このアイテムのアクセス数: 90
このアイテムのファイル:
ファイル | 記述 | サイズ | フォーマット | |
---|---|---|---|---|
journal.pcbi.1009215.pdf | 3.12 MB | Adobe PDF | 見る/開く |
完全メタデータレコード
DCフィールド | 値 | 言語 |
---|---|---|
dc.contributor.author | Niina, Toru | en |
dc.contributor.author | Matsunaga, Yasuhiro | en |
dc.contributor.author | Takada, Shoji | en |
dc.contributor.alternative | 新稲, 亮 | ja |
dc.contributor.alternative | 高田, 彰二 | ja |
dc.date.accessioned | 2022-10-12T01:39:35Z | - |
dc.date.available | 2022-10-12T01:39:35Z | - |
dc.date.issued | 2021-07 | - |
dc.identifier.uri | http://hdl.handle.net/2433/276671 | - |
dc.description.abstract | Atomic force microscopy (AFM) can visualize functional biomolecules near the physiological condition, but the observed data are limited to the surface height of specimens. Since the AFM images highly depend on the probe tip shape, for successful inference of molecular structures from the measurement, the knowledge of the probe shape is required, but is often missing. Here, we developed a method of the rigid-body fitting to AFM images, which simultaneously finds the shape of the probe tip and the placement of the molecular structure via an exhaustive search. First, we examined four similarity scores via twin-experiments for four test proteins, finding that the cosine similarity score generally worked best, whereas the pixel-RMSD and the correlation coefficient were also useful. We then applied the method to two experimental high-speed-AFM images inferring the probe shape and the molecular placement. The results suggest that the appropriate similarity score can differ between target systems. For an actin filament image, the cosine similarity apparently worked best. For an image of the flagellar protein FlhAC, we found the correlation coefficient gave better results. This difference may partly be attributed to the flexibility in the target molecule, ignored in the rigid-body fitting. The inferred tip shape and placement results can be further refined by other methods, such as the flexible fitting molecular dynamics simulations. The developed software is publicly available. | en |
dc.language.iso | eng | - |
dc.publisher | Public Library of Science (PLoS) | en |
dc.rights | © 2021 Niina et al. | en |
dc.rights | This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | Cosine similarity | en |
dc.subject | Actin filaments | en |
dc.subject | Atomic force microscopy | en |
dc.subject | Dyneins | en |
dc.subject | Molecular structure | en |
dc.subject | Monomers | en |
dc.subject | Twins | en |
dc.subject | Myosins | en |
dc.title | Rigid-body fitting to atomic force microscopy images for inferring probe shape and biomolecular structure | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | PLoS Computational Biology | en |
dc.identifier.volume | 17 | - |
dc.identifier.issue | 7 | - |
dc.relation.doi | 10.1371/journal.pcbi.1009215 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | e1009215 | - |
dc.identifier.pmid | 34283829 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 19J14515 | - |
datacite.awardNumber.uri | https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-19J14515/ | - |
dc.identifier.pissn | 1553-734X | - |
dc.identifier.eissn | 1553-7358 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.awardTitle | 化学反応を可能にする粗視化分子動力学技法の開発とその転写システムへの応用 | ja |
出現コレクション: | 学術雑誌掲載論文等 |

このアイテムは次のライセンスが設定されています: クリエイティブ・コモンズ・ライセンス