Fluorogenic and fluorescent bioorthogonal labelling strategies for examining glycoproteins and phospholipids

• Author / Creator

  Key, Jessie Adam

• Traditional genetically-encoded imaging strategies are problematic for use in analysing cell surface interactions due to the heterogeneous nature of the cell surface, and the high level of post-translational modifications. Small molecule fluorophores can provide dynamic information on cell surface interactions due to their small size, low detection limits and environmental sensitivity. Recent advances in bioconjugate strategies such as the Staudinger ligation, Sharpless-Meldal reaction and periodate oxidation with aniline-catalyzed ligation (PAL) and hydrazone/oxime forming reactions have imparted improved specificity. However, there remains a need for chromophores with improved specificity. This thesis describes the synthesis and application of novel chromophores for cell surface imaging. We employed selective labelling strategies to combat background signal, and enable detection of specific post-translational modifications. We generated a small library of alkynyl coumarin profluorophores and characterized the corresponding alkyne and triazole derivatives. We observed increased fluorescence emission quantum yields of up to 9-fold and bathochromic shift of up to 23 nm due to the formation of the triazole linkage. Although these dyes are useful for fluorogenic labelling strategies, their relatively low brightness and short excitation wavelength inspired us to examine a new series of alkynyl and azido benzoxadiazole fluorophores for labelling cell surface glycoconjugates. We were able to identify reactive chromophores which act as fluorogenic, quenched, and static fluorescent labels. The fluorogenic dye showed an almost 50-fold increase of intensity, and the quenched dyes showed up to 500-fold loss of intensity. To quantify sialic acid content, using PAL methodology, we developed a novel 4-aminooxy-7-nitro- benzoxadiazole (NBDAO) fluorophore, and compared its performance with commercially available dyes. NBDAO was excited by a 488 nm laser line and found to be suitable for in vitro and in vivo labelling studies using SDS-PAGE, microplate assays, fluorescence spectroscopy, and flow cytometry. As well, a series of bioorthogonal cyanine-5 fluorophores and choline derivatives were synthesized and examined for suitability in phospholipid metabolic labelling experiments. Propargyl- and azido- choline readily incorporated as metabolic labels of phospholipids. However, a carbonyl-choline analog did not show any incorporation. The Cy 5 dyes were found to have exceptionally high absorption coefficients and long-wavelength absorption and emission.

• Subjects / Keywords

  • Phospholipids
  • Bioorthogonal
  • Glycoproteins
  • Fluorogenic

• Graduation date

  Fall 2012

• Type of Item

  Thesis

• Degree

  Doctor of Philosophy

• DOI

  https://doi.org/10.7939/R37W67F00

• License

  This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.