Synthesis of 2-Substituted Adenosine Triphosphate Derivatives and their use in Enzymatic Synthesis and Postsynthetic Labelling of RNA.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChemBioChem Pub Date : 2025-05-02 DOI:10.1002/cbic.202500241
Ugnė Šinkevičiūtė, Tania Sanchez-Quirante, Samanta Rožánková, Lenka Poštová Slavětínská, Veronika Raindlová, Michal Hocek
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引用次数: 0

Abstract

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.

2-取代ATP衍生物的合成及其在酶促合成和RNA合成后标记中的应用。
合成了一系列三磷酸腺苷衍生物,在2位上含有氯、氟、氨基、甲基、乙烯基和乙基,并作为RNA和DNA聚合酶的底物进行了测试。除了体积较大的2-乙烯基和2-乙基atp衍生物会产生截短的产物外,修饰的核苷酸在T7聚合酶和引物延伸(PEX)使用工程DNA聚合酶(TGK, 2M)的体外转录中表现良好。然而,在单核苷酸掺入和PEX之后,它们仍然可以用于特异性位点的反应修饰掺入RNA中,这些修饰可以通过巯基或CuAAC反应进一步用于合成后标记。所有修饰的atp都在聚(A)聚合酶(ScPAP)催化的聚腺苷化中起作用,形成含有修饰的长3'-聚A尾部,也可用于标记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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