+データを開く
-基本情報
登録情報 | データベース: EMDB / ID: EMD-12729 | ||||||||||||
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タイトル | Tomogram of a Drosophila Malpighian tubule vitrified by plunge freezing upon incubation in 10% glycerol | ||||||||||||
マップデータ | Tomogram of a Drosophila Malpighian tubule vitrified by plunge freezing upon incubation in 10% glycerol | ||||||||||||
試料 |
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生物種 | Drosophila melanogaster (キイロショウジョウバエ) | ||||||||||||
手法 | 電子線トモグラフィー法 / クライオ電子顕微鏡法 | ||||||||||||
データ登録者 | Bauerlein FJB / Pastor-Pareja JC / Fernandez-Busnadiego R | ||||||||||||
資金援助 | ドイツ, 中国, 3件
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引用 | ジャーナル: To Be Published タイトル: Cryo-electron tomography of native Drosophila tissues vitrified by plunge freezing 著者: Bauerlein FJB / Pastor-Pareja JC / Fernandez-Busnadiego R | ||||||||||||
履歴 |
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-構造の表示
ムービー |
ムービービューア |
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添付画像 |
-ダウンロードとリンク
-EMDBアーカイブ
マップデータ | emd_12729.map.gz | 254.4 MB | EMDBマップデータ形式 | |
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ヘッダ (付随情報) | emd-12729-v30.xml emd-12729.xml | 14 KB 14 KB | 表示 表示 | EMDBヘッダ |
画像 | emd_12729.png | 372.5 KB | ||
アーカイブディレクトリ | http://ftp.pdbj.org/pub/emdb/structures/EMD-12729 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-12729 | HTTPS FTP |
-検証レポート
文書・要旨 | emd_12729_validation.pdf.gz | 188.4 KB | 表示 | EMDB検証レポート |
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文書・詳細版 | emd_12729_full_validation.pdf.gz | 187.5 KB | 表示 | |
XML形式データ | emd_12729_validation.xml.gz | 3.9 KB | 表示 | |
CIF形式データ | emd_12729_validation.cif.gz | 4.4 KB | 表示 | |
アーカイブディレクトリ | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-12729 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-12729 | HTTPS FTP |
-関連構造データ
-リンク
EMDBのページ | EMDB (EBI/PDBe) / EMDataResource |
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-マップ
ファイル | ダウンロード / ファイル: emd_12729.map.gz / 形式: CCP4 / 大きさ: 328.5 MB / タイプ: IMAGE STORED AS SIGNED INTEGER (2 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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注釈 | Tomogram of a Drosophila Malpighian tubule vitrified by plunge freezing upon incubation in 10% glycerol | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
投影像・断面図 | 画像のコントロール
画像は Spider により作成 これらの図は立方格子座標系で作成されたものです | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ボクセルのサイズ | X=Y=Z: 17.56 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
密度 |
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対称性 | 空間群: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
詳細 | EMDB XML:
CCP4マップ ヘッダ情報:
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-添付データ
-試料の構成要素
-全体 : Tomogram of a Drosophila Malpighian tubule vitrified by plunge fr...
全体 | 名称: Tomogram of a Drosophila Malpighian tubule vitrified by plunge freezing upon incubation in 10% glycerol |
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要素 |
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-超分子 #1: Tomogram of a Drosophila Malpighian tubule vitrified by plunge fr...
超分子 | 名称: Tomogram of a Drosophila Malpighian tubule vitrified by plunge freezing upon incubation in 10% glycerol タイプ: tissue / ID: 1 / 親要素: 0 |
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由来(天然) | 生物種: Drosophila melanogaster (キイロショウジョウバエ) 株: wild type Canton-S strain / 器官: Malpighian tubule / 組織: Epithelial tissue |
-実験情報
-構造解析
手法 | クライオ電子顕微鏡法 |
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解析 | 電子線トモグラフィー法 |
試料の集合状態 | tissue |
-試料調製
緩衝液 | pH: 7.4 / 構成要素 - 名称: PBS |
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グリッド | モデル: Quantifoil R2/1 / 材質: MOLYBDENUM / メッシュ: 200 / 支持フィルム - 材質: CARBON / 支持フィルム - トポロジー: HOLEY |
凍結 | 凍結剤: ETHANE-PROPANE / 装置: HOMEMADE PLUNGER 詳細: The grids were mounted on a manual plunger, blotted from the back side using Whatman paper #1 (Sigma-Aldrich) and plunged into a 2:1 ethane:propane mixture cooled down by liquid nitrogen by ...詳細: The grids were mounted on a manual plunger, blotted from the back side using Whatman paper #1 (Sigma-Aldrich) and plunged into a 2:1 ethane:propane mixture cooled down by liquid nitrogen by the Martinsried-Plunger.. |
