Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1982 Jun 1;93(3):981–986. doi: 10.1083/jcb.93.3.981

Fluorescent phycobiliprotein conjugates for analyses of cells and molecules

PMCID: PMC2112146  PMID: 6749865

Abstract

The synthesis of a novel class of reagents for fluorescence analyses of molecules and cells is reported. These compounds consist of a highly fluorescent phycobiliprotein conjugated to a molecule having biological specificity. Phycoerythrin-immunoglobulin, phycoerythrin-protein A, and phycoerythrin-avidin conjugates were prepared. These conjugates bind specifically to beads containing a covalently attached target molecule and render them highly fluorescent. Femtomole (10(-15) mole) quantities of phycoerythrin conjugates can be detected because of the high extinction coefficient (epsilon M = 2.4 x 10(6) cm-1 M-1 for 2.4 x 10(5) daltons) and high fluorescence quantum yield (Q = 0.8) of the phycobiliprotein moiety. An important feature of these conjugates is that they emit in the orange-red spectral region, where background fluorescence is less than at shorter wavelengths. Phycoerythrin conjugates are well-suited for two-color flow cytofluorimetric analyses employing a single excitation line. The distributions of Leu antigens (also called OKT antigens) on the surface of T-lymphocytes were analyzed using fluoresceinated antibody as the green-fluorescent stain and biotinylated antibody counter-stained with phycoerythrin-avidin as the red one. This one-laser two-color analysis showed that cells express Leu-3a and Leu-3b or neither antigen. In contrast, the distributions of Leu-2a (a marker of suppressor and cytotoxic T-cells) and Leu-3a (a marker of helper and inducer T-cells) are mutually exclusive. These studies show that phycobiliprotein conjugates can be applied to fluorescence-activated cell sorting and analysis, fluorescence microscopy, and fluorescence immunoassay.

