 作者:Ryan C. Maloney ; Mingzhen Zhang ; Hyunbum Jang
  • 期刊名称:Computational and Structural Biotechnology Journal
  • 印刷版ISSN:2001-0370
  • 出版年度:2021
  • 卷号:19
  • 页码:3349-3363
  • DOI:10.1016/j.csbj.2021.06.007
  • 出版社:Computational and Structural Biotechnology Journal
  • 摘要:Oncogenic mutations in the serine/threonine kinase B-Raf, particularly the V600E mutation, are frequent in cancer, making it a major drug target. Although much is known about B-Raf’s active and inactive states, questions remain about the mechanism by which the protein changes between these two states. Here, we utilize molecular dynamics to investigate both wild-type and V600E B-Raf to gain mechanistic insights into the impact of the Val to Glu mutation. The results show that the wild-type and mutant follow similar activation pathways involving an extension of the activation loop and an inward motion of the αC-helix. The V600E mutation, however, destabilizes the inactive state by disrupting hydrophobic interactions present in the wild-type structure while the active state is stabilized through the formation of a salt bridge between Glu600 and Lys507. Additionally, when the activation loop is extended, the αC-helix is able to move between an inward and outward orientation as long as the DFG motif adopts a specific orientation. In that orientation Phe595 rotates away from the αC-helix, allowing the formation of a salt bridge between Lys483 and Glu501. These mechanistic insights have implications for the development of new Raf inhibitors.
  • 关键词:B-Raf ; Oncogene ; Kinase ; Protein structure ; Activation mechanism
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