Correlation of binary polyolefin phase behavior with statistical segment length asymmetry

1992 ◽  
Vol 25 (20) ◽  
pp. 5547-5550 ◽  
Author(s):  
Frank S. Bates ◽  
Mark F. Schulz ◽  
Jeffrey H. Rosedale ◽  
Kristoffer Almdal

2018 ◽  
Vol 140 (2) ◽  
Author(s):  
Kevin D. Dorfman

The development of bright bisintercalating dyes for deoxyribonucleic acid (DNA) in the 1990s, most notably YOYO-1, revolutionized the field of polymer physics in the ensuing years. These dyes, in conjunction with modern molecular biology techniques, permit the facile observation of polymer dynamics via fluorescence microscopy and thus direct tests of different theories of polymer dynamics. At the same time, they have played a key role in advancing an emerging next-generation method known as genome mapping in nanochannels. The effect of intercalation on the bending energy of DNA as embodied by a change in its statistical segment length (or, alternatively, its persistence length) has been the subject of significant controversy. The precise value of the statistical segment length is critical for the proper interpretation of polymer physics experiments and controls the phenomena underlying the aforementioned genomics technology. In this perspective, we briefly review the model of DNA as a wormlike chain and a trio of methods (light scattering, optical or magnetic tweezers, and atomic force microscopy (AFM)) that have been used to determine the statistical segment length of DNA. We then outline the disagreement in the literature over the role of bisintercalation on the bending energy of DNA, and how a multiscale biomechanical approach could provide an important model for this scientifically and technologically relevant problem.



1995 ◽  
Vol 273 (7) ◽  
pp. 626-632 ◽  
Author(s):  
A. Dondos ◽  
G. Staikos




Polymer ◽  
1998 ◽  
Vol 39 (17) ◽  
pp. 4155-4158 ◽  
Author(s):  
C. Gans ◽  
J. Schnee ◽  
U. Scherf ◽  
G. Staikos ◽  
E. Pierri ◽  
...  


1993 ◽  
Vol 26 (20) ◽  
pp. 5457-5460 ◽  
Author(s):  
J. K. Kallitsis ◽  
K. Gravalos ◽  
A. Dondos


Author(s):  
E. Naranjo

Equilibrium vesicles, those which are the stable form of aggregation and form spontaneously on mixing surfactant with water, have never been demonstrated in single component bilayers and only rarely in lipid or surfactant mixtures. Designing a simple and general method for producing spontaneous and stable vesicles depends on a better understanding of the thermodynamics of aggregation, the interplay of intermolecular forces in surfactants, and an efficient way of doing structural characterization in dynamic systems.



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