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The Rotavirus NSP4 Viroporin Domain is a Calcium-conducting Ion Channel.

Authors :
Pham T
Perry JL
Dosey TL
Delcour AH
Hyser JM
Source :
Scientific reports [Sci Rep] 2017 Mar 03; Vol. 7, pp. 43487. Date of Electronic Publication: 2017 Mar 03.
Publication Year :
2017

Abstract

Viroporins are small virus-encoded ion channel proteins. Most viroporins are monovalent selective cation channels, with few showing the ability to conduct divalent cations, like calcium (Ca <superscript>2+</superscript> ). Nevertheless, some viroporins are known to disrupt host cell Ca <superscript>2+</superscript> homeostasis, which is critical for virus replication and pathogenesis. Rotavirus nonstructural protein 4 (NSP4) is an endoplasmic reticulum transmembrane glycoprotein that has a viroporin domain (VPD), and NSP4 viroporin activity elevates cytosolic Ca <superscript>2+</superscript> in mammalian cells. The goal of this study was to demonstrate that the NSP4 VPD forms an ion channel and determine whether the channel can conduct Ca <superscript>2+</superscript> . Using planar lipid bilayer and liposome patch clamp electrophysiology, we show that a synthetic peptide of the NSP4 VPD has ion channel activity. The NSP4 VPD was selective for cations over anions and channel activity was observed to have both well-defined "square top" openings as well as fast current fluctuations, similar to other viroporins. Importantly, the NSP4 VPD showed similar conductance of divalent cations (Ca <superscript>2+</superscript> and Ba <superscript>2+</superscript> ) as monovalent cations (K <superscript>+</superscript> ), but a viroporin defective mutant lacked Ca <superscript>2+</superscript> conductivity. These data demonstrate that the NSP4 VPD is a Ca <superscript>2+</superscript> -conducting viroporin and establish the mechanism by which NSP4 disturbs host cell Ca <superscript>2+</superscript> homeostasis.

Details

Language :
English
ISSN :
2045-2322
Volume :
7
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
28256607
Full Text :
https://doi.org/10.1038/srep43487