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Journal: Nature Communications
Article Title: A hotspot phosphorylation site on SHP2 drives oncoprotein activation and drug resistance
doi: 10.1038/s41467-026-70060-8
Figure Lengend Snippet: a Kinase Library prediction heatmap based on the peptide primary sequence of the SHP2 Y62 phosphosite plotted on human kinome evolutionary tree. TK—Tyrosine kinases, CAMK—calcium calmodulin-dependent kinases, TKL—Tyrosine kinase-like, STE- sterile kinases, CK1—Casein Kinase 1. b SFK multi-kinase and selective inhibitors with targets shown, tested here. c , d Immunoblot analysis of ( c ) U-2 OS cells and ( d ) HCC827 cells treated with dasatinib and SU6656 at indicated concentrations, and DMSO. e , f Immunoblot analysis of HCC827 cells treated with ( e ) saracatinib, CH6953755, and PP2, and ( f ) double and triple combinations at indicated concentrations, and DMSO. g Immunoblot analysis of SYF knock out and wildtype MEFs. h In vitro kinase assays with recombinant SRC, YES1, and FYN kinases and recombinant SHP2 WT and SHP2 Y62F . The SHP2 pY542 antibody demonstrated nonspecific binding in the control conditions. All immunoblots are representative of one of the three independent experiments. The unit of molecular weight markers in Western blots is kDa. Source data are provided as source data file.
Article Snippet:
Techniques: Sequencing, Phospho-proteomics, Sterility, Western Blot, Knock-Out, In Vitro, Recombinant, Binding Assay, Control, Molecular Weight