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Furan Oxidation Cross-Linking: A New Approach for the Study and Targeting of Peptide/Protein and Nucleic Acid Interactions

机译:呋喃氧化交联:一种新方法,用于研究肽/蛋白质和核酸相互作用的研究和靶向

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A novel mildly inducible cross-linking methodology for DNA interstrand cross-linking (ICL) was developed by our group, inspired by the metabolic activation of furan moieties (Figure 1). Nucleosides, modified in various ways with furan and easily accessible due to the stability and wide commercial availability of furan derivatives, are incorporated into oligonucleotides (ODNs). After hybridization into a duplex they are oxidized to a very reactive ketobutenal, resulting in selective and high yielding cross-link formation with the opposite base [1]. The strategy has now been investigated for broader application, as the method further holds potential for cross-linking of DNA binding proteins to their target.
机译:对DNA Interstrand交联(ICL)的新型轻微诱导的交联方法由我们的组开发,受到呋喃部分的代谢活化的启发(图1)。核苷,以各种方式改性呋喃,并且由于呋喃衍生物的稳定性和广泛的商业可用性而易于获得,掺入寡核苷酸(ODN)中。在将双链体杂交后,它们被氧化成非常反应性的酮丁烯,导致选择性和高产生的交联形成,其具有相对的基础[1]。该策略现已调查进行更广泛的应用,因为该方法进一步拥有DNA结合蛋白对其靶标的潜力。

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