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Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs

An important step in the production of inflammatory mediators of the leukotriene family is the Ca(2+) mediated recruitment of 5 Lipoxygenase (5LO) to nuclear membranes. To study this reaction in vitro, the natural membrane mimicking environment of nanodiscs was used. Nanodiscs with 10.5 nm inner dia...

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Autores principales: Kumar, Ramakrishnan B., Zhu, Lin, Idborg, Helena, Rådmark, Olof, Jakobsson, Per-Johan, Rinaldo-Matthis, Agnes, Hebert, Hans, Jegerschöld, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4806843/
https://www.ncbi.nlm.nih.gov/pubmed/27010627
http://dx.doi.org/10.1371/journal.pone.0152116
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author Kumar, Ramakrishnan B.
Zhu, Lin
Idborg, Helena
Rådmark, Olof
Jakobsson, Per-Johan
Rinaldo-Matthis, Agnes
Hebert, Hans
Jegerschöld, Caroline
author_facet Kumar, Ramakrishnan B.
Zhu, Lin
Idborg, Helena
Rådmark, Olof
Jakobsson, Per-Johan
Rinaldo-Matthis, Agnes
Hebert, Hans
Jegerschöld, Caroline
author_sort Kumar, Ramakrishnan B.
collection PubMed
description An important step in the production of inflammatory mediators of the leukotriene family is the Ca(2+) mediated recruitment of 5 Lipoxygenase (5LO) to nuclear membranes. To study this reaction in vitro, the natural membrane mimicking environment of nanodiscs was used. Nanodiscs with 10.5 nm inner diameter were made with the lipid POPC and membrane scaffolding protein MSP1E3D1. Monomeric and dimeric 5LO were investigated. Monomeric 5LO mixed with Ca(2+) and nanodiscs are shown to form stable complexes that 1) produce the expected leukotriene products from arachidonic acid and 2) can be, for the first time, visualised by native gel electrophoresis and negative stain transmission electron microscopy and 3) show a highest ratio of two 5LO per nanodisc. We interpret this as one 5LO on each side of the disc. The dimer of 5LO is visualised by negative stain transmission electron microscopy and is shown to not bind to nanodiscs. This study shows the advantages of nanodiscs to obtain basic structural information as well as functional information of a complex between a monotopic membrane protein and the membrane.
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spelling pubmed-48068432016-03-25 Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs Kumar, Ramakrishnan B. Zhu, Lin Idborg, Helena Rådmark, Olof Jakobsson, Per-Johan Rinaldo-Matthis, Agnes Hebert, Hans Jegerschöld, Caroline PLoS One Research Article An important step in the production of inflammatory mediators of the leukotriene family is the Ca(2+) mediated recruitment of 5 Lipoxygenase (5LO) to nuclear membranes. To study this reaction in vitro, the natural membrane mimicking environment of nanodiscs was used. Nanodiscs with 10.5 nm inner diameter were made with the lipid POPC and membrane scaffolding protein MSP1E3D1. Monomeric and dimeric 5LO were investigated. Monomeric 5LO mixed with Ca(2+) and nanodiscs are shown to form stable complexes that 1) produce the expected leukotriene products from arachidonic acid and 2) can be, for the first time, visualised by native gel electrophoresis and negative stain transmission electron microscopy and 3) show a highest ratio of two 5LO per nanodisc. We interpret this as one 5LO on each side of the disc. The dimer of 5LO is visualised by negative stain transmission electron microscopy and is shown to not bind to nanodiscs. This study shows the advantages of nanodiscs to obtain basic structural information as well as functional information of a complex between a monotopic membrane protein and the membrane. Public Library of Science 2016-03-24 /pmc/articles/PMC4806843/ /pubmed/27010627 http://dx.doi.org/10.1371/journal.pone.0152116 Text en © 2016 Kumar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kumar, Ramakrishnan B.
Zhu, Lin
Idborg, Helena
Rådmark, Olof
Jakobsson, Per-Johan
Rinaldo-Matthis, Agnes
Hebert, Hans
Jegerschöld, Caroline
Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs
title Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs
title_full Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs
title_fullStr Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs
title_full_unstemmed Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs
title_short Structural and Functional Analysis of Calcium Ion Mediated Binding of 5-Lipoxygenase to Nanodiscs
title_sort structural and functional analysis of calcium ion mediated binding of 5-lipoxygenase to nanodiscs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4806843/
https://www.ncbi.nlm.nih.gov/pubmed/27010627
http://dx.doi.org/10.1371/journal.pone.0152116
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