Domain structure of the plasma membrane : interaction between membrane skeleton and membrane receptors
Domain structure of the plasma membrane : interaction between membrane skeleton and membrane receptors
批准号:
04833003
负责人:
SAKO Yasushi
金额:
$1.28万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1992
资助国家:
日本
项目状态:
已结题
起止时间:
1992 至 1993
中文摘要
用40 nm胶体金包被转铁蛋白受体,用纳米级特殊精度和视频速率时间分辨率的视频增强对比光学显微镜研究了转铁蛋白受体分子在培养的正常大鼠肾成纤维细胞质膜中的运动。在-0.25微米^2的区域内,大部分的运动轨迹是受限扩散型的。区域内的运动是随机的,扩散系数为-10^~(-9)cm^2/S,这与蛋白质在质膜中的自由布朗扩散的预期一致。受体分子以0.034s^~(-1)~(-1)~(-1)的平均频率从一个结构域移动到相邻的一个结构域,这表明质膜是为膜受体的扩散而划分的,长距离扩散是连续间隔跳跃的结果。细胞骨架的部分破坏表明,隔室之间的边界是由动态波动的膜骨架组成的。
英文摘要
Movements of transferrin receptor molecules in the plasma membrane of cultured normal rat kidney fibroblastic cells were investigated by video-enhanced contrast optical microscopy with nanometer-level special precision and video-rate temporal resolution by lebeling the receptor with the ligand-coated 40-nm colloidal gold particles. Most of the movement trajectories are of the confined diffusion type within domains of -0.25mum^2. Movement within the domains is random with a diffusion coefficient -10^<-9> cm^2/s, which is consistent with that expected for free Brownian diffusion of proteins in the plasma membrane. The receptor molecules move from one domain to one of the adjacent domains at an average frequency of 0.034s^<-1>, indicating that the plasma membrane is compartmentalized for diffusion of membrane receptors and that long-range diffusion is the result of successive intercompartmental jumps. Partial destruction of the cytoskeleton suggest that the boundaries between compartments are made of dynamically fluctuating membrane skeletons.
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Kusumi A.et al.: "Confined lateral diffusion of membrane receptors as observed by single particle tracking(nanovid microscopy):Effects of calcium-induced differentiation of epithelial cells." Biophysical Journal. 65. 2021-2040 (1993)
Kusumi A.等人:“通过单粒子追踪(纳米维德显微镜)观察到的膜受体的受限横向扩散:钙诱导的上皮细胞分化的影响。”
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通讯作者:
Kusumi, A., Sako, Y., and Yamamoto, M.: "Confined lateral diffusion of membrane receptors as studied by single particle tracking (nanovid microscopy). Effects of calcium-induced differentiation in cultured epithelial cells." Biophys.J.65. 2021-2040 (1993)
Kusumi, A.、Sako, Y. 和 Yamamoto, M.:“通过单粒子追踪(纳米维德显微镜)研究膜受体的有限横向扩散。钙诱导的培养上皮细胞分化的影响。”
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Oida, T., Sako, Y., and Kusumi, A.: "Fluorescence lifetime imaging microscopy (flimscopy). Methodology development and application to studies of endosome fusion in single cells." Biophys.J.64. 676-685 (1993)
Oida, T.、Sako, Y. 和 Kusumi, A.:“荧光寿命成像显微镜(薄镜)。方法开发及其在单细胞内体融合研究中的应用。”
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通讯作者:
Oida,T.et al.: "Fluorescence lifotime imaging microscopy(flimscopy).Methodology development and application to studies of endosome fusion in single cells." Biophysical Journal. (1993)
Oida,T.et al.:“荧光实时成像显微镜(flimscopy)。单细胞内体融合研究的方法学开发和应用。”
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通讯作者:
Sako,Y.et al.: "Compartmeutalized structure of the plasmamembrane for receptor movements as revealed by a nanoweter-level motion analysis" The Jorrnal of Cell Biology. 125. 1251-1264 (1994)
Sako,Y.等人:“通过纳米级运动分析揭示了受体运动的质膜的分隔结构”《细胞生物学杂志》。
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共 6 条
Direct observation of single particle movements in the cytoplasm
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Raman spectrum analysis of cell differentiation dynamics
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Measurements and analysis of fluctuations in cellular systems
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财政年份:2007
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依托单位:
Single-molecule analysis of the spatio-temporal properties of cell signaling processes by small GTPases.
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Development of an in vivo single-molecule fluorescence microscope and its application to the studies of cell signaling
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Development of the single-molecule technique to visualize protein-protein interactions in living cell and its application to the studies of cell signaling
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依托单位:
Development of Super Sensitive Position Detector and Its Application on the Studies of Plasma Membrane Proteins
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批准号:08558075
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负责人:SAKO Yasushi
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依托单位:
海外基金