The Pathway of Membrane Fusion Catalyzed by Influenza Hemagglutinin: Restriction of Lipids, Hemifusion, and Lipidic Fusion Pore Formation

Journal of Cell Biology - Tập 140 Số 6 - Trang 1369-1382 - 1998
Leonid Chernomordik1,2, Vadim A. Frolov1,2, Eugenia Leikina1,2, Peter Bronk1,2, Joshua Zimmerberg1,2
1*Laboratory of Cellular and Molecular Biophysics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-1855; and ‡Laboratory of Bioelectrochemistry, A.N. Frumkin Institute of Electrochemistry, Russian Academy of Science, Moscow, 117071, Russia
2Laboratory of Bioelectrochemistry, A.N. Frumkin Institute of Electrochemistry, Russian Academy of Science, Moscow, 117071, Russia

Tóm tắt

The mechanism of bilayer unification in biological fusion is unclear. We reversibly arrested hemagglutinin (HA)-mediated cell–cell fusion right before fusion pore opening. A low-pH conformation of HA was required to form this intermediate and to ensure fusion beyond it. We present evidence indicating that outer monolayers of the fusing membranes were merged and continuous in this intermediate, but HA restricted lipid mixing. Depending on the surface density of HA and the membrane lipid composition, this restricted hemifusion intermediate either transformed into a fusion pore or expanded into an unrestricted hemifusion, without pores but with unrestricted lipid mixing. Our results suggest that restriction of lipid flux by a ring of activated HA is necessary for successful fusion, during which a lipidic fusion pore develops in a local and transient hemifusion diaphragm.

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