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Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0
Aquaporin-0 (AQP0) is a lens-specific water channel that also forms membrane junctions. Reconstitution of AQP0 with dimyristoyl phosphatidylcholine (DMPC) and E. coli polar lipids (EPL) yielded well-ordered, double-layered two-dimensional (2D) crystals that allowed electron crystallographic structur...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311914/ https://www.ncbi.nlm.nih.gov/pubmed/25635393 http://dx.doi.org/10.1371/journal.pone.0117371 |
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author | Hite, Richard Kevin Chiu, Po-Lin Schuller, Jan Michael Walz, Thomas |
author_facet | Hite, Richard Kevin Chiu, Po-Lin Schuller, Jan Michael Walz, Thomas |
author_sort | Hite, Richard Kevin |
collection | PubMed |
description | Aquaporin-0 (AQP0) is a lens-specific water channel that also forms membrane junctions. Reconstitution of AQP0 with dimyristoyl phosphatidylcholine (DMPC) and E. coli polar lipids (EPL) yielded well-ordered, double-layered two-dimensional (2D) crystals that allowed electron crystallographic structure determination of the AQP0-mediated membrane junction. The interacting tetramers in the two crystalline layers are exactly in register, resulting in crystals with p422 symmetry. The high-resolution density maps also allowed modeling of the annular lipids surrounding the tetramers. Comparison of the DMPC and EPL bilayers suggested that the lipid head groups do not play an important role in the interaction of annular lipids with AQP0. We now reconstituted AQP0 with the anionic lipid dimyristoyl phosphatidylglycerol (DMPG), which yielded a mixture of 2D crystals with different symmetries. The different crystal symmetries result from shifts between the two crystalline layers, suggesting that the negatively charged PG head group destabilizes the interaction between the extracellular AQP0 surfaces. Reconstitution of AQP0 with dimyristoyl phosphatidylserine (DMPS), another anionic lipid, yielded crystals that had the usual p422 symmetry, but the crystals showed a pH-dependent tendency to stack through their cytoplasmic surfaces. Finally, AQP0 failed to reconstitute into membranes that were composed of more than 40% dimyristoyl phosphatidic acid (DMPA). Hence, although DMPG, DMPS, and DMPA are all negatively charged lipids, they have very different effects on AQP0 2D crystals, illustrating the importance of the specific lipid head group chemistry beyond its mere charge. |
format | Online Article Text |
id | pubmed-4311914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43119142015-02-13 Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 Hite, Richard Kevin Chiu, Po-Lin Schuller, Jan Michael Walz, Thomas PLoS One Research Article Aquaporin-0 (AQP0) is a lens-specific water channel that also forms membrane junctions. Reconstitution of AQP0 with dimyristoyl phosphatidylcholine (DMPC) and E. coli polar lipids (EPL) yielded well-ordered, double-layered two-dimensional (2D) crystals that allowed electron crystallographic structure determination of the AQP0-mediated membrane junction. The interacting tetramers in the two crystalline layers are exactly in register, resulting in crystals with p422 symmetry. The high-resolution density maps also allowed modeling of the annular lipids surrounding the tetramers. Comparison of the DMPC and EPL bilayers suggested that the lipid head groups do not play an important role in the interaction of annular lipids with AQP0. We now reconstituted AQP0 with the anionic lipid dimyristoyl phosphatidylglycerol (DMPG), which yielded a mixture of 2D crystals with different symmetries. The different crystal symmetries result from shifts between the two crystalline layers, suggesting that the negatively charged PG head group destabilizes the interaction between the extracellular AQP0 surfaces. Reconstitution of AQP0 with dimyristoyl phosphatidylserine (DMPS), another anionic lipid, yielded crystals that had the usual p422 symmetry, but the crystals showed a pH-dependent tendency to stack through their cytoplasmic surfaces. Finally, AQP0 failed to reconstitute into membranes that were composed of more than 40% dimyristoyl phosphatidic acid (DMPA). Hence, although DMPG, DMPS, and DMPA are all negatively charged lipids, they have very different effects on AQP0 2D crystals, illustrating the importance of the specific lipid head group chemistry beyond its mere charge. Public Library of Science 2015-01-30 /pmc/articles/PMC4311914/ /pubmed/25635393 http://dx.doi.org/10.1371/journal.pone.0117371 Text en © 2015 Hite 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hite, Richard Kevin Chiu, Po-Lin Schuller, Jan Michael Walz, Thomas Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 |
title | Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 |
title_full | Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 |
title_fullStr | Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 |
title_full_unstemmed | Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 |
title_short | Effect of Lipid Head Groups on Double-Layered Two-Dimensional Crystals Formed by Aquaporin-0 |
title_sort | effect of lipid head groups on double-layered two-dimensional crystals formed by aquaporin-0 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311914/ https://www.ncbi.nlm.nih.gov/pubmed/25635393 http://dx.doi.org/10.1371/journal.pone.0117371 |
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