Full Text

The Full Text of this article is available as a PDF (679.1 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bryant D. A., Glazer A. N., Eiserling F. A. Characterization and structural properties of the major biliproteins of Anabaena sp. Arch Microbiol. 1976 Oct 11;110(1):61–75. doi: 10.1007/BF00416970. [DOI] [PubMed] [Google Scholar]
  2. Carlsson J., Drevin H., Axén R. Protein thiolation and reversible protein-protein conjugation. N-Succinimidyl 3-(2-pyridyldithio)propionate, a new heterobifunctional reagent. Biochem J. 1978 Sep 1;173(3):723–737. doi: 10.1042/bj1730723. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cohen-Bazire G., Béguin S., Rimon S., Glazer A. N., Brown D. M. Physico-chemical and immunological properties of allophycocyanins. Arch Microbiol. 1977 Jan 11;111(3):225–238. doi: 10.1007/BF00549359. [DOI] [PubMed] [Google Scholar]
  4. Dale R. E., Teale F. W. Number and distribution of chromophore types in native phycobiliproteins. Photochem Photobiol. 1970 Aug;12(2):99–117. doi: 10.1111/j.1751-1097.1970.tb06044.x. [DOI] [PubMed] [Google Scholar]
  5. Deisenhofer J. Crystallographic refinement and atomic models of a human Fc fragment and its complex with fragment B of protein A from Staphylococcus aureus at 2.9- and 2.8-A resolution. Biochemistry. 1981 Apr 28;20(9):2361–2370. [PubMed] [Google Scholar]
  6. Evans R. L., Wall D. W., Platsoucas C. D., Siegal F. P., Fikrig S. M., Testa C. M., Good R. A. Thymus-dependent membrane antigens in man: inhibition of cell-mediated lympholysis by monoclonal antibodies to TH2 antigen. Proc Natl Acad Sci U S A. 1981 Jan;78(1):544–548. doi: 10.1073/pnas.78.1.544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Glazer A. N., Fang S., Brown D. M. Spectroscopic properties of C-phycocyanin and of its alpha and beta subunits. J Biol Chem. 1973 Aug 25;248(16):5679–5685. [PubMed] [Google Scholar]
  8. Glazer A. N., Fang S. Chromophore content of blue-green algal phycobiliproteins. J Biol Chem. 1973 Jan 25;248(2):659–662. [PubMed] [Google Scholar]
  9. Glazer A. N., Hixson C. S. Subunit structure and chromophore composition of rhodophytan phycoerythrins. Porphyridium cruentum B-phycoerythrin and b-phycoerythrin. J Biol Chem. 1977 Jan 10;252(1):32–42. [PubMed] [Google Scholar]
  10. Glazer A. N. Structure and molecular organization of the photosynthetic accessory pigments of cyanobacteria and red algae. Mol Cell Biochem. 1977 Dec 29;18(2-3):125–140. doi: 10.1007/BF00280278. [DOI] [PubMed] [Google Scholar]
  11. Green N. M. Avidin. Adv Protein Chem. 1975;29:85–133. doi: 10.1016/s0065-3233(08)60411-8. [DOI] [PubMed] [Google Scholar]
  12. Heitzmann H., Richards F. M. Use of the avidin-biotin complex for specific staining of biological membranes in electron microscopy. Proc Natl Acad Sci U S A. 1974 Sep;71(9):3537–3541. doi: 10.1073/pnas.71.9.3537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jue R., Lambert J. M., Pierce L. R., Traut R. R. Addition of sulfhydryl groups to Escherichia coli ribosomes by protein modification with 2-iminothiolane (methyl 4-mercaptobutyrimidate). Biochemistry. 1978 Dec 12;17(25):5399–5406. doi: 10.1021/bi00618a013. [DOI] [PubMed] [Google Scholar]
  14. Koppel D. E., Axelrod D., Schlessinger J., Elson E. L., Webb W. W. Dynamics of fluorescence marker concentration as a probe of mobility. Biophys J. 1976 Nov;16(11):1315–1329. doi: 10.1016/S0006-3495(76)85776-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ledbetter J. A., Evans R. L., Lipinski M., Cunningham-Rundles C., Good R. A., Herzenberg L. A. Evolutionary conservation of surface molecules that distinguish T lymphocyte helper/inducer and cytotoxic/suppressor subpopulations in mouse and man. J Exp Med. 1981 Feb 1;153(2):310–323. doi: 10.1084/jem.153.2.310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ledbetter J. A., Rouse R. V., Micklem H. S., Herzenberg L. A. T cell subsets defined by expression of Lyt-1,2,3 and Thy-1 antigens. Two-parameter immunofluorescence and cytotoxicity analysis with monoclonal antibodies modifies current views. J Exp Med. 1980 Aug 1;152(2):280–295. doi: 10.1084/jem.152.2.280. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Loken M. R., Parks D. R., Herzenberg L. A. Two-color immunofluorescence using a fluorescence-activated cell sorter. J Histochem Cytochem. 1977 Jul;25(7):899–907. doi: 10.1177/25.7.330738. [DOI] [PubMed] [Google Scholar]
  18. Mota G., Gheţie V., Sjöquist J. Characterization of the soluble complex formed by reacting rabbit IgG with protein A of S. aureus. Immunochemistry. 1978 Sep;15(9):639–642. doi: 10.1016/0161-5890(78)90037-8. [DOI] [PubMed] [Google Scholar]
  19. Oi V. T., Bryan V. M., Herzenberg L. A., Herzenberg L. A. Lymphocyte membrane IgG and secreted IgG are structurally and allotypically distinct. J Exp Med. 1980 May 1;151(5):1260–1274. doi: 10.1084/jem.151.5.1260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Oi V. T., Herzenberg L. A. Localization of murine Ig-1b and Ig-1a (IgG 2a) allotypic determinants detected with monoclonal antibodies. Mol Immunol. 1979 Dec;16(12):1005–1017. doi: 10.1016/0161-5890(79)90034-8. [DOI] [PubMed] [Google Scholar]
  21. Reinherz E. L., Kung P. C., Goldstein G., Schlossman S. F. Separation of functional subsets of human T cells by a monoclonal antibody. Proc Natl Acad Sci U S A. 1979 Aug;76(8):4061–4065. doi: 10.1073/pnas.76.8.4061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Schlessinger J., Shechter Y., Willingham M. C., Pastan I. Direct visualization of binding, aggregation, and internalization of insulin and epidermal growth factor on living fibroblastic cells. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2659–2663. doi: 10.1073/pnas.75.6.2659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Taylor D. L., Wang Y. L. Fluorescently labelled molecules as probes of the structure and function of living cells. Nature. 1980 Apr 3;284(5755):405–410. doi: 10.1038/284405a0. [DOI] [PubMed] [Google Scholar]
  24. Terhorst C., van Agthoven A., Reinherz E., Schlossman S. Biochemical analysis of human T lymphocyte differentiation antigens T4 and T5. Science. 1980 Jul 25;209(4455):520–521. doi: 10.1126/science.6967228. [DOI] [PubMed] [Google Scholar]
  25. Yu M. H., Glazer A. N., Spencer K. G., West J. A. Phycoerythrins of the Red Alga Callithamnion: VARIATION IN PHYCOERYTHROBILIN AND PHYCOUROBILIN CONTENT. Plant Physiol. 1981 Aug;68(2):482–488. doi: 10.1104/pp.68.2.482. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES