{"title":"Transition of Q-dot distribution on microtubule array enclosed by PDMS sealing for axonal transport model","authors":"K. Fujimoto, H. Shintaku, H. Kotera, R. Yokokawa","doi":"10.1109/MEMSYS.2014.6765839","DOIUrl":null,"url":null,"abstract":"In this paper, we show a reconstruction of kinesin driven transport system in three dimensionally (3D) enclosed channels whose scale is similar to axons. Our experimental method enabled successful motility of a large number of kinesin-labeled Q-dots on microtubules (MTs) in enclosed channels. To control the direction of kinesin motility, we prepared a polarity-defined MT array in channels. Due to the directional motility of kinesin, time evolutional accumulation of transported Q-dot at one end of enclosed channels, where corresponds to microtubule (MT) plus end, was observed. This is the first step for an in vitro model of motor protein-based active transport with a 3D spatial confinement mimicking intracellular environment, which is applicable to analyze a regulation mechanism of intracellular transport.","PeriodicalId":312056,"journal":{"name":"2014 IEEE 27th International Conference on Micro Electro Mechanical Systems (MEMS)","volume":"45 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2014-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2014 IEEE 27th International Conference on Micro Electro Mechanical Systems (MEMS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/MEMSYS.2014.6765839","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
In this paper, we show a reconstruction of kinesin driven transport system in three dimensionally (3D) enclosed channels whose scale is similar to axons. Our experimental method enabled successful motility of a large number of kinesin-labeled Q-dots on microtubules (MTs) in enclosed channels. To control the direction of kinesin motility, we prepared a polarity-defined MT array in channels. Due to the directional motility of kinesin, time evolutional accumulation of transported Q-dot at one end of enclosed channels, where corresponds to microtubule (MT) plus end, was observed. This is the first step for an in vitro model of motor protein-based active transport with a 3D spatial confinement mimicking intracellular environment, which is applicable to analyze a regulation mechanism of intracellular transport.