Structural analysis of the molecular organization of the membrane undercoat
Structural analysis of the molecular organization of the membrane undercoat
批准号:
14380315
负责人:
USUKURA Jiro
金额:
$9.54万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2004
中文摘要
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英文摘要
Cell membrane consists of domains with distinct functions and different sizes, which also plays most important roles in life. Peripheral membrane proteins forming membrane undercoat regulate function and movement of intrinsic membrane proteins within various domains. This project aimed to reveal molecular organization of such membrane undercoat. For this purpose immuno-freeze-etching replica method combined with electron microscopic tomography was employed and available for three-dimensional analysis of membrane undercoat of neural growth cone. In common, membrane undercoat consisted of actin filaments, microtubules, actin related proteins (Arp2/3) and small amount of spectrin. Those filaments formed complicated meshwork and attached closely onto the cytoplasmic surface of the plasma membrane. It is very interested what and how neuronal growth factors are associated in this membrane undercoat. In particular, we focused on CRMP-2 because it was involved in initial formation of axon. Alt … More hough CRMP-2 were localized predominantly on microtubules in axons, it was found frequently on clathrin coats being associated with other unknown particles in membrane undercoat of growth cone. This suggests that CRMP-2 is supposed to participate in endocytosis in the growth cone as well.However, the exact function of CRMP-2 has not been unknown. If CRMP-2 controls growing axon by regulating microtubules and/or actin filaments assembly as the substrate of Rho-kinase in axon, it may have different function in growth cone such as the membrane recycling. We also have been trying to observe the membrane undercoat at living state without any decoration.Fortunately, hydrated membrane undercoat was observed directly under the electron microscope equipped with liquid helium cooled stage using the cell unroofed by original method. Microtubles, actin filaments and clathrin coated pits were found in the similar way of freeze-etching method. This success is a very important step for forthcoming research project. Less
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A critical role for ATP in the stimulation of retinal guanylyl cyclase by guanlyly cyclase-activating proteins (GCAPs)
ATP 在鸟苷酸环化酶激活蛋白 (GCAP) 刺激视网膜鸟苷酸环化酶中的关键作用
DOI:
--
发表时间:
2003
期刊:
J.Biol.Chem. 278
影响因子:
--
作者:
[Usukura Jiro]
通讯作者:
Usukura Jiro
The reconstituted human Ch112-RFC complex functions as a second PC NA loader.
重组的人类 Ch112-RFC 复合物充当第二个 PC NA 加载程序。
DOI:
--
发表时间:
2004
期刊:
Genes to Cells 9
影响因子:
--
作者:
[Usukura Jiro]
通讯作者:
Usukura Jiro
Jiro Usukura: "Characterization of mammalian synemin, an intermediate filament protein present in all four classes of muscle cells and some neuroglial cells : colocalization and interaction with type III intermediate filament proteins and keratins."Cell T
Jiro Usukura:“哺乳动物丝线蛋白(一种存在于所有四类肌肉细胞和一些神经胶质细胞中的中间丝蛋白)的表征:与 III 型中间丝蛋白和角蛋白的共定位和相互作用。”Cell T
DOI:
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发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Jiro Usukura: "Reconstituted human Chl12-RFC complex functions as a second PCNA loader."Gene to Cells. (In press). (2004)
Jiro Usukura:“重组的人类 Chl12-RFC 复合物可作为第二个 PCNA 装载机。”基因到细胞。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
DOI:
10.1111/j.1356-9597.2004.00749.x
发表时间:
2004-07-01
期刊:
GENES TO CELLS
影响因子:
2.1
作者:
[Kawabata, S, Usukura, J, Amano, M]
通讯作者:
Amano, M
共 18 条
Spatial organization of cytoskeletal actin filaments and their regulatory proteins revealed by advanced methods in electron microscopy.
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批准号:22370056
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$12.23万
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财政年份:2010
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负责人:USUKURA Jiro
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依托单位:
Pilot study on construction of the freeze-etching apparatus to create atomic
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批准号:13558091
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$9.28万
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财政年份:2001
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负责人:USUKURA Jiro
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依托单位:
THE STRUCTURAL ANALYSIS OF PHOTO-TRANSDUCTION PROTEINS
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批准号:10044264
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项目类别:Grant-in-Aid for Scientific Research (B).
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资助金额:$1.54万
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财政年份:1998
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负责人:USUKURA Jiro
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依托单位:
IMAGING OF PHOTOTRANSDUCTION PROCESS IN RENTINAL CELLS
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批准号:08044267
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$1.6万
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财政年份:1996
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负责人:USUKURA Jiro
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依托单位:
DIRECT IMAGING OF E.coil POLYMERASE AND TRANSCRIPTION COMPLEX WITH PROMOTER REGION OF MUTANT DNA (UV5).
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批准号:07457005
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$3.14万
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财政年份:1995
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负责人:USUKURA Jiro
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依托单位:
Imaging of dynamic structure of molecular and cellura organization by ultramicroscopic tequniques.
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批准号:07308070
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$3.2万
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财政年份:1995
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负责人:USUKURA Jiro
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依托单位:
Developmental research on the microscopical imaging of DNA transcription process.
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批准号:06558101
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项目类别:Grant-in-Aid for Developmental Scientific Research (B)
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资助金额:$8.45万
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财政年份:1994
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负责人:USUKURA Jiro
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依托单位: