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Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time

Author

Listed:
  • Marco Grossi

    (Royal College of Surgeons in Ireland)

  • Marina Morgunova

    (Royal College of Surgeons in Ireland)

  • Shane Cheung

    (Royal College of Surgeons in Ireland
    School of Chemistry and Chemical Biology, Conway Institute, University College Dublin)

  • Dimitri Scholz

    (School of Biomolecular and Biomedical Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin)

  • Emer Conroy

    (School of Biomolecular and Biomedical Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin)

  • Marta Terrile

    (School of Biomolecular and Biomedical Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin)

  • Angela Panarella

    (School of Biology and Environmental Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin)

  • Jeremy C. Simpson

    (School of Biology and Environmental Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin)

  • William M. Gallagher

    (School of Biomolecular and Biomedical Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin)

  • Donal F. O’Shea

    (Royal College of Surgeons in Ireland
    School of Chemistry and Chemical Biology, Conway Institute, University College Dublin)

Abstract

Bioresponsive NIR-fluorophores offer the possibility for continual visualization of dynamic cellular processes with added potential for direct translation to in vivo imaging. Here we show the design, synthesis and lysosome-responsive emission properties of a new NIR fluorophore. The NIR fluorescent probe design differs from typical amine functionalized lysosomotropic stains with off/on fluorescence switching controlled by a reversible phenol/phenolate interconversion. Emission from the probe is shown to be highly selective for the lysosomes in co-imaging experiments using a HeLa cell line expressing the lysosomal-associated membrane protein 1 fused to green fluorescent protein. The responsive probe is capable of real-time continuous imaging of fundamental cellular processes such as endocytosis, lysosomal trafficking and efflux in 3D and 4D. The advantage of the NIR emission allows for direct translation to in vivo tumour imaging, which is successfully demonstrated using an MDA-MB-231 subcutaneous tumour model. This bioresponsive NIR fluorophore offers significant potential for use in live cellular and in vivo imaging, for which currently there is a deficit of suitable molecular fluorescent tools.

Suggested Citation

  • Marco Grossi & Marina Morgunova & Shane Cheung & Dimitri Scholz & Emer Conroy & Marta Terrile & Angela Panarella & Jeremy C. Simpson & William M. Gallagher & Donal F. O’Shea, 2016. "Lysosome triggered near-infrared fluorescence imaging of cellular trafficking processes in real time," Nature Communications, Nature, vol. 7(1), pages 1-13, April.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10855
    DOI: 10.1038/ncomms10855
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