詳細 | Dissected intact Drosophila Malpighian tubules with ureter, hind- and midgut were deposited on an EM grid. |
Cryo protectant | 10% glycerol |
切片作成 | 集束イオンビーム - 装置: OTHER / 集束イオンビーム - イオン: OTHER / 集束イオンビーム - 電圧: 30 kV / 集束イオンビーム - 電流: 0.05 nA / 集束イオンビーム - 時間: 3600 sec. / 集束イオンビーム - 温度: 90 K / 集束イオンビーム - Initial thickness: 50000 nm / 集束イオンビーム - 最終 厚さ: 160 nm 集束イオンビーム - 詳細: To prepare thin electron transparent lamellae into the tissue, plunge-frozen grids were first mounted into Autogrid frames (FEI). The grids were then mounted into a ...集束イオンビーム - 詳細: To prepare thin electron transparent lamellae into the tissue, plunge-frozen grids were first mounted into Autogrid frames (FEI). The grids were then mounted into a dual-beam Quanta 3D FIB/SEM (FEI) using a custom-built transfer shuttle and a cryo-transfer system (PP3000T, Quorum). The samples were kept at -180 C throughout FIB milling by the cryo-stage. To improve SEM imaging, a thin layer of pure metallic Pt was sputtered onto the sample under cryo conditions in the PP3000T transfer system to increase its electrical conductivity. The following parameters were used: 10 mA sputtering current, 500 V between stage and sputtering target and 30 s of exposure at 4.5x10-2 mbar. To interpret and annotate the topographical anatomy of the tissue, overview maps of the EM grid were acquired by SEM at 10 kV at 100-250x magnification (object pixel size 1.1-0.4 um) and by secondary electrons induced by the Ga+ focused ion beam at 30 kV at 338x magnification (object pixel size 0.7 um). To protect the milling front of the lamellae, gaseous organic platinum was frozen on top of the grid using a gas injection system. To prevent bending of the lamella during the preparation, micro-expansion joints were milled left and right of the intended lamella preparation site. 10-20 um wide lamellae were prepared into the tissue with the ion beam at 30 kV at shallow angles (8-14 deg) in four consecutive steps: for the thicker tissue regions (e.g. VNC or skeletal muscle), the areas above and below the intended lamella were first removed with an ion beam current of 5 nA and 10 um spacing. This step was not necessary for thinner tissues such as the peripheral nerves. Further rectangular patterns were defined above and below the intended lamella with 2 um spacing for the rough milling step (ion beam current of 500-1000 pA), followed by fine milling with 800 nm spacing (100 pA) and a final polishing step down to the final lamella thickness of 100-200 nm (50 pA). To reach a uniform thickness, the lamella was tilted by +-0.5 deg and milled on each side separately with 50 pA current. The thickness of the lamella during the polishing step was assessed by SEM at 3-5 kV, 4.1 pA: the loss of charging effects in the lamella, visualized as the vanishing of bright areas, indicates a thickness <300 nm at 5 kV or <200 nm at 3 kV. Biological structures inside the lamella at the surface were imaged at each step by SEM at 2.5 kV, 4.1 pA in integration mode (64x). To reduce lamella charging during phase plate cryo-ET data acquisition, a thin layer of pure metallic Pt was sputtered onto the lamella under cryo conditions in the PP3000T transfer system with the following parameters: 5 mA sputtering current, 500 V between stage and sputtering target and 10 s of exposure at 4.5x10-2 mbar.. The value given for _emd_sectioning_focused_ion_beam.instrument is FEI Quanta 3D FIB/SEM. This is not in a list of allowed values {'DB235', 'OTHER'} so OTHER is written into the XML file. |
-電子顕微鏡法
顕微鏡 | FEI TITAN KRIOS |
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特殊光学系 | 位相板: VOLTA PHASE PLATE / エネルギーフィルター - 名称: GIF Quantum LS / エネルギーフィルター - スリット幅: 20 eV |
詳細 | Additional Volta phase plate alignment. |
撮影 | フィルム・検出器のモデル: GATAN K2 SUMMIT (4k x 4k) 検出モード: COUNTING / デジタル化 - サイズ - 横: 3868 pixel / デジタル化 - サイズ - 縦: 3868 pixel / 平均電子線量: 3.0 e/Å2 |
電子線 | 加速電圧: 300 kV / 電子線源: FIELD EMISSION GUN |
電子光学系 | 最小 デフォーカス(補正後): 0.5 µm / 照射モード: FLOOD BEAM / 撮影モード: BRIGHT FIELD / 倍率(公称値): 33000 |
試料ステージ | 試料ホルダーモデル: FEI TITAN KRIOS AUTOGRID HOLDER ホルダー冷却材: NITROGEN |
実験機器 | モデル: Titan Krios / 画像提供: FEI Company |
-画像解析
最終 再構成 | アルゴリズム: BACK PROJECTION / ソフトウェア - 名称: IMOD (ver. 4.9.0) / 使用した粒子像数: 50 |
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