Abstract
The correlation time for rotational diffusion (tau R) of 2,2,6,6-tetramethyl-4-piperidone-N-oxide (TEMPONE) in Chinese hamster lung (V79) cells has been measured. For these cells in an isosmotic solution at 20 degrees C, tau R = 4.18 X 10(-11) s, approximately 3.6 times greater than tau R = 1.17 X 10(-11) s in water. The relationship between tau R and viscosity was investigated in a number of glycerol-water (0-50%) and sucrose-water (20-40%) solutions and a constant Stokes-Einstein volume of 44 A3 was found for TEMPONE in solutions of less than 20% glycerol and sucrose. This gives an average shear viscosity (for rotation of a small molecule) of 0.038 poise for the cytoplasm. When nonsecular terms were used in the calculation of tau R, the activation energies for rotation of TEMPONE in the above solutions correlated well with the activation energies for shear viscosity. The viscosity increases as the cell is shrunk in hypertonic solutions. It also increases with decreasing temperature with an activation energy of 3.7 kcal/mol, about the same as the activation energy for the viscosity of pure water. The rotational correlation times were carefully calculated considering inhomogeneous line broadening, non-Lorentzian line shapes, the need for accurate tensor values and nonsecular terms.
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- Berg S. P., Lusczakoski D. M., Morse P. D., 2nd Spin label motion in the internal aqueous compartment of spinach thylakoids. Arch Biochem Biophys. 1979 Apr 15;194(1):138–148. doi: 10.1016/0003-9861(79)90603-9. [DOI] [PubMed] [Google Scholar]
- Burns V. W. Measurement of viscosity in living cells by a fluorescence method. Biochem Biophys Res Commun. 1969 Dec 4;37(6):1008–1014. doi: 10.1016/0006-291x(69)90232-0. [DOI] [PubMed] [Google Scholar]
- Burns V. W. Microviscosity and calcium exchange in yeast cells and effects of phenethyl alcohol. Exp Cell Res. 1971 Jan;64(1):35–40. doi: 10.1016/0014-4827(71)90189-3. [DOI] [PubMed] [Google Scholar]
- Cercek L., Cercek B. Effects of osmomolarity, calcium and magnesium ions on the structuredness of cytoplasmic matrix (SCM). Radiat Environ Biophys. 1976 Mar 30;13(1):9–12. doi: 10.1007/BF01323618. [DOI] [PubMed] [Google Scholar]
- Foster K. R., Resing H. A., Garroway A. N. Bounds on "bound water": transverse nuclear magnetic resonance relaxation in barnacle muscle. Science. 1976 Oct 15;194(4262):324–326. doi: 10.1126/science.968484. [DOI] [PubMed] [Google Scholar]
- Haak R. A., Kleinhans F. W., Ochs S. The viscosity of mammalian nerve axoplasm measured by electron spin resonance. J Physiol. 1976 Dec;263(2):115–137. doi: 10.1113/jphysiol.1976.sp011624. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keith A. D., Snipes W. Viscosity of cellular protoplasm. Science. 1974 Feb 15;183(4125):666–668. doi: 10.1126/science.183.4125.666. [DOI] [PubMed] [Google Scholar]
- Kirschner M. W. Microtubule assembly and nucleation. Int Rev Cytol. 1978;54:1–71. doi: 10.1016/s0074-7696(08)60164-3. [DOI] [PubMed] [Google Scholar]
- LEHMAN R. C., POLLARD E. DIFFUSION RATES IN DISRUPTED BACTERIAL CELLS. Biophys J. 1965 Jan;5:109–119. doi: 10.1016/s0006-3495(65)86705-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lazarides E. Intermediate filaments as mechanical integrators of cellular space. Nature. 1980 Jan 17;283(5744):249–256. doi: 10.1038/283249a0. [DOI] [PubMed] [Google Scholar]
- Lindmo T., Steen H. B. Flow cytometric measurement of the polarization of fluorescence from intracellular fluorescein in mammalian cells. Biophys J. 1977 May;18(2):173–187. doi: 10.1016/S0006-3495(77)85606-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ling G. N., Miller C., Ochsenfeld M. M. The physical state of solutes and water in living cells according to the association-induction hypothesis. Ann N Y Acad Sci. 1973 Mar 30;204:6–50. doi: 10.1111/j.1749-6632.1973.tb30770.x. [DOI] [PubMed] [Google Scholar]
- Livingston D. J., La Mar G. N., Brown W. D. Myoglobin diffusion in bovine heart muscle. Science. 1983 Apr 1;220(4592):71–73. doi: 10.1126/science.6828881. [DOI] [PubMed] [Google Scholar]
- Morse P. D., 2nd, Lusczakoski D. M., Simpson D. A. Internal microviscosity of red blood cells and hemoglobin-free resealed ghosts: a spin-label study. Biochemistry. 1979 Oct 30;18(22):5021–5029. doi: 10.1021/bi00589a033. [DOI] [PubMed] [Google Scholar]
- Morse P. D., 2nd Use of the spin label tempamine for measuring the internal viscosity of red blood cells. Biochem Biophys Res Commun. 1977 Aug 22;77(4):1486–1491. doi: 10.1016/s0006-291x(77)80146-0. [DOI] [PubMed] [Google Scholar]
- Thomas J. A., Buchsbaum R. N., Zimniak A., Racker E. Intracellular pH measurements in Ehrlich ascites tumor cells utilizing spectroscopic probes generated in situ. Biochemistry. 1979 May 29;18(11):2210–2218. doi: 10.1021/bi00578a012. [DOI] [PubMed] [Google Scholar]
- Wojcieszyn J. W., Schlegel R. A., Wu E. S., Jacobson K. A. Diffusion of injected macromolecules within the cytoplasm of living cells. Proc Natl Acad Sci U S A. 1981 Jul;78(7):4407–4410. doi: 10.1073/pnas.78.7.4407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wolosewick J. J., Porter K. R. Microtrabecular lattice of the cytoplasmic ground substance. Artifact or reality. J Cell Biol. 1979 Jul;82(1):114–139. doi: 10.1083/jcb.82.1.114. [DOI] [PMC free article] [PubMed] [Google Scholar]
