Electro-Optical and Hydrodynamic Properties of Synthetic Polyribonucleotides in Solutions as Studied by Electric Birefringence
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- Masato Tanigawa
- Department of Material Science, Faculty of Science, Hiroshima University1-3-1 Kagamiyama, Higashi-Hiroshima 724
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- Kiwamu Yamaoka
- Department of Material Science, Faculty of Science, Hiroshima University1-3-1 Kagamiyama, Higashi-Hiroshima 724
抄録
<jats:title>Abstract</jats:title> <jats:p>The electro-optical and hydrodynamic properties of four synthetic polyribonucleic acids were clarified by electric birefringence methods which take the molecular-weight distribution into consideration. Parallel double-stranded helices, poly(adenylic acid)·poly(protonated adenylic acid), I, and poly(cytidylic acid)·poly(protonated cytidylic acid), II, are known to possess an electric permanent dipole moment, because the reversing-pulse electric birefringence (RPEB) signals of these duplexes exhibit dips upon pulse reversal. The RPEB signals of antiparallel double-stranded poly(adenylic acid)·poly(uridylic acid), III, and poly(guanylic acid)·poly(cytidylic acid), IV, show no dip; therefore, these polynucleotides have no permanent dipole moment. By analyzing the relaxation time of the birefringence decay signals, the axial translations of the polynucleotides per base-pair were determined to be 4.0 Å for I, 2.7 Å for III, and 2.4 Å for IV, respectively. By analyzing the dependence of the steady-state birefringence values on the electric-field strength, the magnitudes of the permanent dipole moments per unit length of I and II projected onto the helix axes were found to be ca. 0.4 debye Å−1. The electric properties unraveled by electric birefringence experiments were compared with calculations based on a recent Manning theory. An unsaturable induced dipole moment may result from the polarization of the Debye–Hückel ion-atmosphere, while a saturable induced dipole moment is probably caused by the polarization of counter ions that are condensed on the charged sites of a polyion. The experimental values deviate from calculated values at ionic strengths lower than 0.0001; hence, the Manning theory is not applicable in this region.</jats:p>
収録刊行物
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- Bulletin of the Chemical Society of Japan
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Bulletin of the Chemical Society of Japan 68 (2), 481-492, 1995-02-01
Oxford University Press (OUP)
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詳細情報 詳細情報について
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- CRID
- 1360846644034354560
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- NII論文ID
- 130004057843
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- ISSN
- 13480634
- 00092673
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