Babkina Olga V, Chutko Catherine A, Shashkov Alexander A, Dzhidzhoev Murat S, Eritja Ramon I, Gromova Elizaveta S
Department of Chemistry and Belozersky Institute of Physical and Chemical Biology, Moscow State University, Moscow 119992, Russia.
Photochem Photobiol Sci. 2002 Sep;1(9):636-40. doi: 10.1039/b202028a.
We used a XeCl excimer laser with 50 ns pulses, a frequency of 0.3 Hz and a wavelength of 308 nm in appropriate conditions for the photocrosslinking of EcoRII restriction endonuclease to a 14-mer DNA duplex, containing a 5-iodo-2'-deoxyuridine residue (IdU). IdU replaced the thymidine residue within the EcoRII recognition sequence 5'-CCT/AGG. The binding of EcoRII endonuclease to the IdU-containing DNA duplex was analyzed by gel retardation assay in the presence of Ca2+ or Mg2+ ions. Photocrosslinking of EcoRII to the IdU-containing DNA duplex occurred in a pre-reactive complex formed in the presence of Ca2+ ions. Photocrosslinking yields as a function of time and UV-laser light intensity were studied.
在合适的条件下,我们使用了一台XeCl准分子激光器,其脉冲宽度为50纳秒,频率为0.3赫兹,波长为308纳米,用于将EcoRII限制性内切酶光交联到一个含有5-碘-2'-脱氧尿苷残基(IdU)的14聚体DNA双链体上。IdU取代了EcoRII识别序列5'-CCT/AGG中的胸腺嘧啶残基。在Ca2+或Mg2+离子存在的情况下,通过凝胶阻滞试验分析了EcoRII内切酶与含IdU的DNA双链体的结合。EcoRII与含IdU的DNA双链体的光交联发生在Ca2+离子存在下形成的预反应复合物中。研究了光交联产率与时间和紫外激光光强的函数关系。