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Functional dissection of motility initiation in sea-urchin sperm flagella

Functional dissection of motility initiation in sea-urchin sperm flagella
海胆精子鞭毛运动启动的功能解剖
批准号:
10640662
负责人:
BABA Shoji A.
金额:
$2.18万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999

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中文摘要
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英文摘要
I improved the temporal and spacial resolution of stroboscopic micrography investing electronic circuitry for driving a high power xenon flash. This enabled us utilizing 35-mm microfilm of excellent granularity for higher spacial resolution. The new stroboscope could work at as high as 6 kHz. I wrote an image analysis software, Bohboh. exe, which can be executed on Microsoft Windows 9x/NT.The analysis of motility initiation in sea-urchin sperm flagella by these novel techniques revealed distinct motility states in stages: bend-unbend stage, p-bend-only stage and steady flagellar beating stage.The analysis of movement at relative high temporal resolution together with very high spacial resolution of sea-urchin sperm reactivated around 10 μM revealed clustered activation of motor molecule dynein local between one or two doublet pair and distributed helically along the axoneme.
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Momoko O. Miyake, Yoshihiro Mogami, Eri Kataoka, Eri Kajita, and Shoji A. Baba: "Improvement in time and space resolution of stroboscopic micrography using high power xenon flash"Rev. Sci. Instrum.. 69-1. 325-326 (1998)
Momoko O. Miyake、Yoshihiro Mogami、Eri Kataoka、Eri Kajita 和 Shoji A. Baba:“使用高功率氙闪光灯改善频闪显微摄影的时间和空间分辨率”Rev。
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