Macromolecules, viruses, and cells may be anisotropic with regard to light absorption in part or the whole of their structures. Anisotropies could arise as a result of a regular non-random orientation or coiling of ultraviolet-absorbing macromolecules such as DNA, RNA or protein within the organism. For example, oriented parallel fibers of DNA are known to be anisotropic at 260 mμ due to the regular orientation of the ultraviolet-absorbing purines and pyrimidines. If there is only one anisotropic part of an organism, the anisotropy may be masked by isotropic absorption in other components and may not be detected by absorption measurements with polarized light. An absorption anisotropy in an ultraviolet sensitive component could be resolved as an inactivation anisotropy for the organism (or molecule) if one were to study the biological effects of incident polarized ultraviolet. One need only make the reasonable assumption that the quantum yield for the biological effect is the same for all absorbed energy of a given wavelength and that the more energy is absorbed, the greater the biological effect. Hence incident polarized light may have a greater or less effectiveness for a given biological alteration, depending on the direction of the electric vector with regard to some axis of the organism. Although alignment of organisms would be preferred to implement this idea, many organisms of interest cannot be easily aligned. In this paper, we explore the possibilities for detecting such inactivation anisotropies by the polarized ultraviolet irradiation of an unoriented stationary collection of units. If the organisms are assumed to be randomly oriented in three dimensions but held stationary during irradiation, differences between polarized light and unpolarized fight survival curves are theoretically expected. However, the magnitude of the differences is so small as to make experimental resolution improbable with anything except unreasonably large dichroic ratios. If one axis of the organism is constrained to stay fixed in a plane, then the possibility of experimentally resolving an anisotropy is considerably improved. For dichroic ratios less than one, the best resolution is obtained from a comparison of the survival curve for the electric vector parallel to the plane of the organism axes to the survival curve for the electric vector perpendicular to that plane. For dichroic ratios > 1, the best resolution is obtained from a comparison of the survival curve for unpolarized light incident perpendicular to the plane to that for polarized light with the electric vector perpendicular to the plane. For dichroic ratios to be expected from some DNA configurations, it seems possible that this resolution is good enough to detect inactivation anisotropies.
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