The primary goal of this project is to understand the processes which occur during the fusion of vesicles to planar bilayer membranes and how they relate to the physiological process of exocytosis. The fusion of phospholipid vesicles to planar membranes has been shown to be enhanced by divalent cations which promote the close association of vesicles to the planar membrane. Osmotic swelling of these vesicles is the driving force for fusion. In cell membranes, phospholipids are arranged in a bilayer structure; we will now establish which aspects of biological exocytosis can be accounted for solely on the basis of phospholipid interactions. Utilizing large (10 um) vesicles in which fusion to planar membranes can be electrically assayed by measuring step-wise increases in the capacitance of the planar membrane, the vesicle-planar membrane interactions will be directly viewed under a fluorescence microscope. By loading the vesicles with fluorescent dye we will determine whether soluble vesicular contents are exclusively transferred to the other (trans) side of the planar membrane as occurs in biological exocytosis, or if there is leakage of contents back into the vesicle containing (cis) side. We will determine the pathway by which vesicles come in contact with the planar membrane and establish to what area of the membrane the vesicles fuse. We will observe whether only isolated vesicles fuse to the membrane or compound exocytosis can occur. The efficacy of fusogenic agents will be tested using a previously established conductance assay and their mechanisms of action investigated. To more closely model biological exocytosis, the fusion of biological intracellular secretory granules to planar membranes will be studied. Using catecholamine-containing chromaffin granules we will determine if conductance increases in the planar membrane accompany fusion; and measure release of granule contents to the trans side. The long range effort will be to determine the conditions necessary to induce fusion, the parameters which control its rate, and the forces and energetics - in other words the underlying mechanisms - of the fusion process in this semi-natural system.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM027367-08
Application #
3274767
Study Section
Physiology Study Section (PHY)
Project Start
1980-04-01
Project End
1989-07-31
Budget Start
1988-08-01
Budget End
1989-07-31
Support Year
8
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Rush University
Department
Type
Overall Medical
DUNS #
City
Chicago
State
IL
Country
United States
Zip Code
60612
Leung, Michael Y K; Cohen, Fredric S (2011) Increasing hydrophobicity of residues in an anti-HIV-1 Env peptide synergistically improves potency. Biophys J 100:1960-8
Markosyan, Ruben M; Cohen, Fredric S (2010) Negative potentials across biological membranes promote fusion by class II and class III viral proteins. Mol Biol Cell 21:2001-12
Markosyan, Ruben M; Leung, Michael Y; Cohen, Fredric S (2009) The six-helix bundle of human immunodeficiency virus Env controls pore formation and enlargement and is initiated at residues proximal to the hairpin turn. J Virol 83:10048-57
Markosyan, Ruben M; Kielian, Margaret; Cohen, Fredric S (2007) Fusion induced by a class II viral fusion protein, semliki forest virus E1, is dependent on the voltage of the target cell. J Virol 81:11218-25
Abrahamyan, Levon G; Mkrtchyan, Samvel R; Binley, James et al. (2005) The cytoplasmic tail slows the folding of human immunodeficiency virus type 1 Env from a late prebundle configuration into the six-helix bundle. J Virol 79:106-15
Mkrtchyan, Samvel R; Markosyan, Ruben M; Eadon, Michael T et al. (2005) Ternary complex formation of human immunodeficiency virus type 1 Env, CD4, and chemokine receptor captured as an intermediate of membrane fusion. J Virol 79:11161-9
Markosyan, Ruben M; Cohen, Fredric S; Melikyan, Grigory B (2005) Time-resolved imaging of HIV-1 Env-mediated lipid and content mixing between a single virion and cell membrane. Mol Biol Cell 16:5502-13
Melikyan, G B; Barnard, R J O; Markosyan, R M et al. (2004) Low pH is required for avian sarcoma and leukosis virus Env-induced hemifusion and fusion pore formation but not for pore growth. J Virol 78:3753-62
Markosyan, R M; Bates, P; Cohen, F S et al. (2004) A study of low pH-induced refolding of Env of avian sarcoma and leukosis virus into a six-helix bundle. Biophys J 87:3291-8
Cohen, F S; Melikyan, G B (2004) The energetics of membrane fusion from binding, through hemifusion, pore formation, and pore enlargement. J Membr Biol 199:1-14

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