Poly(ethylene glycol) (PEG) is used widely to mediate cell-cell fusion in the production of somatic cell hybrids and in the fusion injection of macromolecules into cultured cells from erythrocytes or liposomes. However, little is known about the mechanism by which PEG induces fusion of cell membranes. The proposed research will continue to examine in molecular detail the influence of PEG on phospholipid vesicles as a model for events in more complex biological membranes. The primary is to elucidate the mechanism of PEG-mediated membrane fusion. The information obtained will be useful for advancing PEG- mediated cell fusion technologies as well as for providing clues to the molecular mechanism of in vivo cell fusion processes such as endocytosis, exocytotic excretion, protein sorting and transport, and viral budding and infection. Work of the past grant period led to a hypothesis for the mechanism of PEG-mediated fusion: formation of fusion intermediates occurs when bilayers containing fluctuational lipid packing defects in the glycerol backbone region are brought into molecular contact by the dehydrating influence of PEG. The resulting probability of fusion is proportional to both the probability of critical inter-bilayer approach and to the probability of packing disruption in either the inner or outer leaflet of the bilayer. The proposed experiments are organized into six aims that will test and then apply this hypothesis to increasingly more complex membranes including ones treated with a viral fusion peptide and cultured cell membranes: 1] test several bilayer components and bilayer conditions for fusogenicity; 2] elaborate the bilayer structural characteristics associated with fusion; 3] test for a critical bilayer structure that seems to correlate with fusion; 4] using several spectroscopic approaches, test whether there exists a common perturbation in bilayer packing associated with PEG-mediated fusion of different model membranes; 5] examine how a very small quantity of the N-terminal """"""""fusion peptide"""""""" of influenza virus hemagglutinin induces fusion of membranes aggregated by low concentrations of PEG; and 6] determine whether bilayer perturbants that act as fusogens in model membranes will increase the efficiency of PEG-mediated fusion of cultured cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM032707-12S1
Application #
2611776
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1983-12-01
Project End
1998-04-14
Budget Start
1996-07-01
Budget End
1998-04-14
Support Year
12
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Biochemistry
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Tarafdar, Pradip K; Chakraborty, Hirak; Bruno, Michael J et al. (2015) Phosphatidylserine-Dependent Catalysis of Stalk and Pore Formation by Synaptobrevin JMR-TMD Peptide. Biophys J 109:1863-72
Sengupta, Tanusree; Chakraborty, Hirak; Lentz, Barry R (2014) The transmembrane domain peptide of vesicular stomatitis virus promotes both intermediate and pore formation during PEG-mediated vesicle fusion. Biophys J 107:1318-26
Chakraborty, Hirak; Sengupta, Tanusree; Lentz, Barry R (2014) pH Alters PEG-mediated fusion of phosphatidylethanolamine-containing vesicles. Biophys J 107:1327-38
Chakraborty, Hirak; Tarafdar, Pradip K; Klapper, David G et al. (2013) 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. Biophys J 105:2495-506
Tenchov, Boris G; MacDonald, Robert C; Lentz, Barry R (2013) Fusion peptides promote formation of bilayer cubic phases in lipid dispersions. An x-ray diffraction study. Biophys J 104:1029-37
Chakraborty, Hirak; Tarafdar, Pradip K; Lentz, Barry R (2013) A novel assay for detecting fusion pore formation: implications for the fusion mechanism. Biochemistry 52:8510-7
Majumder, Rinku; Koklic, Tilen; Rezaie, Alireza R et al. (2013) Phosphatidylserine-induced factor Xa dimerization and binding to factor Va are competing processes in solution. Biochemistry 52:143-51
Tarafdar, Pradip K; Chakraborty, Hirak; Dennison, S Moses et al. (2012) Phosphatidylserine inhibits and calcium promotes model membrane fusion. Biophys J 103:1880-9
Chakraborty, Hirak; Lentz, Barry R (2012) A simple method for correction of circular dichroism spectra obtained from membrane-containing samples. Biochemistry 51:1005-8
Majumder, Rinku; Liang, Xiaoe; Quinn-Allen, Mary Ann et al. (2011) Modulation of prothrombinase assembly and activity by phosphatidylethanolamine. J Biol Chem 286:35535-42

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