A robust split-luciferase-based cell fusion screening for discovering myogenesis-promoting molecules
文献情報
Qiaojing Li, Hideaki Yoshimura, Maki Komiya, Ken Tajiri, Motonari Uesugi, Yutaka Hata, Takeaki Ozawa
Myogenesis-promoting chemicals are an important source of new pharmaceuticals for the treatment of skeletal muscle atrophy that impairs quality of life. This report presents a robust and quantitative bioluminescence-based assay for screening myogenesis-promoting compounds in chemical libraries. The assay system consists of two stable C2C12 myoblast cell lines, each of which expresses either an N-terminal or a C-terminal split luciferase fragment fused to a naturally split DnaE intein as an indicator for cell fusion. Cell fusion during myogenesis induces bioluminescence in the cytosol because of the reconstitution of luciferases. The luminescence intensity quantitatively represents the progress in the cell fusion and therefore indicates the extent of myogenesis. We applied this assay system to a high-throughput screening of myogenesis-promoting compouns in 1191 pharmacologically proven bioactive small molecules, which revealed two chemical compounds as myogenesis-promoting compounds: Imatinib and Doxazosin mesylate. The assay system enabled a robust and quantitative evaluation of the extent of myogenesis through simple luminescence measurements, and is expected to be widely applicable for high-throughput screening of cell fusion-promoting and inhibiting molecules.
関連文献
Synthesis and characterization of various 5′-dye-labeled ribonucleosides
Coralie De Schutter, Vincent Roy, Patrick Favetta, Corentin Pavageau, Stéphane Maisonneuve, Nicolas Bogliotti, Juan Xie, Luigi A. Agrofoglio
DOI: 10.1039/C8OB01606B
Enzymatic synthesis of base-modified RNA by T7 RNA polymerase. A systematic study and comparison of 5-substituted pyrimidine and 7-substituted 7-deazapurine nucleoside triphosphates as substrates
Pavla Perlíková, Radek Pohl
DOI: 10.1039/C8OB01498A
Palladium-catalyzed selective synthesis of 3,4-dihydroquinazolines from electron-rich arylamines, electron-poor arylamines and glyoxalates
Jie Wang, Xing-Yu Zhang, Guo-Kai Jia, Zhong Cao, Zilong Tang, Xianyong Yu, Xinhua Xu
DOI: 10.1039/C8OB01005F
Molecular engineering of logic gate types by module rearrangement in ‘Pourbaix Sensors’: the effect of excited-state electric fields
Jake C. Spiteri, Sergey A. Denisov, Gediminas Jonusauskas, Sylwia Klejna, Konrad Szaciłowski, Nathan D. McClenaghan, David C. Magri
DOI: 10.1039/C8OB00485D
Tandem radical cyclization of N-methacryloyl benzamides with CBr4 to construct brominated isoquinolinediones
Songhai Huang, Pengfei Niu, Yingpeng Su, Dongcheng Hu, Congde Huo
DOI: 10.1039/C8OB01964A
Geometric deconstruction of core and electron activation of a π-system in a series of deformed porphyrins: mimics of heme
Qiuhua Liu, Jinjin Zhang, Min Tang, Yan Yang, Jian Zhang, Zaichun Zhou
DOI: 10.1039/C8OB01959B
A red-emitting fluorescent probe for the detection of Hg2+ in aqueous medium, living cells and organisms with a large Stokes shift
Lei Yang, Yuanan Su, Yani Geng, Haiqing Xiong, Jinliang Han, Qian Fang, Xiangzhi Song
DOI: 10.1039/C8OB00831K
Novel binaphthyl and biphenyl α- and β-amino acids and esters: organocatalysis of asymmetric Diels–Alder reactions. A combined synthetic and computational study
Philip C. Bulman Page, Francesca S. Kinsey, Yohan Chan, Ian R. Strutt, Alexandra M. Z. Slawin, Garth A. Jones
DOI: 10.1039/C8OB01795F
Recent developments and applications of cyanamides in electrophilic cyanation
Manthena Chaitanya, Pazhamalai Anbarasan
DOI: 10.1039/C8OB01770K
Regioselectivity of aryl radical attack onto isocyanates and isothiocyanates
Geethika K. Weragoda, Rowan L. Pilkington, Richard A. J. O'Hair
DOI: 10.1039/C8OB02209G
こちらもおすすめ
3-イチチルビフェニルはどのように合成されますか?
3-イチチルビフェニルは、ビフェニルとイチプロピオニトリルを回収率約90%で反応させて合成されます。触媒は通常、亜リチウムホウ素を用います。
8-溴-5-三氟甲基喹啉はどのように合成されますか?
8-溴-5-三氟甲基喹啉は、5-トリフルオロメチル-2-メチル-1,3-ベンゼンジオールをブロモエタノールと反応させて生成します。この反応は塩基性条件下で行われ...
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品はありますか?
ジメチル4-(4,4,5,5-テトラメチル-1,3,2-ドioxaborolan-2-基)-2,6-ピリジンジカルボイル酸フェニルアミニドの代替品としては、4-...
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向や研究トレンドはどのようなものでしょうか?
N-(3,5-ヘキサクロロ-4-ピリドインイル)-8-メチオキシ-5-キノリンカーボン酸の市場動向は、主に産業用途での需要により影響を受けます。研究トレンドとし...
イソステアロイルグリセリルは安全ですか?
イソステアロイルグリセリルは一般的に安全性が高いとされていますが、過度な使用や個人差により皮�owsん炎などの反応が起こる可能性があります。使用前に医師に相談す...
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向や研究トレンドはどうですか?
1-(二苯甲基)-3,3-二氟-氮杂环丁烷の市場動向は、医薬品や合成化学の研究分野で注目を集めています。新興研究は、該当化合物の合成改良と生体内での作用メカニズ...
3-チオフェンスチオールの物理化学的性質は何ですか?
3-チオフェンスチオールのCAS番号は7774-73-4です。結晶性の白色粉末で、分子量は122.17です。この化合物は水に微溶解し、エタノールやジクロロメタン...
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは安全ですか?
2-Methyl-2-propanyl (2S)-2-(aminomethyl)-1-piperidinecarboxylateは一定の安全性基準を満たしていま...
CAS番号1316822-90-8の化合物は安全ですか?
CAS番号1316822-90-8の化合物は安全性に関しては評価が不足していますが、一般的には生物学的に活性な物質であり、取り扱いには適切な安全防護措置が必要で...
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸はどのように保存すればよいですか?
Tert-butyl 2-(2-羟基乙基)哌嗪-1-羧酸は、冷暗所で保存し、直射日光から遠ざけてください。容器は密閉し、高湿度や高温を避けて保管してください。
掲載誌
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.










![1-oxaspiro[4.4]nonan-6-one structure 1-oxaspiro[4.4]nonan-6-one structure](https://static.chemtradehub.com/structs/134/134179-01-4-e051.webp)

![5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure 5'-Fluoro-[2,3'-biindolinylidene]-2',3-dione structure](https://static.chemtradehub.com/structs/251/251903-00-1-9cb1.webp)

