## Abstract The position and velocity of a band of doubleβstranded, linear DNA from bacteriophage G were measured during 120Β° pulsedβfield gel electrophoresis, using a video micrometer. Both the __x__ and __y__ coordinates were determined simultaneously in the plane of a 1% agarose gel; __x__ is th
The acceleration of linear DNA during pulsed-field gel electrophoresis
β Scribed by G. Holzwarth; Kevin J. Platt; Chad B. McKee; Richard W. Whitcomb; Glenn D. Crater
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1989
- Tongue
- English
- Weight
- 923 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0006-3525
No coin nor oath required. For personal study only.
β¦ Synopsis
The velocity and orientation of T4 and X DNA have been measured for the first 20 s during pulsed-field gel electrophoresis in order to clarify the DNA motions that occur. For a square pulse with field strength E = 10 V/cm, the velocity of X DNA increases gradually to 10.5 pm/s in 1.0 s, declines to 8.6 pm/s, and then rises to a plateau value of 9.3 pm/s after 4 s. T4 DNA behaves similarly, but more slowly. Parallel measurements of fluorescence-detected linear dichroism show that the DNA becomes substantially aligned with its chain axis parallel to the electrophoretic field E after the pulse is applied. The alignment also shows an overshoot, an undershoot, and a plateau comparable to those seen for velocity. When the field strength increases, both the velocity and the alignment reach their peaks more quickly. For all field strengths and both molecular weights, the velocity peak occurs when the molecular center of mass has moved 0.3 to 0.5 L, where L is the chain contour length. A qualitative model is provided.
π SIMILAR VOLUMES
A summary of the three main one-dimensional pulsed-field strategies (zero-integrated field, forward-biased field, and high frequency modulation) used for separating DNA molecules without band inversion within a preselected size range is given. Each of these strategies has size-specific features whic
Pulsed field gradient electrophoresis allows the separation of large DNA molecules up to 2,000 kilobases (kb) in length and has the potential to close the resolution gap between standard electrophoresis of DNA molecules (smaller than 50 kb) and standard cytogenetics (larger than 2,000 kb). We have a