Insights into the inhibitory mechanism of triazole-based small molecules on phosphatidylinositol-4,5-bisphosphate binding pleckstrin homology domain

摘要

Background Phosphatidylinositol 4,5-bisphosphate [PI(4,5)P 2 ] is an important regulator of several cellular processes and a precursor for other second messengers which are involved in cell signaling pathways. Signaling proteins preferably interact with PI(4,5)P 2 through its pleckstrin homology (PH) domain. Efforts are underway to design small molecule-based antagonist, which can specifically inhibit the PI(4,5)P 2 /PH-domain interaction to establish an alternate strategy for the development of drug(s) for phosphoinositide signaling pathways. Methods Surface plasmon resonance, molecular docking, circular dichroism, competitive F?rster resonance energy transfer, isothermal titration calorimetric analyses and liposome pull down assay were used. Results In this study, we employed 1,2,3-triazol-4-yl methanol containing small molecule (CIPs) as antagonists for PI(4,5)P 2 /PH-domain interaction and determined their inhibitory effect by using competitive-surface plasmon resonance analysis (IC 50 ranges from 53 to 159nM for PI(4,5)P 2 /PLCδ1-PH domain binding assay). We also used phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P 3 ], phosphatidylinositol 3,4-bisphosphate [PI(3,4)P 2 ], PI(4,5)P 2 specific PH-domains to determine binding selectivity of the compounds. Various physicochemical analyses showed that the compounds have weak affect on fluidity of the model membrane but, strongly interact with the phospholipase C δ1 (PLCδ1)-PH domains. The 1,2,3-triazol-4-yl methanol moiety and nitro group of the compounds are essential for their exothermic interaction with the PH-domains. Potent compound can efficiently displace PLCδ1-PH domain from plasma membrane to cytosol in A549 cells. Conclusions Overall, our studies demonstrate that these compounds interact with the PIP-binding PH-domains and inhibit their membrane recruitment. General significance These results suggest specific but differential binding of these compounds to the PLCδ1-PH domain and emphasize the role of their structural differences in binding parameters. These triazole-based compounds could be directly used/further developed as potential inhibitor for PH domain-dependent enzyme activity. Graphical abstract Display Omitted Highlights ? The inhibition for PIP/PH domain interaction by small molecules was studied. ? One of the potent compounds selectively inhibits PI(4,5)P 2 /PLCδ1-PH domain interaction. ? Experimental data suggest a possible mechanism of compound binding to PH domain. ? Physiological significance of in vitro inhibition/binding studies was tested under cellular environment.