Department of Biochemical and Chemical Engineering, Chair for Bioprocess Engineering, TU Dortmund University E, mil-Figge-Strasse 66, 44227, Dortmund, Germany.
Department of Biochemical and Chemical Engineering, Laboratory of Technical Biology, TU Dortmund University, Emil-Figge-Strasse 66, 44227, Dortmund, Germany.
Chembiochem. 2020 Nov 16;21(22):3225-3228. doi: 10.1002/cbic.202000433. Epub 2020 Aug 4.
Cyclic GMP-AMP synthase (cGAS) is a cytosolic DNA sensor that catalyzes the synthesis of the cyclic GMP-AMP dinucleotide 2'3'-cGAMP. 2'3'-cGAMP functions as inducer for the production of type I interferons. Derivatives of this important second messenger are highly valuable for pharmaceutical applications. However, the production of these analogues requires complex, multistep syntheses. Herein, human cGAS is shown to react with a series of unnatural nucleotides, thus leading to novel cyclic dinucleotides. Most substrate derivatives with modifications at the nucleobase, ribose, and the α-thio phosphate were accepted. These results demonstrate the catalytic promiscuity of human cGAS and its utility for the biocatalytic synthesis of cyclic dinucleotide derivatives.
环鸟苷酸-腺苷酸合酶(cGAS)是一种胞质 DNA 传感器,可催化环鸟苷酸-腺苷酸二核苷酸 2'3'-cGAMP 的合成。2'3'-cGAMP 作为 I 型干扰素产生的诱导剂。这种重要的第二信使的衍生物在药物应用中非常有价值。然而,这些类似物的生产需要复杂的多步合成。本文显示人 cGAS 与一系列非天然核苷酸反应,从而导致新型的环二核苷酸的产生。大多数在碱基、核糖和α-硫代磷酸部分修饰的底物衍生物都被接受。这些结果表明人 cGAS 的催化混杂性及其在环二核苷酸衍生物的生物催化合成中的用途。