On the Stability of Double Stranded Nucleic Acids
We present the first pressure-versus-temperature phase diagram for the helix-to-coil transition of double stranded nucleic acids. The thermodynamic stability of a nucleic acid duplex is a complex function of temperature and pressure and strongly depends on the denaturation temperature, T M, of the d...
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Veröffentlicht in: | Journal of the American Chemical Society 2001-09, Vol.123 (38), p.9254-9259 |
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Sprache: | eng |
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Zusammenfassung: | We present the first pressure-versus-temperature phase diagram for the helix-to-coil transition of double stranded nucleic acids. The thermodynamic stability of a nucleic acid duplex is a complex function of temperature and pressure and strongly depends on the denaturation temperature, T M, of the duplex at atmospheric pressure. Depending upon T M, pressure, and temperature, the phase diagram shows that pressure may stabilize, destabilize, or have no effect on the conformational state of DNA. To verify the phase diagram, we have conducted high-pressure UV melting experiments on poly(dIdC)poly(dIdC), a DNA duplex, poly(rA)poly(rU), an RNA duplex, and poly(dA)poly(rU), a DNA/RNA hybrid duplex. The T M values of these duplexes have been modulated by altering the solution ionic strength. Significantly, at low salt, these three duplexes have helix-to-coil transition temperatures of 50 °C or less. In agreement with the derived phase diagram, we found that the polymeric duplexes were destabilized by pressure if the T M is < ∼50 °C. However, these duplexes were stabilized by pressure if the T M is > ∼50 °C. The DNA/RNA hybrid duplex, poly(dA)poly(rU), with a T M of 31 °C in 20 mM NaCl undergoes a pressure-induced helix-to-coil transition at room temperature. This is the first report of pressure-induced denaturation of a nucleic acid duplex and provides new insights into the molecular forces stabilizing these structures. |
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ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/ja004309u |