| Electric Birefringence in Solutions of High Molecular Weight Ribonucleic Acid Biophysical Journal, Volume 7, Issue 1, 1 January 1967, Pages 13-24 E.I. Golub and V.G. Nazarenko Abstract The electric birefringence of low ionic strength solutions of high molecular weight ribonucleic acids from various sources was studied. RNA preparations with a high helical content were found to have negative electric birefringence as a result of the segment anisotropy of the helical portions of the RNA molecule. For completely unfolded molecules of RNA, the electric birefringence is positive and results from the orientation of the macromolecular coil. In intermediate cases, the observed electric birefringence is the sum of negative and positive birefringence. The negative birefringence is caused by the segment orientation of helical sections, and the positive birefringence is caused by the orientation of the macromolecular coil as a whole. Different relaxation times for the positive and negative birefringence permit the pulsed electric birefringence method to analyze these separate phenomena. Abstract | PDF (1008 kb) |
| Birefringence of Protein Solutions and Biological Systems Biophysical Journal, Volume 3, Issue 2, 1 March 1963, Pages 143-154 Edwin W. Taylor and William Cramer Abstract The intrinsic birefringences of TMV, tropocollagen, and paramyosin were calculated from flow birefringence measurements using the theory of Peterlin and Stuart. The values are -0.029, -0.029, and -0.030, respectively. The intrinsic birefringences of TMV and tropocollagen were measured as a function of the refractive index of the solvent in glycerol-water mixtures. In both cases the values were not constant and became less negative as the refractive index increased. Theoretical calculations showed that the large solvent effect could not be caused by a hydration shell of index different from that of the bulk solvent. It is concluded that either () the intrinsic birefringence calculated from the Peterlin-Stuart theory is incorrect or () the intrinsic birefringence depends markedly on the solvent. These results are of importance to the problem of quantitative polarized light microscopy since the separation of form and intrinsic birefringence contributions is based on the assumption that intrinsic birefringence is independent of solvent. Abstract | PDF (735 kb) |
| Form birefringence of muscle Biophysical Journal, Volume 56, Issue 2, 1 August 1989, Pages 401-413 R.C. Haskell, F.D. Carlson and P.S. Blank Abstract We investigate the sensitivity of measurements of muscle birefringence to cross-bridge dynamics in the resting, active, and rigor states. The theory of form birefringence is reviewed, and an optical model is constructed for the form birefringence of muscle. Values for the parameters in the model are selected or deduced from the literature. As an illustration of the use of the model, plausible distributions for the orientations of cross-bridges in the resting, active, and rigor states are constructed using a model for cross-bridge dynamics suggested by Huxley and Kress (1985). The general magnitude of the predictions of our model is comparable with that of published measurements of muscle birefringence. However, the precise values of the predicted birefringence for the resting, active, and rigor states are sensitive to the assumed orientations of cross-bridges. We also investigate the dependence of muscle birefringence on sarcomere length and on disorder in the orientation of the myofilament array. We conclude that measurements of muscle birefringence can play a useful role in distinguishing between proposed models of cross-bridge dynamics. Abstract | PDF (1249 kb) |
Copyright © 1987 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 52, Issue 2, 295-301, 1 August 1987
doi:10.1016/S0006-3495(87)83216-2
Research Article
C. Rosenblatt, P. Yager and P.E. Schoen
Francis Bitter National Magnet Laboratory, Massachusetts Institute of Technology, Cambridge 02139.
Lipid tubules, which are straight hollow cylinders consisting of lipid bilayers, are shown to orient in strong magnetic fields. Birefringence measurements were made of dilute samples of tubules of 1,2-bis(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (DC23PC) in magnetic fields of up to 4 T. The tubules were found to orient with their long axes parallel to the field direction, with saturated orientation [P2 (cos theta] approximately greater than 0.95) found at approximately 2 T. From known distributions of lengths and the number of bilayers in the walls, a value delta chi = (-7 +/- 1) X 10(-9) erg cm-3 G-2 was calculated for the tubules, which compares well with some previously reported values for phosphatidylcholines. Magnetic alignment will permit more sophisticated structural studies of monomeric and polymeric tubules, and provide a method of orienting macromolecules in the tubule walls or interior.