Please use this identifier to cite or link to this item: 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
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