Detection of very low receptor numbers on cells by flow cytometry using a sensitive staining method
Article first published online: 8 MAR 2005
Copyright © 1987 Wiley-Liss, Inc.
Volume 8, Issue 6, pages 562–567, November 1987
How to Cite
Truneh, A. and Machy, P. (1987), Detection of very low receptor numbers on cells by flow cytometry using a sensitive staining method. Cytometry, 8: 562–567. doi: 10.1002/cyto.990080605
- Issue published online: 16 JUN 2005
- Article first published online: 8 MAR 2005
- Manuscript Accepted: 8 JUN 1987
- Manuscript Received: 26 JAN 1987
- targeted liposomes;
- monoclonal antibodies;
- surface phenotyping
We describe a staining method for flow cytometry that resolves with a high degree of sensitivity very low numbers of cell surface molecules, which are normally too few to detect using the conventional fluorescein-conjugated reagents. We took advantage of the fact that liposomes can be constructed to contain hundreds of thousands of fluorochrome molecules per vesicle; antigen specificity can be conferred by covalently conjugating them to antibodies or protein A. Unlike fluorochromes such as fluorescein isothiocyanate (FITC) that are directly conjugated to protein ligands with a fluorochrome to protein ratio of about 2 to 1 on the average, their large encapsulating capacity gives liposomes a tremendous potential for signal amplification. In an indirect immunofluorescence study using liposomes that contained the fluorochrome carboxyfluorescein (CF) and that were covalently conjugated to protein A, we were able to obtain up to 50 times the fluorescence signal over background that could be detected with FITC-conjugated protein A. Scatchard analysis showed that the thymoma cell line RDM4 expresses 23,000 and 2,600 binding sites for monoclonal antibodies (mAb) against H-2K and H-2D, respectively. When RDM4 cells were treated with anti-H-2K mAb followed by FITC-conjugated protein A, at best we were able to obtain a fluorescence signal that was only 7 times above background. However, when these cells were treated with the same antibody followed by protein A conjugated to small unilamellar liposomes or large unilamellar liposomes, the fluorescence signals were 110 and 335 times above background, respectively. Using the liposome conjugates, we were also able to detect with ease the 2,600 binding sites for the anti-H-2D mAb, whereas the FITC conjugate failed completely to resolve specific binding from background. We estimate conservatively that by using this methodology, it will be possible to detect as few as 800 binding sites percell.