TY - JOUR
T1 - A ratiometric optical imaging probe for intracellular pH based on modulation of europium emission
AU - Pal, Robert
AU - Parker, David
N1 - We thank the EC networks of excellence, EMIL (503659) and DIMI (512146). Elizabeth New for the toxicity assay work and the Royal Society for support
Publisher Copyright:
© The Royal Society of Chemistry 2008
PY - 2008/2/19
Y1 - 2008/2/19
N2 - A set of three pH-responsive ratiometric Eu(iii)complexes has been synthesised incorporating a coordinated azathioxanthone sensitiser and a pH dependent alkylsulfonamide moiety. Emission properties, anion binding affinities, pH response curves and protein binding constants were studied in detail in aqueous media, and solutions containing various concentrations of interfering anions and protein were also examined. The complex, [EuL 3] exhibited some interference from protein and endogenous anions, e.g. lactate and hydrogen carbonate, but possessed a protonation constant of 7.2 in human serum solution. A suitable calibration curve was obtained and was used to determine the local pH using a 680/589 nm intensity ratio vs. pH plot. Confocal fluorescence microscopy images revealed fast uptake of the complex and a well distributed localisation within the cell; fast egress also occurred. Ribosomal localisation, with a high concentration within the protein-dense nucleoli was observed, in a similar manner to structurally related complexes bearing the same coordinated sensitising moiety. An IC50 value of 67 (±20) μM was estimated using an MTT assay. Selected emission band ratio versus pH plots allow pH measurement in the range 6 to 8, enabling intracellular pH to be measured by microscopy. A value of 7.4 was estimated for NIH 3T3 cells in the protein rich regions of the nucleolus and ribosomes.
AB - A set of three pH-responsive ratiometric Eu(iii)complexes has been synthesised incorporating a coordinated azathioxanthone sensitiser and a pH dependent alkylsulfonamide moiety. Emission properties, anion binding affinities, pH response curves and protein binding constants were studied in detail in aqueous media, and solutions containing various concentrations of interfering anions and protein were also examined. The complex, [EuL 3] exhibited some interference from protein and endogenous anions, e.g. lactate and hydrogen carbonate, but possessed a protonation constant of 7.2 in human serum solution. A suitable calibration curve was obtained and was used to determine the local pH using a 680/589 nm intensity ratio vs. pH plot. Confocal fluorescence microscopy images revealed fast uptake of the complex and a well distributed localisation within the cell; fast egress also occurred. Ribosomal localisation, with a high concentration within the protein-dense nucleoli was observed, in a similar manner to structurally related complexes bearing the same coordinated sensitising moiety. An IC50 value of 67 (±20) μM was estimated using an MTT assay. Selected emission band ratio versus pH plots allow pH measurement in the range 6 to 8, enabling intracellular pH to be measured by microscopy. A value of 7.4 was estimated for NIH 3T3 cells in the protein rich regions of the nucleolus and ribosomes.
UR - https://www.scopus.com/pages/publications/44949131451
UR - https://pubs.rsc.org/en/content/articlelanding/2008/ob/b718993a
U2 - 10.1039/b718993a
DO - 10.1039/b718993a
M3 - Journal article
C2 - 18327327
AN - SCOPUS:44949131451
SN - 1477-0520
VL - 6
SP - 1020
EP - 1033
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
IS - 6
ER -