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 language | English |
|---|---|
| Pages (from-to) | 419-429 |
| Number of pages | 11 |
| Journal | Virology |
| Volume | 363 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jul 5 2007 |
Bibliographical note
Funding Information:This study was supported by NIAID grant A151517 to R.E.D.
Funding
This study was supported by NIAID grant A151517 to R.E.D.
| Funders | Funder number |
|---|---|
| National Institute of Allergy and Infectious F32-AI286447 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI168214 Jason W. Rosch Diseases National Institute of Allergy and Infectious P30 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R00-AI166116 Christopher D. Radka Diseases National Institute of Allergy and Infectious T32-AI106700 Cydney N. Johnson Diseases National Institute of Allergy and Infectious R01AI192221 Jason W. Rosch Diseases National Inst... | R01AI051517, A151517 |
| Not added | 12714 |
Keywords
- Attachment protein
- Degradation
- Hendra virus
- Membrane fusion
- Paramyxovirus
ASJC Scopus subject areas
- Virology