PI(4,5)P 2 Binding Sites in the Ebola Virus Matrix Protein Modulate Assembly and Budding

Abstract Ebola virus (EBOV) causes sever hemorrhagic fever in humans, can cause death in a large percentage of those infected, and still lacks FDA approved treatment options. In this study, we investigated how the essential EBOV protein, VP40, forms stable oligomers to mediate budding and assembly from the host cell plasma membrane. An array of in vitro and cellular assays identified and characterized two lysine rich regions that bind to PI(4,5)P 2 and serve distinct functions through the lipid binding and assembly of the viral matrix layer. We found that when VP40 binds PI(4,5)P 2 , VP40 oligomers become extremely stable and long lived. Together, this work characterizes the molecular basis of PI(4,5)P 2 binding by VP40, which stabilizes formation of VP40 oligomers necessary for viral assembly and budding. Quercetin, a natural product that lowers PI(4,5)P 2 in the plasma membrane, inhibited budding of VP40 VLPs and may inform future treatment strategies against EBOV.