Stellwagen N C, Stellwagen J
Department of Biochemistry, University of Iowa, Iowa City 52242.
Electrophoresis. 1989 May-Jun;10(5-6):332-44. doi: 10.1002/elps.1150100511.
Transient electric birefringence has been used as an analytical tool to study the orientation of DNA in agarose gels, and to study the orientation of the matrix alone. The sign of the birefringence of DNA oriented in an agarose gel is negative, as observed in free solution, indicating that the DNA molecules orient parallel to the direction of the electric field. If the median pore diameter of the gel is larger than the contour length of the DNA molecule, the DNA effectively does not see the matrix and the birefringence relaxation time is the same as observed in free solution. However, if the median pore diameter of the gel is smaller than the contour length of the DNA, the DNA molecule becomes stretched as well as oriented. For DNA molecules of moderate size (less than or equal to 4 kb), stretching in the gel causes the birefringence relaxation times to increase to the values expected for fully stretched molecules. Complete stretching is not observed for larger DNA molecules. The orientation and stretching of DNA molecules in the gel matrix indicates that end-on migration, or reptation, is a likely mechanism for DNA electrophoresis in agarose gels. When the electric field is rapidly reversed in polarity, very little change in the orientation of the DNA is observed if the DNA molecules were completely stretched and had reached their equilibrium orientation before the field was reversed in direction. Hence completely stretched, oriented DNA molecules are able to reverse their direction of migration in the electric field with little or no loss of orientation. However, if the DNA molecules were not completely stretched or if the equilibrium orientation had not been reached, substantial disorientation of the DNA molecules is observed at field reversal. The forced rate of disorientation in the reversing field is faster than the field-free rate of disorientation. Complicated patterns of reorientation can be observed after field reversal, depending on the degree of orientation in the original field direction. The effect of pulsed electric fields on the orientation of the agarose gel matrix itself was also investigated.(ABSTRACT TRUNCATED AT 400 WORDS)
瞬态电双折射已被用作一种分析工具,用于研究琼脂糖凝胶中DNA的取向,以及单独研究基质的取向。如在自由溶液中所观察到的那样,在琼脂糖凝胶中取向的DNA的双折射符号为负,这表明DNA分子平行于电场方向取向。如果凝胶的中值孔径大于DNA分子的轮廓长度,DNA实际上看不到基质,双折射弛豫时间与在自由溶液中观察到的相同。然而,如果凝胶的中值孔径小于DNA的轮廓长度,DNA分子会被拉伸并取向。对于中等大小(小于或等于4 kb)的DNA分子,在凝胶中的拉伸会导致双折射弛豫时间增加到完全拉伸分子预期的值。对于较大的DNA分子,未观察到完全拉伸。DNA分子在凝胶基质中的取向和拉伸表明,端对端迁移或蛇行是琼脂糖凝胶中DNA电泳的一种可能机制。当电场极性迅速反转时,如果DNA分子在电场方向反转之前已完全拉伸并达到其平衡取向,则观察到DNA的取向几乎没有变化。因此,完全拉伸、取向的DNA分子能够在电场中反转其迁移方向,而取向几乎没有损失或没有损失。然而,如果DNA分子没有完全拉伸或尚未达到平衡取向,则在电场反转时会观察到DNA分子的大量解取向。反转电场中的强制解取向速率比无电场解取向速率快。电场反转后,可以观察到复杂的重新取向模式,这取决于在原始电场方向上的取向程度。还研究了脉冲电场对琼脂糖凝胶基质本身取向的影响。(摘要截短于400字)