Ratiometric imaging of minor groove binders in mammalian cells using Raman microscopy

Tentellino, Christian and Tipping, William J. and McGee, Leah M. C. and Bain, Laura M. and Wetherill, Corinna and Laing, Stacey and Tyson-Hirst, Izaak and Suckling, Colin J. and Beveridge, Rebecca and Scott, Fraser J. and Faulds, Karen and Graham, Duncan (2022) Ratiometric imaging of minor groove binders in mammalian cells using Raman microscopy. RSC Chemical Biology, 3 (12). pp. 1403-1415. ISSN 2633-0679 (https://doi.org/10.1039/D2CB00159D)

[thumbnail of Tentellino-etal-RSCCB-2022-Ratiometric-imaging-of-minor-groove-binders-in-mammalian-cells-using-Raman-microscopy]
Preview
 Text. Filename: Tentellino_etal_RSCCB_2022_Ratiometric_imaging_of_minor_groove_binders_in_mammalian_cells_using_Raman_microscopy.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (2MB)| Preview

Abstract

Quantitative drug imaging in live cells is a major challenge in drug discovery and development. Many drug screening techniques are performed in solution, and therefore do not consider the impact of the complex cellular environment in their result. As such, important features of drug-cell interactions may be overlooked. In this study, Raman microscopy is used as a powerful technique for semi-quantitative imaging of Strathclyde-minor groove binders (S-MGBs) in mammalian cells under biocompatible imaging conditions. Raman imaging determined the influence of the tail group of two novel minor groove binders (S-MGB-528 and S-MGB-529) in mammalian cell models. These novel S-MGBs contained alkyne moieties which enabled analysis in the cell-silent region of the Raman spectrum. The intracellular uptake concentration, distribution and mechanism were evaluated as a function of the pKa of the tail group, morpholine and amidine, for S-MGB-528 and S-MGB-529, respectively. Although S-MGB-529 had a higher binding affinity to the minor groove of DNA in solution-phase measurements, the Raman imaging data indicated that S-MGB-528 showed a greater degree of intracellular accumulation. Furthermore, using high resolution stimulated Raman scattering (SRS) microscopy, the initial localisation of S-MGB-528 was shown to be in the nucleus before accumulation in the lysosome, which was demonstrated using a multimodal imaging approach. This study highlights the potential of Raman spectroscopy for semi-quantitative drug imaging studies and highlights the importance of imaging techniques to investigate drug-cell interactions, to better inform the drug design process.

ORCID iDs

Tentellino, Christian, Tipping, William J., McGee, Leah M. C. ORCID logoORCID: https://orcid.org/0000-0002-9896-0450, Bain, Laura M., Wetherill, Corinna ORCID logoORCID: https://orcid.org/0000-0001-7263-1352, Laing, Stacey ORCID logoORCID: https://orcid.org/0000-0001-5781-349X, Tyson-Hirst, Izaak, Suckling, Colin J., Beveridge, Rebecca ORCID logoORCID: https://orcid.org/0000-0003-0320-6496, Scott, Fraser J. ORCID logoORCID: https://orcid.org/0000-0003-0229-3698, Faulds, Karen ORCID logoORCID: https://orcid.org/0000-0002-5567-7399 and Graham, Duncan ORCID logoORCID: https://orcid.org/0000-0002-6079-2105;
CORE (COnnecting REpositories)