{"title":"轴突输运模型中PDMS密封封闭微管阵列上q点分布的转变","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":"{\"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}","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}
Transition of Q-dot distribution on microtubule array enclosed by PDMS sealing for axonal transport model
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.