ORDERED PHASES IN CONCENTRATED DNA SOLUTIONS

被引:74
作者
RILL, RL [1 ]
STRZELECKA, TE [1 ]
DAVIDSON, MW [1 ]
VANWINKLE, DH [1 ]
机构
[1] FLORIDA STATE UNIV, CTR MAT RES & TECHNOL, DEPT PHYS, TALLAHASSEE, FL 32306 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0378-4371(91)90435-F
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Aqueous solutions of concentrated DNA, a strong polyelectrolyte, in 1:1 electrolyte form liquid-crystalline phases analogous to those observed for other semi-rigid neutral polymers and weak polyelectrolytes. Phase transitions were examined in detail for DNA fragments with a contour length (500 angstrom) approximating the persistence length. These fragments form at least three lyotropic phases. The lowest density or "precholesteric" phase appears to be a nematic with a slight and easily variable twist. The intermediate density phase is a true cholesteric with a pitch of almost-equal-to 2.1-mu-m. With increasing concentration the cholesteric phase unwinds prior to formation of the third, high density, columnar phase. Phase transition boundaries were determined as functions of DNA concentration from 10 to 300 mg/ml solvent, supporting electrolyte concentrations from 0.01 to 1.0 M, and temperature from 20-degrees-C to 60-degrees-C. Critical concentrations for formation of anisotropic phase (C(i)) and disappearance of isotropic phase (C(a)) were only moderately dependent on temperature. C(i), C(a), and the pitch of the cholesteric phase were surprisingly insensitive to the supporting electrolyte concentration. The insensitivity can be most simply related to the high concentrations required for anisotropic phase formation by these rather short, highly charged rod-like DNA fragments. At high concentrations the DNA counterions contribute significantly to the effective ionic strength, hence overall charge screening, and the counterion atmosphere as monitored by Na-23 NMR, appears to be perturbed by inter-rod interactions.
引用
收藏
页码:87 / 116
页数:30
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