Marky L A, Canuel L, Jones R A, Breslauer K J
Biophys Chem. 1981 Apr;13(2):141-9. doi: 10.1016/0301-4622(81)80013-0.
Differential scanning calorimetry and temperature-dependent uv spectroscopy are used to thermodynamically characterize the double-strand to single-strand transition of the self-complementary deoxyribo-oligonucleotide ATGCAT. The calorimetric experiments provide a value of 33.6 kcal (mol of double strand)-1 for the transition between 10 and 90 degree C. In conjunction with available temperature-dependent nmr data (which reveals terminal base pair fraying), we attempt to define specifically those interactions to which the calorimetrically measured enthalpy change refers. Values of delta HV.H. (van 't Hoff enthalpy change) are derived from the spectroscopic and calorimetric data and compared with the delta H obtained directly from the calorimetric experiment. This comparison reveals that the part of the thermally-induced transition that occurs between 10 and 90 degree C is well represented by a two-state process. It is noted that is assessing the applicability of the two-state model it is best to compare the delta with delta HV.H. Hcal. obtained from the calorimetric rather than the spectroscopic data.
差示扫描量热法和温度依赖紫外光谱法被用于从热力学角度表征自互补脱氧核糖寡核苷酸ATGCAT的双链到单链的转变。量热实验给出了10至90摄氏度之间转变的焓变为33.6千卡/(摩尔双链)。结合现有的温度依赖核磁共振数据(该数据揭示了末端碱基对的解链),我们试图明确量热法测量的焓变所涉及的具体相互作用。从光谱和量热数据中得出范特霍夫焓变(delta HV.H.)的值,并与直接从量热实验获得的delta H进行比较。这种比较表明,在10至90摄氏度之间发生的热诱导转变部分可以很好地用两态过程来描述。需要注意的是,在评估两态模型的适用性时,最好将delta与从量热数据而非光谱数据获得的delta HV.H.和Hcal进行比较。