Chakrabarti M C, Schwarz F P
Center for Advanced Research in Biotechnology/National Institute of Standards and Technology, 9600 Gudelsky Drive, Rockville, MD 20850, USA.
Nucleic Acids Res. 1999 Dec 15;27(24):4801-6. doi: 10.1093/nar/27.24.4801.
Thermodynamics of the thermal dissociation transitions of 10 bp PNA/DNA duplexes and their corresponding DNA/DNA duplexes in 10 mM sodium phosphate buffer (pH 7.0) were determined from differential scanning calorimetry (DSC) measurements. The PNA/DNA transition temperatures ranged from 329 to 343 K and the calorimetric transition enthalpies ranged from 209 +/- 6 to 283 +/- 37 kJ mol(-1). The corresponding DNA/DNA transition temperatures were 7-20 K lower and the transition enthalpies ranged from 72 +/- 29 to 236 +/- 24 kJ mol(-1). Agreement between the DSC and UV monitored melting (UVM) determined transition enthalpies validated analyzing the UVM transitions in terms of a two-state transition model. The transitions exhibited reversibility and were analyzed in terms of an AB = A + B two-state transition model which yielded van't Hoff enthalpies in agreement with the transition enthalpies. Extrapolation of the transition enthalpies and free energy changes to ambient temperatures yielded more negative values than those determined directly from isothermal titration calorimetry measurements on formation of the duplexes. This discrepancy was attributed to thermodynamic differences in the single-strand structures at ambient and at the transition temperatures, as indicated by UVM measurements on single DNA and PNA strands.
通过差示扫描量热法(DSC)测量,确定了10 mM磷酸钠缓冲液(pH 7.0)中10 bp的肽核酸/DNA双链体及其相应的DNA/DNA双链体的热解离转变的热力学性质。肽核酸/DNA的转变温度范围为329至343 K,量热转变焓范围为209±6至283±37 kJ mol⁻¹。相应的DNA/DNA转变温度低7至20 K,转变焓范围为72±29至236±24 kJ mol⁻¹。DSC和紫外监测熔解(UVM)测定的转变焓之间的一致性验证了根据两态转变模型分析UVM转变的合理性。这些转变具有可逆性,并根据AB = A + B两态转变模型进行分析,该模型得出的范特霍夫焓与转变焓一致。将转变焓和自由能变化外推至环境温度,得到的值比通过双链体形成的等温滴定量热法直接测定的值更负。如对单链DNA和肽核酸进行的UVM测量所示,这种差异归因于环境温度和转变温度下单链结构的热力学差异。