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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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. |
format | Online Article Text |
id | pubmed-4806843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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