Characterization of the Membrane Transport Assay System Using Microchamber Array

H. Suzuki, K. Tabata, H. Noji, S. Takeuchi
{"title":"Characterization of the Membrane Transport Assay System Using Microchamber Array","authors":"H. Suzuki, K. Tabata, H. Noji, S. Takeuchi","doi":"10.1109/MMB.2006.251556","DOIUrl":null,"url":null,"abstract":"We have been developing a measurement system for membrane transport across a reconstituted planar lipid bilayer to examine the functions of transporter membrane proteins using a microchamber array (membrane microchamber system). In this system, an artificial planar lipid bilayer is pressed on the parylene microchamber array (typically 0.1~1 pL in volume) fabricated on a coverglass to enclose the volume. After membrane proteins are reconstituted in the bilayer, fluorescently labeled molecules transported across the bilayer are accumulated in microchambers, and detected by fluorescent imaging. The microchamber array is compatible with high-sensitive biological imaging techniques, such as a confocal microscopy and a total internal reflection fluorescence microscopy (TIRFM). Due to the tiny volume of microchambers, concentration of the transported molecules rapidly increases. In this study, the detection system was characterized in detail. With the aid of microchambers, the concentration reached to the detectable level with as small as 102~103 fluorescent molecules","PeriodicalId":170356,"journal":{"name":"2006 International Conference on Microtechnologies in Medicine and Biology","volume":"12 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2006-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2006 International Conference on Microtechnologies in Medicine and Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MMB.2006.251556","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

We have been developing a measurement system for membrane transport across a reconstituted planar lipid bilayer to examine the functions of transporter membrane proteins using a microchamber array (membrane microchamber system). In this system, an artificial planar lipid bilayer is pressed on the parylene microchamber array (typically 0.1~1 pL in volume) fabricated on a coverglass to enclose the volume. After membrane proteins are reconstituted in the bilayer, fluorescently labeled molecules transported across the bilayer are accumulated in microchambers, and detected by fluorescent imaging. The microchamber array is compatible with high-sensitive biological imaging techniques, such as a confocal microscopy and a total internal reflection fluorescence microscopy (TIRFM). Due to the tiny volume of microchambers, concentration of the transported molecules rapidly increases. In this study, the detection system was characterized in detail. With the aid of microchambers, the concentration reached to the detectable level with as small as 102~103 fluorescent molecules
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
微室阵列表征膜转运检测系统
我们一直在开发一种测量系统,用于跨重构平面脂质双分子层的膜运输,以使用微室阵列(膜微室系统)检查转运膜蛋白的功能。在该系统中,将人造平面脂质双分子层压在盖玻璃上制备的聚对二甲苯微室阵列(体积通常为0.1~1 pL)上以封闭体积。膜蛋白在双分子层中重组后,通过双分子层运输的荧光标记分子在微室中积累,并通过荧光成像检测。微室阵列兼容高灵敏度的生物成像技术,如共聚焦显微镜和全内反射荧光显微镜(TIRFM)。由于微室体积小,被输送分子的浓度迅速增加。在本研究中,对检测系统进行了详细的表征。在微室的辅助下,小到102~103个荧光分子的浓度就达到了可检测的水平
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
PDF Not Yet Available In IEEE Xplore Two-Compartments Microbioreactor with Integrated Magnetic Stirrer Pump for Measurement of Transmembrane Transport of Caco-2 Cells 3D Microelectrodes for Coulometric Screening in Microfabricated Lab-on-a-Chip Devices A Silicon-Based Single-Cell Electroporation Microchip for Gene Transfer Adsorption-induced inactivation of heavy meromyosin on polymer surfaces imposes effective drag force on sliding actin filaments in vitro
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1