Abstract
A dynamic pattern generating automaton has been constructed. The rules controlling its function furnish the non-random generation of sub-patterns in consecutive cycles, within a large plane area, covered by four different classes of units of constant mean frequency in each class (standard system). The stabilization of certain specific sub-patterns over 100 subsequent cycles of pattern generation (modified systems) resulted in the modification of the frequency and frequency distribution of the sub-patterns relative to the standard system. Some new types of sub-patterns, not encountered in the standard system, also made appearance in the modified systems. The functioning of the standard and modified systems was analyzed and compared by the methods of mathematical statistics. The automaton was used to model certain features of the cytoplasmic membrane. The latter was regarded as a device by which the cell collects information about its environment. The dynamic generation of sub-patterns was taken as the cell's manner of asking questions, and the complementary chemical structures present in the environment were treated as possible answers to these. The irreversible question-answer interactions were regarded as signals and were modelled by the stabilization of specific sub-patterns. It was found that in a dynamic system like the model presented, it is not necessary to code each possible sub-pattern individually. Precise coding of the relative frequency of units per class and of their possible interactions is sufficient to furnish statistically constant mean frequencies for a given range of sub-patterns. In a dynamic system, the actual range of sub-patterns arisen in a population of identical individuals depends only on the size of the population. If the latter is appropriately large, all possible sub-patterns may be simultaneously present at any time at the average frequencies characteristic of each. Stabilized sub-patterns (signals) seem to modify specifically the frequencies of the other sub-patterns generated by the normal automaton. Some sub-patterns may disappear permanently, while others (new ones) may turn up and persist at given frequencies. Missense signals may definitively put the automaton out of order, i.e. result in the cell's complete misorientation in respect of its relations to the normal tissue structure.
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Ben-Bassat, Hannah, Polliak, S., Rosenbaum, S.M., Naparstek, E., Shouval, D., Inbar, M.: Fluidity of membrane lipids and lateral mobility of concanavallin A receptors in the cell surface of normal lymphocytes and lymphocytes from patients with malignant lymphomas and leukemias. Cancer Res. 37, 1307–1312 (1977)
Boeynaems, J.M., Dumont, J.E.: The two-step model of ligandreceptor interaction. Mol. Cell. Endocrinol. 7, 33–47 (1977a)
Boeynaems, J.M., Dumont, J.E.: Models of dissociable receptors applicable to cyclic AMP-dependent protein kinases and membrane receptors. Mol. Cell. Endocrinol. 7, 275–295 (1977b)
Braun, V., Krieger-Brauer, Heidemarie, J.: Interrelationship of the phage λ receptor protein and maltose transport in mutants of Escherichia coli K 12. Biochim. Biophys. Acta 469, 89–98 (1977)
Changeux, J.P., Blumenthal, R., Kasai, M., Podleski, T.: Confirmational transitions in the course of membrane excitation. Molecular properties of drug receptors. Ciba Foundation Symp. (1970)
Edidin, M.: Rotational and translational diffusion in membranes. Ann. Rev. Biophys. Bioeng. 3, 179–201 (1974)
Engasser, J.M., Flamm, M., Horvath, Cs.: Hormone regulation of cellular metabolism: Interplay of membrane transport and consecutive enzymatic reation. J. Theoret. Biol. 67, 433–445 (1977)
Erdmann, E.: Cell membrane receptors for cadiac glycosides in the heart. Basic. Res. Cardiol. 72, 315–325 (1977)
Finegold, L.: Cell membrane fluidity: Molecular modeling of particle aggregations seen in electron microscopy. Biochim. Biophys. Acta 448, 393–398 (1976)
Friedenberg, R., Blatt, A., Gallucci, V., Danielli, J.F., Shames, I.: Electrostatics of membrane systems. I. A non-statical approach to cellular membrane systems. J. Theoret. Biol. 11, 465–477 (1966a)
Friedenberg, R., Blatt, A.J., Gallucci, V.: Electrostatics of membrane systems. II. Fixed charge and dipole planar surfaces of finite dimensions. J. Theoret. Biol. 11, 478–484 (1966b)
Friedenberg, R., Blatt, A.J., Gallucci, V.: Electrostatics of membrane systems. III. The potential energy functions of idealized models of fixed charge and dipole distributions as related to surface chemical phenomena. J. Theoret. Biol. 11, 485–489 (1966c)
Gebhardt, C., Gruler, H., Sackmann, E.: On domain structure and local curvature in lipid bilayers and biological membranes. Z. Naturforsch. 32c, 581–596 (1977)
Gitler, C.: Plasticity of biological membranes. Ann. Rev. Biophys. Bioeng. 1, 51–92 (1972)
