The Fluid Mosaic Model of the Structure of Cell Membranes

DOI Web Site 被引用文献228件
  • S. J. Singer
    University of California at San Diego, La Jolla
  • Garth L. Nicolson
    Armand Hammer Cancer Center of the Salk Institute for Biological Studies, La Jolla, California

書誌事項

タイトル別名
  • Cell membranes are viewed as two-dimensional solutions of oriented globular proteins and lipids.

抄録

<jats:p> A fluid mosaic model is presented for the gross organization and structure of the proteins and lipids of biological membranes. The model is consistent with the restrictions imposed by thermodynamics. In this model, the proteins that are integral to the membrane are a heterogeneous set of globular molecules, each arranged in an <jats:italic>amphipathic</jats:italic> structure, that is, with the ionic and highly polar groups protruding from the membrane into the aqueous phase, and the nonpolar groups largely buried in the hydrophobic interior of the membrane. These globular molecules are partially embedded in a matrix of phospholipid. The bulk of the phospholipid is organized as a discontinuous, fluid bilayer, although a small fraction of the lipid may interact specifically with the membrane proteins. The fluid mosaic structure is therefore formally analogous to a two-dimensional oriented solution of integral proteins (or lipoproteins) in the viscous phospholipid bilayer solvent. Recent experiments with a wide variety of techniques and several different membrane systems are described, all of which are consistent with, and add much detail to, the fluid mosaic model. It therefore seems appropriate to suggest possible mechanisms for various membrane functions and membrane-mediated phenomena in the light of the model. As examples, experimentally testable mechanisms are suggested for cell surface changes in malignant transformation, and for cooperative effects exhibited in the interactions of membranes with some specific ligands. </jats:p> <jats:p> <jats:italic>Note added in proof</jats:italic> : Since this article was written, we have obtained electron microscopic evidence that the concanavalin A binding sites on the membranes of SV40 virus-transformed mouse fibroblasts (3T3 cells) are more clustered than the sites on the membranes of normal cells, as predicted by the hypothesis represented in Fig. 7B. There has also appeared a study by Taylor <jats:italic>et al.</jats:italic> showing the remarkable effects produced on lymphocytes by the addition of antibodies directed to their surface immunoglobulin molecules. The antibodies induce a redistribution and pinocytosis of these surface immunoglobulins, so that within about 30 minutes at 37°C the surface immunoglobulins are completely swept out of the membrane. These effects do not occur, however, if the bivalent antibodies are replaced by their univalent Fab fragments or if the antibody experiments are carried out at 0°C instead of 3°C. These and related results strongly indicate that the bivalent antibodies produce an aggregation of the surface immunoglobulin molecules in the plane of the membrane, which can occur only if the immunoglobulin molecules are free to diffuse in the membrane. This aggregation then appears to trigger off the pinocytosis of the membrane components by some unknown mechanism. Such membrane transformations may be of crucial importance in the induction of an antibody response to an antigen, as well as in other processes of cell differentiation. </jats:p>

収録刊行物

  • Science

    Science 175 (4023), 720-731, 1972-02-18

    American Association for the Advancement of Science (AAAS)

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