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https://doi.org/10.1371/journal.pone.0141918
Title: | Tetrazine-containing amino acid for peptide modification and live cell labeling | Authors: | Ni Z. Zhou L. Li X. Zhang J. Dong S. |
Keywords: | 3 (4 (1, 2, 4, 5 tetrazine 3 yl) phenyl) 2 aminopropanoic acid 3 (4 benzylamino) 1, 2, 4, 5 tetrazine amino acid derivative phenylalanine derivative tetrazine derivative tyrosine derivative unclassified drug amino acid peptide fragment phenylalanine single heterocyclic rings tetrazine dye 10 A549 cell line Article biological activity cell labeling controlled study decomposition drug purity drug stability human human cell in vitro study intestine contraction kinetics mouse nonhuman peptide synthesis protein modification room temperature small intestine solubility analogs and derivatives animal chemistry intestine lung tumor male metabolism pathology tissue distribution tumor cell culture Amino Acids Animals Heterocyclic Compounds, 1-Ring Humans Intestines Lung Neoplasms Male Mice Peptide Fragments Phenylalanine Tissue Distribution Tumor Cells, Cultured |
Issue Date: | 2015 | Citation: | Ni Z., Zhou L., Li X., Zhang J., Dong S. (2015). Tetrazine-containing amino acid for peptide modification and live cell labeling. PLoS ONE 10 (11) : 141918. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0141918 | Rights: | Attribution 4.0 International | Abstract: | A novel amino acid derivative 3-(4-(1, 2, 4, 5-tetrazine-3-yl) phenyl)-2-aminopropanoic acid was synthesized in this study. The compound possessed better water-solubility and was synthesizedmore easily compared with the well-known and commercially available 3-(p-benzylamino)- 1, 2, 4, 5-tetrazine. Tetrazine-containing amino acid showed excellent stability in biologicalmedia andmight be used for cancer cell labeling. Moreover, the compound remained relatively stable in 50% TFA/DCM with little decomposition after prolonged exposure at room temperature. The compound could be utilized as phenylalanine or tyrosine analogue in peptide modification, and the tetrazine-containing peptide demonstrated more significant biological activity than that of the parent peptide. The combination of tetrazine group and amino acid offered broad development prospects of the bioorthogonal labeling and peptide synthesis. � 2015 Ni et al. | Source Title: | PLoS ONE | URI: | https://scholarbank.nus.edu.sg/handle/10635/161602 | ISSN: | 19326203 | DOI: | 10.1371/journal.pone.0141918 | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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