Green, D.E., Ji, S., Bruckner, R.F.: Structure-function unitization model of biological membranes. Bioenergetics 4, 527–558 (1972)
Gulik-Krzywicki, T.: Structural studies of the associations between biological membrane components. Biochim. Biophys. Acta 415, 1–28 (1975)
Hantke, K.: Phage T6-Colicin K. receptor and nucleoside transport in Escherichia coli. FEBS Letters 70, 109–112 (1976)
Hazelbauer, G.L.: Role of the receptor for bacteriophage lambda in the functioning of maltose chemoreceptor of Escherichia coli. J. Bacteriol. 124, 119–126 (1975)
Hoffmann, Sandra, S., Kolodny, G.M.: Insulin receptors in 3T3 fibroblasts. Exp. Cell Res. 107, 293–299 (1977)
Huang, H.W.: Mobility and diffusion in the plane of cell membrane. J. Theoret. Biol. 40, 11–17 (1973)
Israelachvili, J.N., Mitchell, D.J., Ninham, B.W.: Theory of self-assembly of hydrocarbon amphiphiles into micelles and bilayers. J. Chem. Soc. Faraday Trans. II. 72, 1525–1568 (1976)
Israelachvili, J.N.: Refinement of the fluid-mosaic model of membrane structure. Biochim. Biophys. Acta 469, 221–225 (1977)
Koch, A., Lomniczi, B., György, E.: Studies on the initial phases of poliovirus reproduction cycle. III. Action of fatty acids and Tween 80. Acta microbiol. Acad. Sci. hung. 13, 243–254 (1966)
Koch, A., Drén, Cs., György, E.: Saturated fatty acids in poliovirus host cell interaction. I. Stimulation and inhibition of virion uptake. Acta microbiol. Acad. Sci. hung. 15, 77–85 (1968)
Koch, A., György, E.: Action of cation transfer ATP-ase inhibitors on efficiency of infection with poliovirus. Acta microbiol. Acad. Sci. hung. 17, 127–131 (1970)
Koch, A.S., Fehér, G.: The possible nature of chance-event in initiation of virus infection at the cellular level. J. gen. Virol. 18, 319–327 (1973)
Koch, A.S., Fehér, G.: A theoretical treatment of the problem of virion attachment and infection of the host cell. Acta microbiol. Acad. Sci. hung. 21, 245–256 (1974)
Lucy, J.A.: Globular lipid micelles and cell membranes. J. Theoret. Biol. 7, 360–373 (1964)
Lucy, J.A.: Theoretical and experimental models for biological membranes. In: Biological membranes — Physical fact and function, pp. 233–288. Chapman, D. ed. London-New York: Academic Press 1968
Luzzati, V., Husson, F.: The structure of the liquid crystalline phases of lipid-water systems. J. Cell Biol. 12, 207–219 (1962)
Nagy, Z., Koch, A.: Saturated fatty acids in poliovirus host cell interaction. II. Model experiment on stimulation of phagocytosis. Acta microbiol. Acad. Sci. hung. 15, 87–96 (1968)
Nicolson, G.L.: Transmembrane control of the receptors on normal and tumor cells I. Biochim. Biophys. Acta 457, 57–108 (1976a)
Nicolson, G.L.: Transmembrane control of the receptors on normal and tumor cells. II. Biochim. Biophys. Acta 458, 1–72 (1976b)
O'Brien, J.S.: Cell membranes, composition, structure, function. J. theoret. Biol. 15, 307–324 (1967)
Parsegian, V.A.: Long-range physical forces in the biological milieu. Ann. Rev. Biophys. Bioeng. 2, 221–255 (1973)
Robertson, J.D.: The ultrastructure of cell membranes and their derivatives. Biochem. Soc. No. 16, 3–43 (1959)
Robertson, J.D.: Molecular structure of biological membranes. In: Handbook of Molecular Cytology, pp. 1404–1443. Lima-de-Faria, A., ed. Amsterdam: North Holland Publishing Co. 1969
Scott Jr., H.L.: A model for phase transitions in lipid bilayers and biological membranes. J. theoret. Biol. 46, 241–253 (1974)
Seshadri, M.S.: A reaction-diffusion coupled system with multiple steady states. J. theoret. Biol. 47, 351–365 (1974)
Singer, S.J., Nicolson, G.L.: The fluid mosaic model of the structure of cell membranes. Science 175, 720–731 (1972)
Szmelcman, S., Hofnung, M.: Maltose transport in Escherichia coli K-12: Involvement of the bacteriophage lambda receptor. J. Bacteriol. 124, 112–118 (1975)
Urry, D.W.: Protein conformation in biomembranes: Optical rotation and absorption of membrane suspensions. Biochim. Biophys. Acta. 265, 115–168 (1972)
Wayne, R., Neilands, J.B.: Evidence for common binding sites for ferrichrome compounds and bacteriophage Φ80 in the cell envelope of Escherichia coli. J. Bacteriol. 121, 497–503 (1975)
Weiss, L.: The mammalian tissue cell surface. Biochem. Soc. Symposia No. 22, pp. 32–50. Cambridge: University Press 1963
Willmer, E.N.: Steroids and cell surfaces. Biol. Rev. 36, 368–398 (1961)
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Reader of publications in physics, Gondolat Publishing House, Budapest, Hungary
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Koch, A.S., Fehér, G. & Lukovits, I. A simple model of dynamic receptor pattern generation. Biol. Cybernetics 32, 125–138 (1979). https://doi.org/10.1007/BF00337389
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DOI: https://doi.org/10.1007/BF00337389