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K-Ras bound to a small molecule to prevent activation by Cat. # SOS1

GDP-K-Ras complexed to a phenol moiety (small arrow head; PDB code 4EPT; 2-hydroxyphenyl)(pyrrolidin-1-yl)methanethione) as described in Sun Q. et al. 2012. Discovery of small molecules that bind to K-Ras and inhibit Sos-mediated activation. Angew Chem. Int. Ed. Engl. 51, 6140–6143.

Recently, Sakamoto et al. discovered novel peptide inhibitors of the G12D mutant K-Ras GTPase. Of the three Ras isoforms (H-, K-, and N-), K-Ras is considered the most relevant anti-cancer drug target as K-Ras mutations underlie 86% of Ras-linked cancers with 83% of K-Ras mutations at the G12 residue. Development of K-Ras-targeting anti-cancer drugs remains elusive due to the paucity of small, druggable pockets on the GTPase’s surface and picomolar binding affinity between K-Ras and GDP/GTP nucleotides. Here, the authors screened random peptide libraries displayed on T7 phage against recombinant G12D K-Ras in the presence of GDP to identify selective G12D K-Ras inhibitors. Sequence optimization produced a selective G12D K-Ras inhibitor (IC50, 1.6 nM) in a SOS1-mediated GDP/GTP exchange assay. At 30 mM, this inhibitor also reduced proliferation and downstream K-Ras signaling in cancer cells. While less than optimal cell membrane permeability and loss of activity under reducing conditions were shortcomings with this peptide, the discovery of selective G12D K-Ras inhibitors provides a blueprint for the design of future, clinically-relevant K-Ras inhibitors. Cytoskeleton’s SOS1 exchange domain protein (564-1049 amino acids; Cat.# CS-SOS1) was used in the GDP/GTP exchange assay to confirm inhibition of G12D K-Ras activation using BODIPY-FL-GDP.

 

Link to citation: 

Sakamoto K. et al. 2017. K-Ras(G12D)-selective inhibitory peptides generated by random peptide T7 phage display technology. Biochem. Biophys. Res. Commun. DOI: 10.1016/j.bbrc.2017.01.147.

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alex castellanos