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Easy-to-Attach/Detach Solubilizing-Tag-Aided Chemical Synthesis of an Aggregative Capsid Protein.
Tsuda, Shugo; Mochizuki, Masayoshi; Ishiba, Hiroyuki; Yoshizawa-Kumagaye, Kumiko; Nishio, Hideki; Oishi, Shinya; Yoshiya, Taku.
Afiliação
  • Tsuda S; Peptide Institute, Inc., Ibaraki, Osaka, 567-0085, Japan.
  • Mochizuki M; Peptide Institute, Inc., Ibaraki, Osaka, 567-0085, Japan.
  • Ishiba H; Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, 606-8501, Japan.
  • Yoshizawa-Kumagaye K; Peptide Institute, Inc., Ibaraki, Osaka, 567-0085, Japan.
  • Nishio H; Graduate School of Science, Osaka University, Toyonaka-shi, Osaka, 560-0043, Japan.
  • Oishi S; Peptide Institute, Inc., Ibaraki, Osaka, 567-0085, Japan.
  • Yoshiya T; Graduate School of Science, Osaka University, Toyonaka-shi, Osaka, 560-0043, Japan.
Angew Chem Int Ed Engl ; 57(8): 2105-2109, 2018 02 19.
Article em En | MEDLINE | ID: mdl-29316103
ABSTRACT
A solubilizing Trt-K10 tag was developed for the effective chemical preparation of peptides/proteins with low solubility. The Trt-K10 tag comprises a hydrophilic oligo-Lys sequence and a trityl anchor, and can be selectively introduced to a side chain thiol of Cys of deprotected peptides/proteins with a trityl alcohol-type introducing reagent Trt(OH)-K10 under acidic conditions. Significantly, the ligation product in the reaction mixture of a thiol-additive-free native chemical ligation can be modified directly in a one-pot manner to facilitate the isolation of the product by high-performance liquid chromatography. Finally, the Trt-K10 tag can be readily removed with a standard trifluoroacetic acid cocktail. Using this easy-to-attach/detach tag-aided method, a hepatitis B virus capsid protein that is usually difficult to handle was synthesized successfully.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Capsídeo Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas do Capsídeo Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão
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