Heterogeneity of early intermediates in cell-liposome fusion mediated by influenza hemagglutinin

被引:5
|
作者
Zhukovsky, Mikhail A. [1 ]
Leikina, Eugenia [1 ]
Markovic, Ingrid [1 ]
Bailey, Austin L. [1 ]
Chernomordik, Leonid V. [1 ]
机构
[1] NICHHD, Sect Membrane Biol, Cellular & Mol Biophys Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1529/biophysj.106.088005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
To explore early intermediates in membrane fusion mediated by influenza virus hemagglutinin (HA) and their dependence on the composition of the target membrane, we studied lipid mixing between HA-expressing cells and liposomes containing phosphatidylcholine ( PC) with different hydrocarbon chains. For all tested compositions, our results indicate the existence of at least two types of intermediates, which differ in their lifetimes. The composition of the target membrane affects the stability of fusion intermediates at a stage before lipid mixing. For less fusogenic distearoyl PC-containing liposomes at 4 degrees C, some of the intermediates inactivate, and no intermediates advance to lipid mixing. Fusion intermediates that formed for the more fusogenic dioleoyl PC-containing liposomes did not inactivate and even yielded partial lipid mixing at 4 degrees C. Thus, a more fusogenic target membrane effectively blocks nonproductive release of the conformational energy of HA. Even for the same liposome composition, HA forms two types of fusion intermediates, dissimilar in their stability and propensity to fuse. This diversity of fusion intermediates emphasizes the importance of local membrane composition and local protein concentration in fusion of heterogeneous biological membranes.
引用
收藏
页码:3349 / 3358
页数:10
相关论文
共 50 条
  • [31] Raft association plays an important role in Influenza Hemagglutinin-mediated fusion
    Kumar, M
    Kenworthy, AK
    Roth, MG
    Zimmerberg, J
    MOLECULAR BIOLOGY OF THE CELL, 2001, 12 : 74A - 74A
  • [32] Early steps of the conformational change of influenza virus hemagglutinin to a fusion active state -: Stability and energetics of the hemagglutinin
    Huang, Q
    Sivaramakrishna, RP
    Ludwig, K
    Korte, T
    Böttcher, C
    Herrmann, A
    BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1614 (01): : 3 - 13
  • [33] ANALYSIS OF DELAY TIMES OF HEMAGGLUTININ-MEDIATED FUSION BETWEEN INFLUENZA-VIRUS AND CELL-MEMBRANES
    LUDWIG, K
    KORTE, T
    HERRMANN, A
    EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 1995, 24 (02): : 55 - 64
  • [34] Membrane perturbation and fusion pore formation in influenza hemagglutinin-mediated membrane fusion - A new model for fusion
    Bonnafous, P
    Stegmann, T
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) : 6160 - 6166
  • [35] Dilation of the influenza hemagglutinin fusion pore revealed by the kinetics of individual cell-cell fusion events
    Blumenthal, R
    Sarkar, DP
    Durell, S
    Howard, DE
    Morris, SJ
    JOURNAL OF CELL BIOLOGY, 1996, 135 (01): : 63 - 71
  • [36] Influenza-virus membrane fusion by cooperative fold-back of stochastically induced hemagglutinin intermediates
    Ivanovic, Tijana
    Choi, Jason L.
    Whelan, Sean P.
    van Oijen, Antoine M.
    Harrison, Stephen C.
    ELIFE, 2013, 2
  • [37] Individual influenza hemagglutinin-mediated membrane fusion events from fusion pore opening to dilation
    Blumenthal, R
    Sarkar, DP
    Durell, S
    Howard, DE
    Morris, SJ
    BIOPHYSICAL JOURNAL, 1996, 70 (02) : SU292 - SU292
  • [38] Effect of influenza hemagglutinin fusion peptide on lipid intermediates in Lα/HII phase transitions:: Implications for membrane fusion mechanisms.
    Siegel, DP
    Epand, RM
    BIOPHYSICAL JOURNAL, 1998, 74 (02) : A94 - A94
  • [39] Role of microdomain-mediated clustering of influenza hemagglutinin in viral fusion: The ring raft
    Kumar, M
    Kenworthy, AK
    Verma, A
    Roth, MG
    Zimmerberg, J
    BIOPHYSICAL JOURNAL, 2002, 82 (01) : 541A - 541A
  • [40] Fusion mediated by ectodomain of HA2 subunit of influenza virus hemagglutinin.
    Leikina, E
    Kim, CS
    Epand, RF
    Epand, RM
    Shin, YK
    Chernomordik, LV
    BIOPHYSICAL JOURNAL, 2004, 86 (01) : 43A - 43A