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BioID screening of biotinylation sites using the avidin-like protein Tamavidin 2-REV identifies global interactors of stimulator of interferon genes (STING)

https://tokushima-u.repo.nii.ac.jp/records/2008852
https://tokushima-u.repo.nii.ac.jp/records/2008852
6ddc5453-075f-4dea-8252-ccc94104fa70
名前 / ファイル ライセンス アクション
jbc_295_32_11174.pdf jbc_295_32_11174.pdf (2.12 MB)
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Item type 文献 / Documents(1)
公開日 2021-08-20
アクセス権
アクセス権 open access
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版社版DOI
関連識別子 https://doi.org/10.1074/jbc.ra120.014323
関連名称 10.1074/jbc.ra120.014323
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル BioID screening of biotinylation sites using the avidin-like protein Tamavidin 2-REV identifies global interactors of stimulator of interferon genes (STING)
タイトル別表記
その他のタイトル BioID using Tamavidin 2-REV
著者 茂谷, 康

× 茂谷, 康

WEKO 684
徳島大学 教育研究者総覧 276053/profile-ja.html
e-Rad 70609049

ja 茂谷, 康
ISNI

ja-Kana モタニ, コウ

en Motani, Kou

Search repository
小迫, 英尊

× 小迫, 英尊

WEKO 301
徳島大学 教育研究者総覧 172252/profile-ja.html
e-Rad 10291171

ja 小迫, 英尊
ISNI

ja-Kana コサコ, ヒデタカ

en Kosako, Hidetaka

Search repository
抄録
内容記述 Stimulator of interferon genes (STING) mediates cytosolic DNA-induced innate immune signaling via membrane trafficking. The global identification of proteins that spatiotemporally interact with STING will provide a better understanding of its trafficking mechanisms and of STING signaling pathways. Proximity-dependent biotin identification (BioID) is a powerful technology to identify physiologically relevant protein-protein interactions in living cells. However, biotinylated peptides are rarely detected in the conventional BioID method, which uses streptavidin beads to pull down biotinylated proteins, because the biotin-streptavidin interaction is too strong. As a result, only nonbiotinylated peptides are identified, which cannot be distinguished from peptides of nonspecifically pull-downed proteins. Here, we developed a simple method to efficiently and specifically enrich biotinylated peptides using Tamavidin 2-REV, an engineered avidin-like protein with reversible biotin-binding capability. Using RAW264.7 macrophages stably expressing TurboID-fused STING, we identified and quantified >4,000 biotinylated peptides of STING-proximal proteins. Various endoplasmic reticulum-associated proteins were biotinylated in unstimulated cells, and STING activation caused biotinylation of many proteins located in the Golgi and endosomes. These proteins included those known to interact with activated STING, such as TANK-binding kinase 1 (TBK1), several palmitoyl transferases, and p62/sequestosome 1 (SQSTM1). Furthermore, interferon-induced transmembrane protein 3 (IFITM3), an endolysosome-localized antiviral protein, bound to STING at the late activation stage. These dynamic interaction profiles will provide detailed insights into STING signaling; we propose that our approach using Tamavidin 2-REV would be useful for BioID-based and other biotinylation-based peptide identification methods.
書誌情報 en : Journal of Biological Chemistry

巻 295, 号 32, p. 11174-11183, 発行日 2020-06-17
収録物ID
収録物識別子タイプ ISSN
収録物識別子 00219258
収録物ID
収録物識別子タイプ NCID
収録物識別子 AA1202441X
出版者
出版者 American Society for Biochemistry and Molecular Biology
出版者
出版者 Elsevier
権利情報
権利情報 This is an Open Access article under the CC BY license.
EID
識別子 366538
言語
言語 eng
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