Yasar Selcuk, Podgornik Rudolf, Valle-Orero Jessica, Johnson Mark R, Parsegian V Adrian
Department of Physics, University of Massachusetts, Amherst, MA 01003, United States.
1] Department of Physics, University of Massachusetts, Amherst, MA 01003, United States [2] Department of Theoretical Physics, J. Stefan Institute, SI-1000 Ljubljana, Slovenia [3] Department of Physics, Faculty of Mathematics and Physics, University of Ljubljana, SI-1000 Ljubljana, Slovenia.
Sci Rep. 2014 Nov 5;4:6877. doi: 10.1038/srep06877.
A new method of finely temperature-tuning osmotic pressure allows one to identify the cholesteric → line hexatic transition of oriented or unoriented long-fragment DNA bundles in monovalent salt solutions as first order, with a small but finite volume discontinuity. This transition is similar to the osmotic pressure-induced expanded → condensed DNA transition in polyvalent salt solutions at small enough polyvalent salt concentrations. Therefore there exists a continuity of states between the two. This finding, together with the corresponding empirical equation of state, effectively relates the phase diagram of DNA solutions for monovalent salts to that for polyvalent salts and sheds some light on the complicated interactions between DNA molecules at high densities.
一种精确调节渗透压的新方法,能够让人们将一价盐溶液中取向或未取向的长片段DNA束的胆甾相→线六方相转变识别为一级转变,具有小但有限的体积不连续性。这种转变类似于在足够低的多价盐浓度下,多价盐溶液中渗透压诱导的伸展态→凝聚态DNA转变。因此两者之间存在状态的连续性。这一发现,连同相应的经验状态方程,有效地将一价盐DNA溶液的相图与多价盐的相图联系起来,并为高密度下DNA分子间复杂的相互作用提供了一些线索。