Anderson D M, Folk W R
Biochemistry. 1976 Mar 9;15(5):1022-30. doi: 10.1021/bi00650a012.
Iodination of DNA by the reaction originally described by S. L. Commerford ((1971), Biochemistry 10, 1993) is extremely sensitive to the secondary structure of the DNA. Cytidines in denatured simian virus 40 (SV40) DNA react at a slightly slower rate than free cytidine monophosphate; hydrogen-bonded cytidines in SV40 form I DNA are iodinated considerably more slowly; elimination of the negative supercoils in form I DNA by conversion to form II or form III reduces reactivity even further. The residual reactivity of form II or form III duplex DNA is not due to preferential iodination of unpaired cytidines near phosphodiester bond breaks; rather iodination occurs throughout the molecule. Cytidine monophosphate has been used as a model for DNA, to enable spectral measurements of its reaction with iodine and T1C13. At temperatures above 42 degrees C and at pH 5.0, formation of 5-iodocytidine is limited by the rate of formation of an intermediate, probably 5-iodo-6-hydroxydihydrocytidine. At lower temperatures, the conversion of intermediate to product is rate limiting, but can be accelerated by lowering the pH. By appropriate adjustment of pH, or temperature, the formation of intermediate or its conversion to product can be accelerated. Iodination destabilizes the DNA duplex. Iodocytosines in SV40 DNA are preferentially removed by S1 nuclease. Heavily iodinated DNA does not reassociate normally, but DNA with only 5-10% of its cytosines iodinated appears to reassociate with normal kinetics, if duplex formation is measured by hydroxylapatite chromatography. Conditions are described to permit preparation of DNA, which reassociates normally, having a specific activity of 10(8) cpm/mug.
S. L. 康默福德最初描述的反应((1971),《生物化学》10, 1993)对DNA的二级结构极为敏感。变性的猴病毒40(SV40)DNA中的胞嘧啶反应速率略低于游离的胞嘧啶单磷酸;SV40 I型DNA中形成氢键的胞嘧啶碘化速度要慢得多;通过转化为II型或III型消除I型DNA中的负超螺旋会进一步降低反应活性。II型或III型双链DNA的残余反应活性并非由于磷酸二酯键断裂附近未配对胞嘧啶的优先碘化;相反,碘化发生在整个分子中。胞嘧啶单磷酸已被用作DNA的模型,以便对其与碘和三氯化铊的反应进行光谱测量。在42摄氏度以上的温度和pH值为5.0时,5-碘胞嘧啶的形成受中间体(可能是5-碘-6-羟基二氢胞嘧啶)形成速率的限制。在较低温度下,中间体向产物的转化是限速步骤,但可以通过降低pH值来加速。通过适当调节pH值或温度,可以加速中间体的形成或其向产物的转化。碘化会使DNA双链不稳定。SV40 DNA中的碘胞嘧啶优先被S1核酸酶去除。高度碘化的DNA不能正常复性,但如果通过羟基磷灰石柱层析测量双链的形成,只有5-10%的胞嘧啶被碘化的DNA似乎能以正常动力学复性。文中描述了允许制备具有10(8) cpm/μg比活度且能正常复性的DNA的条件。