Literature DB >> 8648293

Comparison of transient and successful fusion pores connecting influenza hemagglutinin expressing cells to planar membranes.

G B Melikyan1, W D Niles, V A Ratinov, M Karhanek, J Zimmerberg, F S Cohen.   

Abstract

Time-resolved admittance measurements were used to investigate the evolution of fusion pores formed between cells expressing influenza virus hemagglutinin (HA) and planar bilayer membranes. The majority of fusion pores opened in a stepwise fashion to semistable conductance levels of several nS. About 20% of the pores had measurable rise times to nS conductances; some of these opened to conductances of approximately 500 pS where they briefly lingered before opening further to semistable conductances. The fall times of closing were statistically similar to the rise times of opening. All fusion pores exhibited semistable values of conductance, varying from approximately 2-20 nS; they would then either close or fully open to conductances on the order of 1 microS. The majority of pores closed; approximately 10% fully opened. Once within the semistable stage, all fusion pores, even those that eventually closed, tended to grow. Statistically, however, before closing, transient fusion pores ceased to grow and reversed their conductance pattern: conductances decreased with a measurable time course until a final drop to closure. In contrast, pore enlargement to the fully open state tended to occur from the largest conductance values attained during a pore's semistable stage. This final enlargement was characterized by a stepwise increase in conductance. The density of HA on the cell surface did not strongly affect pore dynamics. But increased proteolytic treatment of cell surfaces did lead to faster growth within the semistable range. Transient pores and pores that fully opened had indistinguishable initial conductances and statistically identical time courses of early growth, suggesting they were the same upon formation. We suggest that transient and fully open pores evolved from common structures with stochastic factors determining their fate.

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Year:  1995        PMID: 8648293      PMCID: PMC2229290          DOI: 10.1085/jgp.106.5.803

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  19 in total

1.  Hemifusion between cells expressing hemagglutinin of influenza virus and planar membranes can precede the formation of fusion pores that subsequently fully enlarge.

Authors:  V I Razinkov; G B Melikyan; F S Cohen
Journal:  Biophys J       Date:  1999-12       Impact factor: 4.033

2.  Reversible merger of membranes at the early stage of influenza hemagglutinin-mediated fusion.

Authors:  E Leikina; L V Chernomordik
Journal:  Mol Biol Cell       Date:  2000-07       Impact factor: 4.138

3.  Stalk phase formation: effects of dehydration and saddle splay modulus.

Authors:  Yonathan Kozlovsky; Avishay Efrat; David P Siegel; David A Siegel; Michael M Kozlov
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

4.  Membrane permeability changes at early stages of influenza hemagglutinin-mediated fusion.

Authors:  V A Frolov; A Y Dunina-Barkovskaya; A V Samsonov; J Zimmerberg
Journal:  Biophys J       Date:  2003-09       Impact factor: 4.033

5.  Capacitance flickers and pseudoflickers of small granules, measured in the cell-attached configuration.

Authors:  K Lollike; N Borregaard; M Lindau
Journal:  Biophys J       Date:  1998-07       Impact factor: 4.033

6.  Effects of membrane potential and sphingolipid structures on fusion of Semliki Forest virus.

Authors:  Andrey V Samsonov; Prodyot K Chatterjee; Vladimir I Razinkov; Christina H Eng; Margaret Kielian; Fredric S Cohen
Journal:  J Virol       Date:  2002-12       Impact factor: 5.103

7.  Wild-type and mutant hemagglutinin fusion peptides alter bilayer structure as well as kinetics and activation thermodynamics of stalk and pore formation differently: mechanistic implications.

Authors:  Hirak Chakraborty; Pradip K Tarafdar; David G Klapper; Barry R Lentz
Journal:  Biophys J       Date:  2013-12-03       Impact factor: 4.033

8.  The anti-influenza virus agent 4-GU-DANA (zanamivir) inhibits cell fusion mediated by human parainfluenza virus and influenza virus HA.

Authors:  O Greengard; N Poltoratskaia; E Leikina; J Zimmerberg; A Moscona
Journal:  J Virol       Date:  2000-12       Impact factor: 5.103

9.  SNAREs can promote complete fusion and hemifusion as alternative outcomes.

Authors:  Claudio G Giraudo; Chuan Hu; Daoqi You; Avram M Slovic; Eugene V Mosharov; David Sulzer; Thomas J Melia; James E Rothman
Journal:  J Cell Biol       Date:  2005-07-18       Impact factor: 10.539

10.  A point mutation in the binding subunit of a retroviral envelope protein arrests virus entry at hemifusion.

Authors:  Tatiana Zavorotinskaya; Zhaohui Qian; John Franks; Lorraine M Albritton
Journal:  J Virol       Date:  2004-01       Impact factor: 5.103

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