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  Electron Cryomicroscopy: From Molecules to Cells

Baumeister, W. (2014). Electron Cryomicroscopy: From Molecules to Cells. Journal of Physics Conference Series, 522:. doi:10.1088/1742-6596/522/1/012003.

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資料種別: 学術論文

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1742-6596_522_1_012003.pdf (全文テキスト(全般)), 2MB
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https://hdl.handle.net/11858/00-001M-0000-0024-15F5-B
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1742-6596_522_1_012003.pdf
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open access article
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 作成者:
Baumeister, Wolfgang1, 著者           
所属:
1Baumeister, Wolfgang / Molecular Structural Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565142              

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キーワード: TRIPEPTIDYL PEPTIDASE II; 26S PROTEASOME; TOMOGRAPHY
 要旨: Today's biomolecular electron microscopy uses essentially three different imaging modalities: (i) electron crystallography, (ii) single particle analysis and (iii) electron tomography. Ideally, these imaging modalities are applied to frozen-hydrated samples to ensure an optimum preservation of the structures under scrutiny. Electron crystallography requires the existence of two-dimensional crystals. In principle, electron crystallography is a high-resolution technique and it has indeed been demonstrated in a number of cases that near-atomic resolution can be attained. Single-particle analysis is particularly suited for structural studies of large macromolecular complexes. The amount of material needed is minute and some degree of heterogeneity is tolerable since image classification can be used for further 'purification in silico'. In principle, single particle analysis can attain high-resolution but, in practice, this often remains an elusive goal. However, since medium resolution structures can be obtained relatively easily, it often provides an excellent basis for hybrid approaches in which high-resolution structures of components are integrated into the medium resolution structures of the holocomplexes. Electron tomography can be applied to non-repetitive structures. Most supramolecuar structures inside cells fall into this category. In order to obtain three-dimensional structures of objects with unique topologies it is necessary to obtain different views by physical tilting. The challenge is to obtain large numbers of projection images covering as wide a tilt range as possible and, at the same time, to minimize the cumulative electron dose. Cryoelectron tomography provides medium resolution three-dimensional images of a wide range of biological structures from isolated supramolecular assemblies to organelles and cells. It allows the visualization of molecular machines in their functional environment (in situ) and the mapping of entire molecular landscapes.

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言語: eng - English
 日付: 2014
 出版の状態: オンラインで出版済み
 ページ: 5
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): ISI: 000340969200003
DOI: 10.1088/1742-6596/522/1/012003
 学位: -

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出版物 1

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出版物名: Journal of Physics Conference Series
  出版物の別名 : J PHYS CONF SER
  出版物の別名 : ELECTRON MICROSCOPY AND ANALYSIS GROUP CONFERENCE 2013 (EMAG2013)
種別: 連載記事
 著者・編者:
所属:
出版社, 出版地: DIRAC HOUSE, TEMPLE BACK, BRISTOL BS1 6BE, ENGLAND : IOP PUBLISHING LTD
ページ: - 巻号: 522 通巻号: 012003 開始・終了ページ: - 識別子(ISBN, ISSN, DOIなど): ISSN: 1742-6588