Hocek Michal, Fojta Miroslav
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Gilead & IOCB Research Center, Flemingovo nam. 2, CZ-16610 Prague 6, Czech Republic.
Org Biomol Chem. 2008 Jul 7;6(13):2233-41. doi: 10.1039/b803664k. Epub 2008 Apr 2.
Construction of functionalized nucleic acids (DNA or RNA) via polymerase incorporation of modified nucleoside triphosphates is reviewed and selected applications of the modified nucleic acids are highlighted. The classical multistep approach for the synthesis of modified NTPs by triphosphorylation of modified nucleosides is compared to the novel approach consisting of direct aqueous cross-coupling reactions of unprotected halogenated nucleoside triphosphates. The combination of cross-coupling of NTPs with polymerase incorporation gives an efficient and straightforward two-step synthesis of modified nucleic acids. Primer extension using biotinylated templates followed by separation using streptavidine-coated magnetic beads and DNA duplex denaturation is used for preparation of modified single stranded oligonucleotides. Examples of using this approach for electrochemical DNA labelling and bioanalytical applications are given.
综述了通过聚合酶掺入修饰的核苷三磷酸构建功能化核酸(DNA或RNA)的方法,并重点介绍了修饰核酸的一些选定应用。将通过修饰核苷的三磷酸化合成修饰NTP的经典多步方法与由未保护的卤代核苷三磷酸的直接水相交叉偶联反应组成的新方法进行了比较。NTP的交叉偶联与聚合酶掺入相结合,可高效、直接地两步合成修饰核酸。使用生物素化模板进行引物延伸,然后使用链霉亲和素包被的磁珠进行分离和DNA双链变性,用于制备修饰的单链寡核苷酸。给出了将该方法用于电化学DNA标记和生物分析应用的实例。