File:Ectopic-A-lattice-seams-destabilize-microtubules-ncomms4094-s3.ogv
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Ectopic-A-lattice-seams-destabilize-microtubules-ncomms4094-s3.ogv (Ogg Theora video file, length 26 s, 320 × 132 pixels, 176 kbps, file size: 558 KB)
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DescriptionEctopic-A-lattice-seams-destabilize-microtubules-ncomms4094-s3.ogv |
English: Supplementary Movie 2 B-lattice MTs (red) were assembled using pig brain tubulin labelled with Alexa-680 and Alexa-480 fluorescent dyes and GMPCPP, and A-lattice enriched MTs (green) co-assembled with pig brain tubulin labelled with Alexa-488, Mal3FL and GMPCPP. After separate assembly reactions the B and A-lattice enriched MTs were mixed and added to a flow cell coated with rat kinesin-1 motor protein dimers. The flow cell was flushed with buffer to remove Mal3 and unbound MTs. Buffer containing ATP was added and MT motility observed by timelapse epi-fluorescence microscopy. A-lattice enriched MTs shrink faster than B-lattice MTs. Time is in minutes: seconds:milliseconds. Scale bar is 15 μm. |
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Source | Video file from Katsuki M, Drummond D, Cross R (2014). "Ectopic A-lattice seams destabilize microtubules". Nature Communications. DOI:10.1038/ncomms4094. PMID 24463734. PMC: 3921467. | ||
Author | Katsuki M, Drummond D, Cross R | ||
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This file is licensed under the Creative Commons Attribution 3.0 Unported license.
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current | 00:36, 3 November 2016 | 26 s, 320 × 132 (558 KB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Short title | Supplementary Movie 2 |
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Author | Katsuki M, Drummond D, Cross R |
Usage terms | http://creativecommons.org/licenses/by/3.0/ |
Image title | B-lattice MTs (red) were assembled using pig brain tubulin labelled with Alexa-680 and Alexa-480 fluorescent dyes and GMPCPP, and A-lattice enriched MTs (green) co-assembled with pig brain tubulin labelled with Alexa-488, Mal3FL and GMPCPP. After separate assembly reactions the B and A-lattice enriched MTs were mixed and added to a flow cell coated with rat kinesin-1 motor protein dimers. The flow cell was flushed with buffer to remove Mal3 and unbound MTs. Buffer containing ATP was added and MT motility observed by timelapse epi-fluorescence microscopy. A-lattice enriched MTs shrink faster than B-lattice MTs. Time is in minutes: seconds:milliseconds. Scale bar is 15 μm. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2014-01-27 |