Quantitative pH imaging in cells using confocal fluorescence lifetime imaging microscopy.

R Sanders; A Draaijer; H C Gerritsen; P M Houpt; Y K Levine

doi:10.1006/abio.1995.1285

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Quantitative pH imaging in cells using confocal fluorescence lifetime imaging microscopy.

R Sanders·A Draaijer·H C Gerritsen·P M Houpt·Y K Levine

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Abstract

The pH-sensitive probe carboxy SNAFL-1 can be used for imaging using ratiometric and fluorescence lifetime techniques. The former method suffers from the drawback that quantitative pH imaging in cells requires a time-consuming and cumbersome calibration procedure. In contrast, straightforward calibrations in buffer suffice for fluorescence lifetime imaging. This is illustrated here by a comparative study of the two techniques under different controlled conditions. The effect of probe concentration, protein concentration, and hydrophobicity, the contents of damaged cells and living cells on the emission ratio, and the fluorescence lifetime of carboxy SNAFL-1 were studied. The results clearly demonstrate that the fluorescence lifetime imaging technique is more convenient than the ratiometric method for pH determination.

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Animals Buffers CHO Cells Calibration Cells Cricetinae Hydrogen-Ion Concentration Microscopy, Confocal Microscopy, Fluorescence Proteins Sensitivity and Specificity Solubility Tumor Cells, Cultured Water Journal Article

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R Sanders, A Draaijer, H C Gerritsen, P M Houpt, Y K Levine. 1995-05-20. Quantitative pH imaging in cells using confocal fluorescence lifetime imaging microscopy.. https://doi.org/10.1006/abio.1995.1285

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