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The nuclear membrane organization of leukotriene synthesis
Author(s) -
Asim K. Mandal,
Phil Jones,
Angela M. Bair,
Peter Christmas,
Douglas K. Miller,
Ting-ting D. Yamin,
Douglas Wisniewski,
John G. Menke,
Jilly F. Evans,
Bradley T. Hyman,
Brian J. Bacskai,
Mei Chen,
David Lee,
Boris Nikolic,
Roy J. Soberman
Publication year - 2008
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0808211106
Subject(s) - microbiology and biotechnology , arachidonate 5 lipoxygenase , leukotriene , compartmentalization (fire protection) , chemistry , integral membrane protein , arachidonic acid , membrane , biology , membrane protein , biochemistry , enzyme , immunology , asthma
Leukotrienes (LTs) are signaling molecules derived from arachidonic acid that initiate and amplify innate and adaptive immunity. In turn, how their synthesis is organized on the nuclear envelope of myeloid cells in response to extracellular signals is not understood. We define the supramolecular architecture of LT synthesis by identifying the activation-dependent assembly of novel multiprotein complexes on the outer and inner nuclear membranes of mast cells. These complexes are centered on the integral membrane protein 5-Lipoxygenase-Activating Protein, which we identify as a scaffold protein for 5-Lipoxygenase, the initial enzyme of LT synthesis. We also identify these complexes in mouse neutrophils isolated from inflamed joints. Our studies reveal the macromolecular organization of LT synthesis.

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