Photolithographic patterned surface forms size-controlled lipid vesicles

Using traditional 2-D photolithographic methods, surface patterns are made on agarose and used to form lipid vesicles with controlled size and layout. Depending on the size and layout of the patterned structures, the lipid bilayer vesicle size can be tuned and placement can be predetermined. Vesicle...

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Main Authors: M. Gertrude Gutierrez, Shotaro Yoshida, Noah Malmstadt, Shoji Takeuchi
Format: Article
Language:English
Published: AIP Publishing LLC 2018-03-01
Series:APL Bioengineering
Online Access:http://dx.doi.org/10.1063/1.5002604
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spelling doaj-49fc09b5aa754e019a344dc986b0763f2020-11-24T23:42:23ZengAIP Publishing LLCAPL Bioengineering2473-28772018-03-0121016104016104-710.1063/1.5002604005801APBPhotolithographic patterned surface forms size-controlled lipid vesiclesM. Gertrude Gutierrez0Shotaro Yoshida1Noah Malmstadt2Shoji Takeuchi3 Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, Japan Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, Japan Mork Family Department of Chemical Engineering and Materials Science, University of Southern California, 925 Bloom Walk, Los Angeles, California 90089, USA Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo, JapanUsing traditional 2-D photolithographic methods, surface patterns are made on agarose and used to form lipid vesicles with controlled size and layout. Depending on the size and layout of the patterned structures, the lipid bilayer vesicle size can be tuned and placement can be predetermined. Vesicles formed on 2-D patterned surfaces can be harvested for further investigations or can be assayed directly on the patterned surface. Lipid vesicles on the patterned surface are assayed for unilamellarity and protein incorporation, and vesicles are indeed unilamellar as observed from outer leaflet fluorescence quenching. Vesicles successfully incorporate the integral membrane protein α-hemolysin and maintain its membrane transport function.http://dx.doi.org/10.1063/1.5002604
collection DOAJ
language English
format Article
sources DOAJ
author M. Gertrude Gutierrez
Shotaro Yoshida
Noah Malmstadt
Shoji Takeuchi
spellingShingle M. Gertrude Gutierrez
Shotaro Yoshida
Noah Malmstadt
Shoji Takeuchi
Photolithographic patterned surface forms size-controlled lipid vesicles
APL Bioengineering
author_facet M. Gertrude Gutierrez
Shotaro Yoshida
Noah Malmstadt
Shoji Takeuchi
author_sort M. Gertrude Gutierrez
title Photolithographic patterned surface forms size-controlled lipid vesicles
title_short Photolithographic patterned surface forms size-controlled lipid vesicles
title_full Photolithographic patterned surface forms size-controlled lipid vesicles
title_fullStr Photolithographic patterned surface forms size-controlled lipid vesicles
title_full_unstemmed Photolithographic patterned surface forms size-controlled lipid vesicles
title_sort photolithographic patterned surface forms size-controlled lipid vesicles
publisher AIP Publishing LLC
series APL Bioengineering
issn 2473-2877
publishDate 2018-03-01
description Using traditional 2-D photolithographic methods, surface patterns are made on agarose and used to form lipid vesicles with controlled size and layout. Depending on the size and layout of the patterned structures, the lipid bilayer vesicle size can be tuned and placement can be predetermined. Vesicles formed on 2-D patterned surfaces can be harvested for further investigations or can be assayed directly on the patterned surface. Lipid vesicles on the patterned surface are assayed for unilamellarity and protein incorporation, and vesicles are indeed unilamellar as observed from outer leaflet fluorescence quenching. Vesicles successfully incorporate the integral membrane protein α-hemolysin and maintain its membrane transport function.
url http://dx.doi.org/10.1063/1.5002604
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AT noahmalmstadt photolithographicpatternedsurfaceformssizecontrolledlipidvesicles
AT shojitakeuchi photolithographicpatternedsurfaceformssizecontrolledlipidvesicles
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