DNA-Catalyzed DNA Cleavage by a Radical Pathway with Well-Defined Products

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• 作者：Yujeong Lee ; Paul C. Klauser ; Benjamin M. Brandsen ; Cong Zhou ; Xinyi Li ; Scott K. Silverman
• 刊名：Journal of the American Chemical Society
• 出版年：2017
• 出版时间：January 11, 2017
• 年：2017
• 卷：139
• 期：1
• 页码：255-261
• 全文大小：535K
• ISSN：1520-5126

文摘

We describe an unprecedented DNA-catalyzed DNA cleavage process in which a radical-based reaction pathway cleanly results in excision of most atoms of a specific guanosine nucleoside. Two new deoxyribozymes (DNA enzymes) were identified by in vitro selection from N₄₀ or N₁₀₀ random pools initially seeking amide bond hydrolysis, although they both cleave simple single-stranded DNA oligonucleotides. Each deoxyribozyme generates both superoxide (O₂^–• or HOO^•) and hydrogen peroxide (H₂O₂) and leads to the same set of products (3′-phosphoglycolate, 5′-phosphate, and base propenal) as formed by the natural product bleomycin, with product assignments by mass spectrometry and colorimetric assay. We infer the same mechanistic pathway, involving formation of the C4′ radical of the guanosine nucleoside that is subsequently excised. Consistent with a radical pathway, glutathione fully suppresses catalysis. Conversely, adding either superoxide or H₂O₂ from the outset strongly enhances catalysis. The mechanism of generation and involvement of superoxide and H₂O₂ by the deoxyribozymes is not yet defined. The deoxyribozymes do not require redox-active metal ions and function with a combination of Zn²⁺ and Mg²⁺, although including Mn²⁺ increases the activity, and Mn²⁺ alone also supports catalysis. In contrast to all of these observations, unrelated DNA-catalyzed radical DNA cleavage reactions require redox-active metals and lead to mixtures of products. This study reports an intriguing example of a well-defined, DNA-catalyzed, radical reaction process that cleaves single-stranded DNA and requires only redox-inactive metal ions.