Šinkevičiūtė Ugnė, Sanchez-Quirante Tania, Rožánková Samanta, Poštová Slavětínská Lenka, Raindlová Veronika, Hocek Michal
Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Flemingovo nam. 2, CZ-16610, Prague 6, Czech Republic.
Department of Organic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, CZ-12843, Prague 2, Czech Republic.
Chembiochem. 2025 Jun 16;26(12):e202500241. doi: 10.1002/cbic.202500241. Epub 2025 May 21.
A series of adenosine triphosphate (ATP) derivatives bearing chloro, fluoro, amino, methyl, vinyl, and ethynyl groups at position 2 are synthesized and tested as substrates for RNA and DNA polymerases. The modified nucleotides work well in in vitro transcription with T7 RNA polymerase and primer extension (PEX) using engineered DNA polymerases (TGK, 2M) except for the bulkier 2-vinyl- and 2-ethynyl-ATP derivatives that give truncated products. However, in single nucleotide incorporation followed by PEX, they still can be used for site-specific incorporation of reactive modifications into RNA that can be further used for postsynthetic labeling through thiol-ene or Cu-catalyzed alkyne-azide cycloadditions reactions. All modified ATPs work in polyadenylation catalyzed by poly(A) polymerase to form long 3'-polyA tails containing the modifications that also can be used for labeling.
合成了一系列在2位带有氯、氟、氨基、甲基、乙烯基和乙炔基的三磷酸腺苷(ATP)衍生物,并作为RNA和DNA聚合酶的底物进行测试。除了体积较大的2-乙烯基-和2-乙炔基-ATP衍生物会产生截短产物外,这些修饰的核苷酸在使用工程化DNA聚合酶(TGK、2M)进行的T7 RNA聚合酶体外转录和引物延伸(PEX)中表现良好。然而,在单核苷酸掺入后进行PEX时,它们仍可用于将反应性修饰位点特异性掺入RNA中,进而通过硫醇-烯或铜催化的炔-叠氮环加成反应用于合成后标记。所有修饰的ATP在聚(A)聚合酶催化的聚腺苷酸化反应中起作用,形成含有可用于标记的修饰的长3'-聚A尾巴。