TY - JOUR
T1 - Surface density of the Hendra G protein modulates Hendra F protein-promoted membrane fusion
T2 - Role for Hendra G protein trafficking and degradation
AU - Whitman, Shannon D.
AU - Dutch, Rebecca Ellis
N1 - Funding Information:
This study was supported by NIAID grant A151517 to R.E.D.
PY - 2007/7/5
Y1 - 2007/7/5
N2 - 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.
AB - 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.
KW - Attachment protein
KW - Degradation
KW - Hendra virus
KW - Membrane fusion
KW - Paramyxovirus
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U2 - 10.1016/j.virol.2007.01.029
DO - 10.1016/j.virol.2007.01.029
M3 - Article
C2 - 17328935
AN - SCOPUS:34248655915
SN - 0042-6822
VL - 363
SP - 419
EP - 429
JO - Virology
JF - Virology
IS - 2
ER -