Preprint Article Version 1 Preserved in Portico This version is not peer-reviewed

The Minor Matrix Protein VP24 from Ebola Virus Lacks Direct Lipid-Binding Properties

Version 1 : Received: 16 July 2020 / Approved: 17 July 2020 / Online: 17 July 2020 (06:00:08 CEST)

A peer-reviewed article of this Preprint also exists.

Su, Y.; Stahelin, R.V. The Minor Matrix Protein VP24 from Ebola Virus Lacks Direct Lipid-Binding Properties. Viruses 2020, 12, 869. Su, Y.; Stahelin, R.V. The Minor Matrix Protein VP24 from Ebola Virus Lacks Direct Lipid-Binding Properties. Viruses 2020, 12, 869.

Abstract

Viral protein 24 (VP24) from Ebola virus (EBOV) was first recognized as a minor matrix protein that associates with cellular membranes. However, more recent studies shed light on its roles in inhibiting viral genome transcription and replication, facilitating nucleocapsid assembly and transport, and interfering with immune responses in host cells through downregulation of interferon (IFN)-activated genes. Thus, whether VP24 is a peripheral protein with lipid binding ability for matrix layer recruitment has not been explored. Here we examined the lipid binding ability of VP24 with a number of lipid binding assays. The results indicated that VP24 lacked the ability to associate with lipids tested regardless of VP24 posttranslational modifications. We further demonstrate that the presence of the EBOV major matrix protein VP40 did not promote VP24 membrane association in vitro or in cells. Further, no protein-protein interactions between VP24 and VP40 were detected by co-immunoprecipitation. Confocal imaging and cellular membrane fractionation analyses in human cells suggested VP24 did not specifically localize at the plasma membrane inner leaflet. Overall, we provide evidence that EBOV VP24 is not a lipid binding protein and its presence in the viral matrix layer is likely not dependent on direct lipid interactions.

Keywords

Ebola virus; filovirus; lipid binding; matrix protein; VP24

Subject

Biology and Life Sciences, Virology

Comments (0)

We encourage comments and feedback from a broad range of readers. See criteria for comments and our Diversity statement.

Leave a public comment
Send a private comment to the author(s)
* All users must log in before leaving a comment
Views 0
Downloads 0
Comments 0
Metrics 0


×
Alerts
Notify me about updates to this article or when a peer-reviewed version is published.
We use cookies on our website to ensure you get the best experience.
Read more about our cookies here.