The long-term objective is to describe the electrostatic and electrokinetic properties of biological membranes. There are six specific aims: (i) to investigate the discreteness-of-charge effect using positive as well as negative membranes, polyvalent as well as monovalent lipids, and frozen as well as fluid bilayers; (ii) to measure the interaction of polyvalent lipids (e.g., phosphatidylinositol 4, 5-bisphosphate, PIP2) with proteins that have several positive charges close to the membrane-solution interface (e.g., glycophorin, melittin, rhodopsin); (iii) to determine the electrostatic potential 1 nm from the surface of a charged membrane; (iv) to investigate the electrostatic and electrokinetic properties of model and biological membranes that have charges a significant distance from the membrane- solution interface; (v) to study the ion exchange properties of PIP2; (vi) to evaluate the role electrostatic potentials play in exocytosis. Established experimental techniques will be used to measure: the conductance of planar bilayers, the surface potential of monolayers, the 31P NMR spectra of sonicated vesicles, the fluorescence (from the probe TNS) of vesicles, and the electrophoretic mobility of both lipid vesicles and biological membranes. A new fluorescence technique will be developed; fluorescent probes will be attached to defined locations on gangliosides, the fluorescence quenched with the cations tempamine or thallium, and the potential estimated from the Boltzmann relation. The results from all these techniques will be compared with the predictions of classical theories (either the Gouy-Stokes equations) and with the predictions of a modern statistical mechanical theory developed by S. Marcelja, who will collaborate on this project. The experimental results, and theoretical concepts that will emerge from these results, are health related because PIP2 is the source of two second messengers in the cell and gangliosides are involved in cell-cell recognition. For example, an antibody with a high affinity for the ganglioside GD3 has recently been shown to be effective in the treatment of melanomas. Information about the biophysical properties of PIP2 and gangliosides should thus be of interest to many physiologists, biochemists, cell biologists and clinicians.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM024971-10
Application #
3272696
Study Section
Physiology Study Section (PHY)
Project Start
1978-04-01
Project End
1992-08-31
Budget Start
1987-09-01
Budget End
1988-08-31
Support Year
10
Fiscal Year
1987
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Sengupta, Parijat; Bosis, Eran; Nachliel, Esther et al. (2009) EGFR juxtamembrane domain, membranes, and calmodulin: kinetics of their interaction. Biophys J 96:4887-95
Golebiewska, Urszula; Nyako, Marian; Woturski, William et al. (2008) Diffusion coefficient of fluorescent phosphatidylinositol 4,5-bisphosphate in the plasma membrane of cells. Mol Biol Cell 19:1663-9
Sengupta, Parijat; Ruano, Maria Jose; Tebar, Francesc et al. (2007) Membrane-permeable calmodulin inhibitors (e.g. W-7/W-13) bind to membranes, changing the electrostatic surface potential: dual effect of W-13 on epidermal growth factor receptor activation. J Biol Chem 282:8474-86
Nomikos, Michail; Mulgrew-Nesbitt, Anna; Pallavi, Payal et al. (2007) Binding of phosphoinositide-specific phospholipase C-zeta (PLC-zeta) to phospholipid membranes: potential role of an unstructured cluster of basic residues. J Biol Chem 282:16644-53
Sato, Takeshi; Pallavi, Payal; Golebiewska, Urszula et al. (2006) Structure of the membrane reconstituted transmembrane-juxtamembrane peptide EGFR(622-660) and its interaction with Ca2+/calmodulin. Biochemistry 45:12704-14
Tao, Jiangchuan; Shumay, Elena; McLaughlin, Stuart et al. (2006) Regulation of AKAP-membrane interactions by calcium. J Biol Chem 281:23932-44
McLaughlin, Stuart; Smith, Steven O; Hayman, Michael J et al. (2005) An electrostatic engine model for autoinhibition and activation of the epidermal growth factor receptor (EGFR/ErbB) family. J Gen Physiol 126:41-53
Wang, Jiyao; Gambhir, Alok; McLaughlin, Stuart et al. (2004) A computational model for the electrostatic sequestration of PI(4,5)P2 by membrane-adsorbed basic peptides. Biophys J 86:1969-86
Gambhir, Alok; Hangyas-Mihalyne, Gyongyi; Zaitseva, Irina et al. (2004) Electrostatic sequestration of PIP2 on phospholipid membranes by basic/aromatic regions of proteins. Biophys J 86:2188-207
Rusu, Laura; Gambhir, Alok; McLaughlin, Stuart et al. (2004) Fluorescence correlation spectroscopy studies of Peptide and protein binding to phospholipid vesicles. Biophys J 87:1044-53

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