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  1. 原著論文

Using the QCM Biosensor-Based T7 Phage Display Combined with Bioinformatics Analysis for Target Identification of Bioactive Small Molecule

https://repo.qst.go.jp/records/49395
https://repo.qst.go.jp/records/49395
731ed097-8c9d-499a-ac6c-6f34f7497de8
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-06-04
タイトル
タイトル Using the QCM Biosensor-Based T7 Phage Display Combined with Bioinformatics Analysis for Target Identification of Bioactive Small Molecule
言語
言語 eng
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
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Takakusagi, Yoichi

× Takakusagi, Yoichi

WEKO 748166

Takakusagi, Yoichi

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Takakusagi, Kaori

× Takakusagi, Kaori

WEKO 748167

Takakusagi, Kaori

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Sugawara, Fumio

× Sugawara, Fumio

WEKO 748168

Sugawara, Fumio

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Sakaguchi, Kengo

× Sakaguchi, Kengo

WEKO 748169

Sakaguchi, Kengo

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Takakusagi, Yoichi

× Takakusagi, Yoichi

WEKO 748170

en Takakusagi, Yoichi

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Takakusagi, Kaori

× Takakusagi, Kaori

WEKO 748171

en Takakusagi, Kaori

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抄録
内容記述タイプ Abstract
内容記述 Identification of target proteins that directly bind to bioactive small molecule is of great interest in terms of clarifying the mode of action of the small molecule as well as elucidating the biological phenomena at the molecular level. Of the experimental technologies available, T7 phage display allows comprehensive screening of small molecule-recognizing amino acid sequence from the peptide libraries displayed on the T7 phage capsid. Here, we describe the T7 phage display strategy that is combined with quartz-crystal microbalance (QCM) biosensor for affinity selection platform and bioinformatics analysis for small molecule-recognizing short peptides. This method dramatically enhances efficacy and throughput of the screening for small molecule-recognizing amino acid sequences without repeated rounds of selection. Subsequent execution of bioinformatics programs allows combinatorial and comprehensive target protein discovery of small molecules with its binding site, regardless of protein sample insolubility, instability, or inaccessibility of the fixed small molecules to internally located binding site on larger target proteins when conventional proteomics approaches are used.
書誌情報 Methods Mol Biol

巻 1795, p. 159-172, 発行日 2018-05
出版者
出版者 Springer Protocols
ISSN
収録物識別子タイプ ISSN
収録物識別子 1064-3745
PubMed番号
識別子タイプ PMID
関連識別子 29846927
DOI
識別子タイプ DOI
関連識別子 10.1007/978-1-4939-7874-8_14
関連サイト
識別子タイプ URI
関連識別子 http://www.bookmetrix.com/detail/chapter/ce268f1a-89eb-4439-9536-4a29c74d5cda#downloads
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