Contribution of the Resonance Raman Spectroscopy to the Identification of Z DNA
- 1 June 1984
- journal article
- research article
- Published by Taylor & Francis in Journal of Biomolecular Structure and Dynamics
- Vol. 1 (6), 1335-1346
- https://doi.org/10.1080/07391102.1984.10507524
Abstract
Poly(dG-dC)•poly(dG-dC) at low salt concentration (0.1 M NaCl) and at high salt concentration (4.5 M NaCl) has been studied by Raman resonance spectroscopy using two excitation wavelengths: 257 nm and 295 nm. As resonance enhances the intensity of the lines in a proportion corresponding to the square of the molar absorption coefficient, the intensities of the lines with 295 nm wavelength excitation are enhanced about sevenfold during the B to Z transition. With 257 nm excitation wavelength the 1580 cm−1 line of guanosine is greatly enhanced in the Z form whereas with 295 nm excitation several lines are sensitive to the modifications of the conformation: the guanine band around 650 cm−1 and at 1193 cm−1 and the bands of the cytosines at 780 cm−1, 1242 cm−1 and 1268 cm−1. By comparison with the U.V. resonance Raman spectra of DNA, we conclude that resonance Raman spectroscopy allows one to characterize the B to Z transition from one line with 257 nm excitation wavelength and from three lines with 295 nm excitation. The conjoined study of these four lines should permit to observe a few base pairs being in Z form in a DNA.This publication has 24 references indexed in Scilit:
- Natural DNA sequences can form left-handed helices in low salt solution under conditions of topological constraintJournal of Molecular Biology, 1982
- Junction between Z and B conformations in a DNA restriction fragment: evaluation by Raman spectroscopy.Proceedings of the National Academy of Sciences, 1982
- The high salt form of poly(dG-dC)·poly(dG-dC) is left-handed Z-DNA: Raman spectra of crystals and solutionsNucleic Acids Research, 1981
- Left-Handed Double Helical DNA: Variations in the Backbone ConformationScience, 1981
- The tetramer d(CpGpCpG) crystallizes as a left-handed double helix.Proceedings of the National Academy of Sciences, 1980
- Left-handed DNA helicesNature, 1980
- Molecular structure of a left-handed double helical DNA fragment at atomic resolutionNature, 1979
- Polymorphism of a synthetic DNA in solutionNature, 1976
- The analysis of circular dichroism of biomoleculesProgress in Biophysics and Molecular Biology, 1973
- Salt-induced co-operative conformational change of a synthetic DNA: Equilibrium and kinetic studies with poly(dG-dC)Journal of Molecular Biology, 1972