Cefotetan-bound human RKIP involves in Ras/Raf1/MEK/ERK signaling pathway  

作　　者：Chenyun Guo Hao Xu Yu Zhou Zhihua Wu Bin Jiang Hanyu Chen Donghai Lin 

机构地区：[1]Key Laboratory for Chemical Biology of Fujian Province,College of Chemistry and Chemical Engineering,Xiamen University,Xiamen 361005,China [2]Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province,Xiamen 361005,China [3]State Key Laboratory of Cellular Stress Biology,School of Life Sciences,Xiamen University,Xiamen 361005,China

出　　处：《Acta Biochimica et Biophysica Sinica》2022年第12期1917-1923,共7页生物化学与生物物理学报（英文版）

基　　金：supported by the grants from the Natural Science Foundation of China(No.31470034);the Natural Science Foundation of Fujian Province(No.2020J01022);the Joint Funds for the Innovation of Science and Technology,Fujian Province(No.2018Y9100);the Open Research Fund of State Key Laboratory of Cellular Stress Biology,Xiamen University(No.SKLCSB2020KF002).

摘　　要：Cefotetan is widely used to treat bacterial infections in the clinic owing to its broad spectrum of antibacterial activity.In the present study,we demonstrate that cefotetan can bind to the conserved ligand-binding pocket of human Raf1 kinase inhibitory protein(hRKIP),which acts as a negative regulator of the Ras/Raf1/MEK/ERK signaling pathway.The cefotetan-bound hRKIP adopts a rigid structure with insufficient space for binding Raf1 kinase,thereby reliving the inhibitory activity of hRKIP in the Ras/Raf1/MEK/ERK signaling pathway and enhancing the phosphorylation level of ERK.Both NMR titration and molecular docking approaches show that several residues(P74,Y81,W84,P111,P112,K113,S142,G143,D144,W173,P178,Y181 and L184)play crucial roles in hRKIP binding cefotetan.NMR dynamics analysis reveals that the binding of cefotetan with hRKIP promotes ps-ns internal motion but reducesμs-ms conformational exchange for residues in the cefotetan-binding pocket of hRKIP.Our results not only disclose the structural basis of cefotetan upregulating the Ras/Raf1/MEK/ERK signaling pathway but also benefit developing novel drugs against diseases caused by the impaired Ras/Raf1/MEK/ERK pathway.

关 键 词：CEFOTETAN ERK phosphorylation hRKIP NMR BLI 

分 类 号：Q5[生物学—生物化学]