Membrane Localization and Topology of Leukotriene C4 Synthase
Leukotriene C 4 (LTC 4 ) synthase conjugates LTA 4 with GSH to form LTC 4 . Determining the site of LTC 4 synthesis and the topology of LTC 4 synthase may uncover unappreciated intracellular roles for LTC 4 , as well as how LTC 4 is transferred to its export carrier, the multidrug resistance protein...
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Veröffentlicht in: | The Journal of biological chemistry 2002-08, Vol.277 (32), p.28902-28908 |
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Sprache: | eng |
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Zusammenfassung: | Leukotriene C 4 (LTC 4 ) synthase conjugates LTA 4 with GSH to form LTC 4 . Determining the site of LTC 4 synthesis and the topology of LTC 4 synthase may uncover unappreciated intracellular roles for LTC 4 , as well as how LTC 4 is transferred to its export carrier, the multidrug resistance protein-1. We have determined the membrane localization of
LTC 4 synthase by immunoelectron microscopy. In contrast to the closely related five-lipoxygenase-activating protein, LTC 4 synthase is distributed in the outer nuclear membrane and peripheral endoplasmic reticulum but is excluded from the inner
nuclear membrane. We have combined immunofluorescence with differential membrane permeabilization to determine the topology
of LTC 4 synthase. The active site of LTC 4 synthase is localized in the lumen of the nuclear envelope and endoplasmic reticulum. These results indicate that the synthesis
of LTB 4 and LTC 4 occurs in different subcellular locations and suggests that LTC 4 must be returned to the cytoplasmic side of the membrane for export by multidrug resistance protein-1. The differential localization
of two very similar integral membrane proteins suggests that mechanisms other than size-dependent exclusion regulate their
passage to the inner nuclear membrane. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.M203074200 |