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Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms

Separating and purifying cell membrane-associated biomolecules has been a challenge owing to their amphiphilic property. Taking these species out of their native lipid membrane environment usually results in biomolecule degradation. One of the new directions is to use supported lipid bilayer (SLB) p...

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Autores principales: Hu, Shu-Kai, Hsiao, Sheng-Wen, Mao, Hsun-Yen, Chen, Ya-Ming, Chang, Yung, Chao, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090319/
https://www.ncbi.nlm.nih.gov/pubmed/27877593
http://dx.doi.org/10.1088/1468-6996/14/4/044408
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author Hu, Shu-Kai
Hsiao, Sheng-Wen
Mao, Hsun-Yen
Chen, Ya-Ming
Chang, Yung
Chao, Ling
author_facet Hu, Shu-Kai
Hsiao, Sheng-Wen
Mao, Hsun-Yen
Chen, Ya-Ming
Chang, Yung
Chao, Ling
author_sort Hu, Shu-Kai
collection PubMed
description Separating and purifying cell membrane-associated biomolecules has been a challenge owing to their amphiphilic property. Taking these species out of their native lipid membrane environment usually results in biomolecule degradation. One of the new directions is to use supported lipid bilayer (SLB) platforms to separate the membrane species while they are protected in their native environment. Here we used a type of crosslinkable diacetylene phospholipids, diynePC (1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine), as a packed material to create a ‘two-dimensional (2D) packed bed’ in a SLB platform. After the diynePC SLB is exposed to UV light, some of the diynePC lipids in the SLB can crosslink and the non-crosslinked monomer lipids can be washed away, leaving a 2D porous solid matrix. We incorporated the lipid vesicle deposition method with a microfluidic device to pattern the location of the packed-bed region and the feed region with species to be separated in a SLB platform. Our atomic force microscopy result shows that the nano-scaled structure density of the ‘2D packed bed’ can be tuned by the UV dose applied to the diynePC membrane. When the model membrane biomolecules were forced to transport through the packed-bed region, their concentration front velocities were found to decrease linearly with the UV dose, indicating the successful creation of packed obstacles in these 2D lipid membrane separation platforms.
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spelling pubmed-50903192016-11-22 Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms Hu, Shu-Kai Hsiao, Sheng-Wen Mao, Hsun-Yen Chen, Ya-Ming Chang, Yung Chao, Ling Sci Technol Adv Mater Focus Articles Separating and purifying cell membrane-associated biomolecules has been a challenge owing to their amphiphilic property. Taking these species out of their native lipid membrane environment usually results in biomolecule degradation. One of the new directions is to use supported lipid bilayer (SLB) platforms to separate the membrane species while they are protected in their native environment. Here we used a type of crosslinkable diacetylene phospholipids, diynePC (1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine), as a packed material to create a ‘two-dimensional (2D) packed bed’ in a SLB platform. After the diynePC SLB is exposed to UV light, some of the diynePC lipids in the SLB can crosslink and the non-crosslinked monomer lipids can be washed away, leaving a 2D porous solid matrix. We incorporated the lipid vesicle deposition method with a microfluidic device to pattern the location of the packed-bed region and the feed region with species to be separated in a SLB platform. Our atomic force microscopy result shows that the nano-scaled structure density of the ‘2D packed bed’ can be tuned by the UV dose applied to the diynePC membrane. When the model membrane biomolecules were forced to transport through the packed-bed region, their concentration front velocities were found to decrease linearly with the UV dose, indicating the successful creation of packed obstacles in these 2D lipid membrane separation platforms. Taylor & Francis 2013-08-23 /pmc/articles/PMC5090319/ /pubmed/27877593 http://dx.doi.org/10.1088/1468-6996/14/4/044408 Text en © 2013 National Institute for Materials Science http://creativecommons.org/licenses/by-nc-sa/3.0/ Content from this work may be used under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 licence (http://creativecommons.org/licenses/by-nc-sa/3.0) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.
spellingShingle Focus Articles
Hu, Shu-Kai
Hsiao, Sheng-Wen
Mao, Hsun-Yen
Chen, Ya-Ming
Chang, Yung
Chao, Ling
Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
title Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
title_full Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
title_fullStr Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
title_full_unstemmed Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
title_short Using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
title_sort using crosslinkable diacetylene phospholipids to construct two-dimensional packed beds in supported lipid bilayer separation platforms
topic Focus Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090319/
https://www.ncbi.nlm.nih.gov/pubmed/27877593
http://dx.doi.org/10.1088/1468-6996/14/4/044408
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