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PMID: 7573951 Published · ppublish English Journal Article

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

Analytical biochemistry ·Vol. 227 ·No. 2 ·1995-05-20 ·Pages 302-8

Sanders R, Draaijer A, Gerritsen HC, Houpt PM, Levine YK

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.

MeSH Terms
Animals Buffers CHO Cells Calibration Cells/chemistry Cricetinae Hydrogen-Ion Concentration Microscopy, Confocal Microscopy, Fluorescence/methods Proteins/chemistry Sensitivity and Specificity Solubility Tumor Cells, Cultured Water/chemistry
Chemicals
Buffers Proteins Water
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Sanders R
Department of Molecular Biophysics, Debye Institute, University of Utrecht, Buys Ballot Laboratory, The Netherlands.
Draaijer A
Gerritsen H C
Houpt P M
Levine Y K
Article Info
Journal
Analytical biochemistry
Abbr.
Anal Biochem
ISSN
0003-2697
Published
1995-05-20
Pages
302-8
Language
English
Region
United States
NLM ID
0370535
Subset
IM
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