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Hydrophilic trans‐Cyclooctenylated Noncanonical Amino Acids for Fast Intracellular Protein Labeling
Authors:Eszter Kozma  Dr Ivana Niki?  Dr Balázs R Varga  Iker Valle Aramburu  Jun Hee Kang  Dr Oliver T Fackler  Dr Edward A Lemke  Dr Péter Kele
Affiliation:1. Hungarian Academy of Sciences, Research Centre for Natural Sciences, Institute of Organic Chemistry, Budapest, Hungary;2. Structural and Computational Biology Unit, Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg, Germany;3. Center of Infectious Diseases, Integrative Virology, University of Heidelberg, Heidelberg, Germany
Abstract:Introduction of bioorthogonal functionalities (e.g., trans‐cyclooctene‐TCO) into a protein of interest by site‐specific genetic encoding of non‐canonical amino acids (ncAAs) creates uniquely targetable platforms for fluorescent labeling schemes in combination with tetrazine‐functionalized dyes. However, fluorescent labeling of an intracellular protein is usually compromised by high background, arising from the hydrophobicity of ncAAs; this is typically compensated for by hours‐long washout to remove excess ncAAs from the cellular interior. To overcome these problems, we designed, synthesized, and tested new, hydrophilic TCO‐ncAAs. One derivative, DOTCO‐lysine was genetically incorporated into proteins with good yield. The increased hydrophilicity shortened the excess ncAA washout time from hours to minutes, thus permitting rapid labeling and subsequent fluorescence microscopy.
Keywords:amino acids  click chemistry  fluorescence  hydrophilicity  protein engineering
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