Abstract
Using fast-scanning atomic force microscopy, we directly visualized the interaction of Escherichia coli RNA polymerase (RNAP) with DNA at the scan rate of 1-2 frames per second. The analyses showed that the RNAP can locate the promoter region not only by sliding but also by hopping and/or segmental transfer. Upon the addition of 0.05 mM NTPs to the stalled complex, the RNAP molecule pulled the template DNA uni-directionally at the rates of 15 nucleotides/s on average. The present method is potentially applicable to examine a variety of protein-nucleic acid interactions, especially those involved in the process of gene regulation.
| Original language | English |
|---|---|
| Pages (from-to) | 3187-3192 |
| Number of pages | 6 |
| Journal | FEBS Letters |
| Volume | 586 |
| Issue number | 19 |
| DOIs | |
| State | Published - 21 Sep 2012 |
Keywords
- Atomic force microscopy
- Fast-scanning atomic force microscopy
- Protein-DNA interaction
- RNA polymerase