Surface density of the Hendra G protein modulates Hendra F protein-promoted membrane fusion: Role for Hendra G protein trafficking and degradation

Shannon D. Whitman, Rebecca Ellis Dutch

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Hendra virus, like most paramyxoviruses, requires both a fusion (F) and attachment (G) protein for promotion of cell-cell fusion. Recent studies determined that Hendra F is proteolytically processed by the cellular protease cathepsin L after endocytosis. This unique cathepsin L processing results in a small percentage of Hendra F on the cell surface. To determine how the surface densities of the two Hendra glycoproteins affect fusion promotion, we performed experiments that varied the levels of glycoproteins expressed in transfected cells. Using two different fusion assays, we found a marked increase in fusion when expression of the Hendra G protein was increased, with a 1:1 molar ratio of Hendra F:G on the cell surface resulting in optimal membrane fusion. Our results also showed that Hendra G protein levels are modulated by both more rapid protein turnover and slower protein trafficking than is seen for Hendra F.

Original languageEnglish
Pages (from-to)419-429
Number of pages11
JournalVirology
Volume363
Issue number2
DOIs
StatePublished - Jul 5 2007

Bibliographical note

Funding Information:
This study was supported by NIAID grant A151517 to R.E.D.

Keywords

  • Attachment protein
  • Degradation
  • Hendra virus
  • Membrane fusion
  • Paramyxovirus

ASJC Scopus subject areas

  • Virology

Fingerprint

Dive into the research topics of 'Surface density of the Hendra G protein modulates Hendra F protein-promoted membrane fusion: Role for Hendra G protein trafficking and degradation'. Together they form a unique fingerprint.

Cite this