Fluorescent labeling of biomolecules with organic probes

M. Sameiro*, T. Gonçalves

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    1020 Scopus citations

    Abstract

    An insight into the field of the synthesis and application of organic fluorescent markers for labeling of amino acids, peptides, proteins, DNA, and other biomolecules, is provided. The carboxylic benzofuran and naphthofuran derivatives are used in the derivatization of α-amino acids located in the amine function of their main or lateral chains and in the hydroxyl group of the lateral chain. 4,7-phenanthroline-5,6-dione are used as a fluorogenic labeling reagent in precolumn derivatization for the liquid chromatography (LC) separation of amino acids. Studies have shown that the uncaging of 1-(2-nitrophenyl)ethyl phosphoserine peptide is used to release bioactive species. Fluorescent labeling technologies such as the fluorescent biarsenical dye molecules are desirable in the use of large fusion proteins.

    Original languageEnglish (US)
    Pages (from-to)190-212
    Number of pages23
    JournalCHEMICAL REVIEWS
    Volume109
    Issue number1
    DOIs
    StatePublished - Jan 14 2009

    ASJC Scopus subject areas

    • General Chemistry

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