| Literature DB >> 29316103 |
Shugo Tsuda1, Masayoshi Mochizuki1, Hiroyuki Ishiba2, Kumiko Yoshizawa-Kumagaye1,3, Hideki Nishio1,3, Shinya Oishi2, Taku Yoshiya1.
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.Entities:
Keywords: Trt-K10; capsid proteins; native chemical ligation; peptide synthesis; solubilizing tags
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Year: 2018 PMID: 29316103 DOI: 10.1002/anie.201711546
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336