Abstract
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 Å) 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 ≈2.1 μm. 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 concentration from 0.01 to 1.0 M, and temperature from 20°C to 60°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 23Na NMR, appears to be perturbed by inter-rod interactions.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Physica A: Statistical Mechanics and its Applications
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.