Cell membrane array fabrication and assay technology

<p>Abstract</p> <p>Background</p> <p>Microarray technology has been used extensively over the past 10 years for assessing gene expression, and has facilitated precise genetic profiling of everything from tumors to small molecule drugs. By contrast, arraying cell membran...

Full description

Bibliographic Details
Main Authors: Brade Lore, Gutsmann Thomas, Nguyen Luat, Schafer Robert J, Sirenko Oksana, Yamazaki Victoria, Groves Jay T
Format: Article
Language:English
Published: BMC 2005-06-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/5/18
id doaj-f5046f80454345de9162f2d899babc1e
record_format Article
spelling doaj-f5046f80454345de9162f2d899babc1e2020-11-25T03:29:30ZengBMCBMC Biotechnology1472-67502005-06-01511810.1186/1472-6750-5-18Cell membrane array fabrication and assay technologyBrade LoreGutsmann ThomasNguyen LuatSchafer Robert JSirenko OksanaYamazaki VictoriaGroves Jay T<p>Abstract</p> <p>Background</p> <p>Microarray technology has been used extensively over the past 10 years for assessing gene expression, and has facilitated precise genetic profiling of everything from tumors to small molecule drugs. By contrast, arraying cell membranes in a manner which preserves their ability to mediate biochemical processes has been considerably more difficult.</p> <p>Results</p> <p>In this article, we describe a novel technology for generating cell membrane microarrays for performing high throughput biology. Our robotically-arrayed supported membranes are physiologically fluid, a critical property which differentiates this technology from other previous membrane systems and makes it useful for studying cellular processes on an industrialized scale. Membrane array elements consist of a solid substrate, above which resides a fluid supported lipid bilayer containing biologically-active molecules of interest. Incorporation of transmembrane proteins into the arrayed membranes enables the study of ligand/receptor binding, as well as interactions with live intact cells. The fluidity of these molecules in the planar lipid bilayer facilitates dimerization and other higher order interactions necessary for biological signaling events. In order to demonstrate the utility of our fluid membrane array technology to ligand/receptor studies, we investigated the multivalent binding of the cholera toxin B-subunit (CTB) to the membrane ganglioside GM<sub>1</sub>. We have also displayed a number of <it>bona fide </it>drug targets, including bacterial endotoxin (also referred to as lipopolysaccharide (LPS)) and membrane proteins important in T cell activation.</p> <p>Conclusion</p> <p>We have demonstrated the applicability of our fluid cell membrane array technology to both academic research applications and industrial drug discovery. Our technology facilitates the study of ligand/receptor interactions and cell-cell signaling, providing rich qualitative and quantitative information.</p> http://www.biomedcentral.com/1472-6750/5/18
collection DOAJ
language English
format Article
sources DOAJ
author Brade Lore
Gutsmann Thomas
Nguyen Luat
Schafer Robert J
Sirenko Oksana
Yamazaki Victoria
Groves Jay T
spellingShingle Brade Lore
Gutsmann Thomas
Nguyen Luat
Schafer Robert J
Sirenko Oksana
Yamazaki Victoria
Groves Jay T
Cell membrane array fabrication and assay technology
BMC Biotechnology
author_facet Brade Lore
Gutsmann Thomas
Nguyen Luat
Schafer Robert J
Sirenko Oksana
Yamazaki Victoria
Groves Jay T
author_sort Brade Lore
title Cell membrane array fabrication and assay technology
title_short Cell membrane array fabrication and assay technology
title_full Cell membrane array fabrication and assay technology
title_fullStr Cell membrane array fabrication and assay technology
title_full_unstemmed Cell membrane array fabrication and assay technology
title_sort cell membrane array fabrication and assay technology
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2005-06-01
description <p>Abstract</p> <p>Background</p> <p>Microarray technology has been used extensively over the past 10 years for assessing gene expression, and has facilitated precise genetic profiling of everything from tumors to small molecule drugs. By contrast, arraying cell membranes in a manner which preserves their ability to mediate biochemical processes has been considerably more difficult.</p> <p>Results</p> <p>In this article, we describe a novel technology for generating cell membrane microarrays for performing high throughput biology. Our robotically-arrayed supported membranes are physiologically fluid, a critical property which differentiates this technology from other previous membrane systems and makes it useful for studying cellular processes on an industrialized scale. Membrane array elements consist of a solid substrate, above which resides a fluid supported lipid bilayer containing biologically-active molecules of interest. Incorporation of transmembrane proteins into the arrayed membranes enables the study of ligand/receptor binding, as well as interactions with live intact cells. The fluidity of these molecules in the planar lipid bilayer facilitates dimerization and other higher order interactions necessary for biological signaling events. In order to demonstrate the utility of our fluid membrane array technology to ligand/receptor studies, we investigated the multivalent binding of the cholera toxin B-subunit (CTB) to the membrane ganglioside GM<sub>1</sub>. We have also displayed a number of <it>bona fide </it>drug targets, including bacterial endotoxin (also referred to as lipopolysaccharide (LPS)) and membrane proteins important in T cell activation.</p> <p>Conclusion</p> <p>We have demonstrated the applicability of our fluid cell membrane array technology to both academic research applications and industrial drug discovery. Our technology facilitates the study of ligand/receptor interactions and cell-cell signaling, providing rich qualitative and quantitative information.</p>
url http://www.biomedcentral.com/1472-6750/5/18
work_keys_str_mv AT bradelore cellmembranearrayfabricationandassaytechnology
AT gutsmannthomas cellmembranearrayfabricationandassaytechnology
AT nguyenluat cellmembranearrayfabricationandassaytechnology
AT schaferrobertj cellmembranearrayfabricationandassaytechnology
AT sirenkooksana cellmembranearrayfabricationandassaytechnology
AT yamazakivictoria cellmembranearrayfabricationandassaytechnology
AT grovesjayt cellmembranearrayfabricationandassaytechnology
_version_ 1724578842866089984