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. 1972 Oct 1;136(4):907–930. doi: 10.1084/jem.136.4.907

LIGAND-INDUCED MOVEMENT OF LYMPHOCYTE MEMBRANE MACROMOLECITLES

II. MAPPING OF SURFACE MOIETIES

Morris J Karnovsky 1, Emil R Unanue 1, Monika Leventhal 1
PMCID: PMC2139269  PMID: 5056672

Abstract

Anti-immunoglobulin (Ig) coupled to ferritin or hemocyanin was used to map the distribution of Ig molecules on lymphocytes derived from bone marrow (B lymphocytes) by freeze-etching. The labeled anti-Ig was distributed all over the membrane in the form of random interconnected patches forming a lacy, continuous network. This was the pattern of lymphocytes labeled at 4°C with the anti-Ig. After warming at 37°C, the labeled molecules concentrated into a single area of the cell (forming the cap) and were rapidly internalized in small vesicles Freeze-etching showed close packing of the labeled molecules in the cap area. There was evidence that in the cap area the Ig molecules were exfoliated from the plane of the membrane, suggesting that the Ig may be superficial to the bilipid layer, or weakly anchored to the membrane. Similar studies were made using antibodies to histocompatibility antigens. Thymocytes were labeled with anti-H-2 and ferritin anti-Ig at 4°C. Freeze-etching showed large patches scattered over the membrane and separated from each other by several thousand angstroms. This distribution may, in part, explain why H-2 antigens do not readily form a cap; the large patches are beyond the reach of even a double ligand (sandwich) reaction. The antigens that reacted with heterologous anti-lymphocyte globulin (ALG) were found in small noninterconnected clusters a few hundred angstroms apart. Such clusters presumably cannot be linked by a single antibody but can by a sandwich (ligand to ligand-antigen) reaction. In previous studies it was found that ALG antigens form a cap only after a sandwich reaction. Finally, the receptors for concanavalin A (Con A) were found in a lacy, irregular interconnected, random network. The spatial distribution of these moieties on the membrane may, in great part, determine their movement after reaction with one or two ligands.

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Selected References

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

  1. Ainsworth S. K., Karnovsky M. J. An ultrastructural staining method for enhancing the size and electron opacity of ferritin in thin sections. J Histochem Cytochem. 1972 Mar;20(3):225–229. doi: 10.1177/20.3.225. [DOI] [PubMed] [Google Scholar]
  2. Aoki T., Hämmerling U., De Harven E., Boyse E. A., Old L. J. Antigenic structure of cell surfaces. An immunoferritin study of the occurrence and topography of H-2' theta, and TL alloantigens on mouse cells. J Exp Med. 1969 Nov 1;130(5):979–1001. doi: 10.1084/jem.130.5.979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Avrameas S. Coupling of enzymes to proteins with glutaraldehyde. Use of the conjugates for the detection of antigens and antibodies. Immunochemistry. 1969 Jan;6(1):43–52. doi: 10.1016/0019-2791(69)90177-3. [DOI] [PubMed] [Google Scholar]
  4. Frye L. D., Edidin M. The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons. J Cell Sci. 1970 Sep;7(2):319–335. doi: 10.1242/jcs.7.2.319. [DOI] [PubMed] [Google Scholar]
  5. Hardman K. D., Wood M. K., Schiffer M., Edmundson A. B., Ainsworth C. F. Structure of concanavalin A at 4.25-ångström resolution. Proc Natl Acad Sci U S A. 1971 Jul;68(7):1393–1397. doi: 10.1073/pnas.68.7.1393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kourilsky F. M., Silvestre D., Neauport-Sautes C., Loosfelt Y., Dausset J. Antibody-induced redistribution of HL-A antigens at the cell surface. Eur J Immunol. 1972 Jun;2(3):249–257. doi: 10.1002/eji.1830020311. [DOI] [PubMed] [Google Scholar]
  7. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  8. Mancini G., Carbonara A. O., Heremans J. F. Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry. 1965 Sep;2(3):235–254. doi: 10.1016/0019-2791(65)90004-2. [DOI] [PubMed] [Google Scholar]
  9. Mann D. L., Fahey J. L. Histocompatibility antigens. Annu Rev Microbiol. 1971;25:679–710. doi: 10.1146/annurev.mi.25.100171.003335. [DOI] [PubMed] [Google Scholar]
  10. Nicolson G. L., Hyman R., Singer S. J. The two-dimensional topographic distribution of H-2 histocompatibility alloantigens on mouse red blood cell membranes. J Cell Biol. 1971 Sep;50(3):905–910. doi: 10.1083/jcb.50.3.905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Nicolson G. L., Singer S. J. Ferritin-conjugated plant agglutinins as specific saccharide stains for electron microscopy: application to saccharides bound to cell membranes. Proc Natl Acad Sci U S A. 1971 May;68(5):942–945. doi: 10.1073/pnas.68.5.942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Perkins W. D., Karnovsky M. J., Unanue E. R. An ultrastructural study of lymphocytes with surface-bound immunoglobulin. J Exp Med. 1972 Feb 1;135(2):267–276. doi: 10.1084/jem.135.2.267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Quiocho F. A., Reeke G. N., Jr, Becker J. W., Lipscomb W. N., Edelman G. M. Structure of soncanavalin A at 4 A resolution. Proc Natl Acad Sci U S A. 1971 Aug;68(8):1853–1857. doi: 10.1073/pnas.68.8.1853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. SRI RAM J., TAWDE S. S., PIERCE G. B., Jr, MIDGLEY A. R., Jr Preparation of antibody-ferritin conjugates for immunoelectron microscopy. J Cell Biol. 1963 Jun;17:673–675. doi: 10.1083/jcb.17.3.673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Singer S. J., Nicolson G. L. The fluid mosaic model of the structure of cell membranes. Science. 1972 Feb 18;175(4023):720–731. doi: 10.1126/science.175.4023.720. [DOI] [PubMed] [Google Scholar]
  16. Stackpole C. W., Aoki T., Boyse E. A., Old L. J., Lumley-Frank J., De Harven E. Cell surface antigens: serial sectioning of single cells as an approach to topographical analysis. Science. 1971 Apr 30;172(3982):472–474. doi: 10.1126/science.172.3982.472. [DOI] [PubMed] [Google Scholar]
  17. Unanue E. R., Perkins W. D., Karnovsky M. J. Ligand-induced movement of lymphocyte membrane macromolecules. I. Analysis by immunofluorescence and ultrastructural radioautography. J Exp Med. 1972 Oct 1;136(4):885–906. doi: 10.1084/jem.136.4.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Yariv J., Kalb A. J., Levitzki A. The interaction of concanavalin A with methyl alpha-D-glucopyranoside. Biochim Biophys Acta. 1968 Sep 3;165(2):303–305. doi: 10.1016/0304-4165(68)90063-9. [DOI] [PubMed] [Google Scholar]

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