| Regional Biophysics Meeting 2005, March 16-20, Zreče, Slovenia | [NanoBioTech] |
We report on a study of the interactions between holes and molecular vibrations on dry DNA using photoinduced infrared absorption spectroscopy. Laser photoexcited holes are found to have a room-temperature lifetime in excess of >1 ms, clearly indicating the presence of localization. However, from a quantitative model analysis of the frequency shifts of vibrational modes caused by the holes, we find the hole-vibrational coupling constant to be relatively small, 0.2. This interaction leads to a change in the conformational energy of E0~0.015 eV, which is too small to cause self-trapping at room temperature. We conclude that, at least in the dry (A) form, DNA is best understood in terms of a double chain of coupled quantum dots arising from the pseudorandom chain sequence of base pairs, in which Anderson localization prevents the formation of a metallic state.
Email: ales.omerzu@ijs.si
Address: Department of Complex Matter, Institute Jozef Stefan, Jamova 39, 1000 Ljubljana, Slovenia