Epithelial cells, which comprise 50% of all cells in the body [and account for 90% of all human cancers] have as a defining function the creation and maintenance of physiological compartments of the body. They are functionally and morphologically polarized in order to perform this function. Lipid-anchored proteins, GPI=proteins and glycosphingolipids are concentrated at the apical surfaces of most polarized epithelial cells. We propose to use biophysical techniques to study the formation, and organization of the sorting units for GPI-proteins in the Golgi and plasma membranes and to compare the sorting units in MDCK cells, in which GPI-proteins are delivered directly to the apical surface, and in WIF-B hepatocytes, in which apical proteins take an indirect route to the apical surface. We will also compare the lateral organization of different GPI-proteins in MDCK cells and in liposomes. The following questions will be address: 1) How are GPI-proteins and GSL concentrated and segregated from other proteins in the Golgi? 2) What are the cell & protein specificities of the clustering and polarity of GPI-proteins in cells grown in complete medium and abolish their polarity in cells deprived of LDL? Our techniques to address these questions include fluorescence photo bleaching and recovery, FPR, fluorescence loss in photo bleaching, FLIP, and imaging fluorescence resonance energy transfer, FRET.

Project Start
1999-02-01
Project End
1999-12-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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Suzuki, Kenichi G N; Fujiwara, Takahiro K; Sanematsu, Fumiyuki et al. (2007) GPI-anchored receptor clusters transiently recruit Lyn and G alpha for temporary cluster immobilization and Lyn activation: single-molecule tracking study 1. J Cell Biol 177:717-30
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Berezuk, Matthew A; Schroer, Trina A (2004) Fractionation and characterization of kinesin II species in vertebrate brain. Traffic 5:503-13
Nyasae, Lydia K; Hubbard, Ann L; Tuma, Pamela L (2003) Transcytotic efflux from early endosomes is dependent on cholesterol and glycosphingolipids in polarized hepatic cells. Mol Biol Cell 14:2689-705
Tuma, Pamela L; Hubbard, Ann L (2003) Transcytosis: crossing cellular barriers. Physiol Rev 83:871-932
King, Stephen J; Brown, Christa L; Maier, Kerstin C et al. (2003) Analysis of the dynein-dynactin interaction in vitro and in vivo. Mol Biol Cell 14:5089-97
Bastaki, M; Braiterman, L T; Johns, D C et al. (2002) Absence of direct delivery for single transmembrane apical proteins or their ""Secretory"" forms in polarized hepatic cells. Mol Biol Cell 13:225-37
Tuma, Pamela L; Nyasae, Lydia K; Hubbard, Ann L (2002) Nonpolarized cells selectively sort apical proteins from cell surface to a novel compartment, but lack apical retention mechanisms. Mol Biol Cell 13:3400-15
Quintyne, Nicholas J; Schroer, Trina A (2002) Distinct cell cycle-dependent roles for dynactin and dynein at centrosomes. J Cell Biol 159:245-54

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