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. 1982 Sep;39(3):273–278. doi: 10.1016/S0006-3495(82)84517-7

Temperature dependence of the yield shear resultant and the plastic viscosity coefficient of erythrocyte membrane. Implications about molecular events during membrane failure.

R E Waugh
PMCID: PMC1328944  PMID: 7139026

Abstract

Structural failure of the erythrocyte membrane in shear deformation occurs when the maximum shear resultant (force/length) exceeds a critical value, the yield shear resultant. When the yield shear resultant is exceeded, the membrane flows with a rate of deformation characterized by the plastic viscosity coefficient. The temperature dependence of the yield shear resultant and the plastic viscosity coefficient have been measured over the temperature range 10-40 degrees C. Over this range the yield shear resultant does not change significantly (+/- 15%), but the plastic viscosity coefficient changes exponentially from a value of 1.3 X 10(-2) surface poise (dyn s/cm) at 10 degrees C to a value of 6.2 X 10(-4) surface poise (SP) at 40 degrees C. The different temperature dependence of these two parameters is not surprising, inasmuch as they characterize different molecular events. The yield shear resultant depends on the number and strength of intermolecular connections within the membrane skeleton, whereas the plastic viscosity depends on the frictional interactions between molecular segments as they move past one another in the flowing surface. From the temperature dependence of the plastic viscosity, a temperature-viscosity coefficient, E, can be calculated: eta p = constant X exp(--E/RT). This quantity (E) is related to the probability that a molecular segment can "jump" to its next location in the flowing network. The temperature-viscosity coefficient for erythrocyte membrane above the elastic limit is calculated to be 18 kcal/mol, which is similar to coefficients for other polymeric materials.

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Selected References

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  1. Brenner S. L., Korn E. D. Spectrin/actin complex isolated from sheep erythrocytes accelerates actin polymerization by simple nucleation. Evidence for oligomeric actin in the erythrocyte cytoskeleton. J Biol Chem. 1980 Feb 25;255(4):1670–1676. [PubMed] [Google Scholar]
  2. Evans E. A., Hochmuth R. M. Membrane viscoplastic flow. Biophys J. 1976 Jan;16(1):13–26. doi: 10.1016/S0006-3495(76)85659-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Fairbanks G., Steck T. L., Wallach D. F. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971 Jun 22;10(13):2606–2617. doi: 10.1021/bi00789a030. [DOI] [PubMed] [Google Scholar]
  4. Gratzer W. B. The red cell membrane and its cytoskeleton. Biochem J. 1981 Jul 15;198(1):1–8. doi: 10.1042/bj1980001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hochmuth R. M., Buxbaum K. L., Evans E. A. Temperature dependence of the viscoelastic recovery of red cell membrane. Biophys J. 1980 Jan;29(1):177–182. doi: 10.1016/S0006-3495(80)85124-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hochmuth R. M., Evans E. A., Colvard D. F. Viscosity of human red cell membrane in plastic flow. Microvasc Res. 1976 Mar;11(2):155–159. doi: 10.1016/0026-2862(76)90047-9. [DOI] [PubMed] [Google Scholar]
  7. Hochmuth R. M., Mohandas N., Blackshear P. L., Jr Measurement of the elastic modulus for red cell membrane using a fluid mechanical technique. Biophys J. 1973 Aug;13(8):747–762. doi: 10.1016/S0006-3495(73)86021-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Lux S. E. Dissecting the red cell membrane skeleton. Nature. 1979 Oct 11;281(5731):426–429. doi: 10.1038/281426a0. [DOI] [PubMed] [Google Scholar]
  9. Shotton D. M., Burke B. E., Branton D. The molecular structure of human erythrocyte spectrin. Biophysical and electron microscopic studies. J Mol Biol. 1979 Jun 25;131(2):303–329. doi: 10.1016/0022-2836(79)90078-0. [DOI] [PubMed] [Google Scholar]
  10. Ungewickell E., Bennett P. M., Calvert R., Ohanian V., Gratzer W. B. In vitro formation of a complex between cytoskeletal proteins of the human erythrocyte. Nature. 1979 Aug 30;280(5725):811–814. doi: 10.1038/280811a0. [DOI] [PubMed] [Google Scholar]
  11. Ungewickell E., Gratzer W. Self-association of human spectrin. A thermodynamic and kinetic study. Eur J Biochem. 1978 Aug 1;88(2):379–385. doi: 10.1111/j.1432-1033.1978.tb12459.x. [DOI] [PubMed] [Google Scholar]
  12. Waugh R. E. Surface viscosity measurements from large bilayer vesicle tether formation. I. Analysis. Biophys J. 1982 Apr;38(1):19–27. doi: 10.1016/S0006-3495(82)84526-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Waugh R., Evans E. A. Thermoelasticity of red blood cell membrane. Biophys J. 1979 Apr;26(1):115–131. doi: 10.1016/S0006-3495(79)85239-X. [DOI] [PMC free article] [PubMed] [Google Scholar]

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