The gap junction channel forms a dynamically regulated aqueous pathway that mediates direct transfer of ions and small molecules between cells. The channel is composed of two integral membrane structures (each in one plasma membrane) formed of connexin protein. The intercellular communication mediated by junctional channels is considered crucial for normal development and mature function of many tissues. The channels are permeable to all known cytoplasmic second messengers. Therefore, information about how the channel functions, how it is gated, what goes through it, and how these properties can be modulated is of medical, biological and biophysical importance. The gap junction channel is difficult to study in situ because it is inaccessible for the experimental techniques and manipulations commonly applied to other channels - both ends of the channel are inside of cells. Access to the pore is via cytoplasm, so it is difficult to distinguish factors that act directly on the channel from those that act on it via intermediate cellular components. The long-term objective of this proposal is to understand the physiology and bio;physics of the gap junction channel. the approach is to incorporate the channel-forming structure into single phospholipid membranes where its properties can be studied. This proposal is to study the ion channels formed by connexin32, which forms gap junction channels between cells in vivo. Specifically, it is proposed to (1) describe and explore the permeation, gating and modulation of connexin32 channels in single phospholipid bilayers, (2) explore the effects of phosphorylation by protein kinases on the properties of connexin32 channels, and (3) explore the functional roles of specific domains of the connexin molecules. By studying the physiology of connexin channels in an experimentally accessible system, one hopes to understand the regulation of the protein that mediates junctional communication. Coupling by way of gap junction is so widespread that elucidation of this process will undoubtedly have profound effects in many areas of cellular and developmental biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM036044-07
Application #
2178196
Study Section
Physiology Study Section (PHY)
Project Start
1986-08-01
Project End
1996-07-31
Budget Start
1994-08-01
Budget End
1996-07-31
Support Year
7
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Physiology
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Tong, Xuhui; Lopez, William; Ramachandran, Jayalakshmi et al. (2015) Glutathione release through connexin hemichannels: Implications for chemical modification of pores permeable to large molecules. J Gen Physiol 146:245-54
Locke, Darren; Kieken, Fabien; Tao, Liang et al. (2011) Mechanism for modulation of gating of connexin26-containing channels by taurine. J Gen Physiol 138:321-39
Locke, Darren; Bian, Shengjie; Li, Hong et al. (2009) Post-translational modifications of connexin26 revealed by mass spectrometry. Biochem J 424:385-98
Johnstone, Scott; Isakson, Brant; Locke, Darren (2009) Biological and biophysical properties of vascular connexin channels. Int Rev Cell Mol Biol 278:69-118
Locke, Darren; Harris, Andrew L (2009) Connexin channels and phospholipids: association and modulation. BMC Biol 7:52
Yeager, Mark; Harris, Andrew L (2007) Gap junction channel structure in the early 21st century: facts and fantasies. Curr Opin Cell Biol 19:521-8
Locke, Darren; Jamieson, Susan; Stein, Torsten et al. (2007) Nature of Cx30-containing channels in the adult mouse mammary gland. Cell Tissue Res 328:97-107
Tao, Liang; Harris, Andrew L (2007) 2-aminoethoxydiphenyl borate directly inhibits channels composed of connexin26 and/or connexin32. Mol Pharmacol 71:570-9
Harris, Andrew L (2007) Connexin channel permeability to cytoplasmic molecules. Prog Biophys Mol Biol 94:120-43
Ayad, Wafaa A; Locke, Darren; Koreen, Irina V et al. (2006) Heteromeric, but not homomeric, connexin channels are selectively permeable to inositol phosphates. J Biol Chem 281:16727-39

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