Automated Synthesis and Purification of Guanidine‐Backbone Oligonucleotides. Issue 1 (12th June 2020)

• Record Type: Journal Article
• Authors: Skakuj, Kacper; Bujold, Katherine E.; Mirkin, Chad A.
• Editors: Beaucage, Serge L.; Bergstrom, Donald E.; Herdewijn, Piet; Matsuda, Akira
• Is Part Of: Current protocols in nucleic acid chemistry. Volume 81:Issue 1(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-06-12
• Subjects: automated oligonucleotide synthesis -- deoxynucleic guanidines (DNG) -- oligonucleotide backbone modifications -- positively charged oligonucleotides; Nucleic acids -- Laboratory manuals; Nucleic Acids -- chemical synthesis; Nucleic acids; Laboratory Manuals; Electronic books; Laboratory manuals; 572.8028
• DOI: 10.1002/cpnc.110
• Languages: English
• ISSNs: 1934-9270

Abstract

Abstract: This protocol describes a method based on iodine and a base as mild coupling reagents to synthetize deoxyribonucleic guanidines (DNGs)—oligodeoxynucleotide analogues with a guanidine backbone. DNGs display unique properties, such as high cellular uptake with low toxicity and increased stability against nuclease degradation, but have been impeded in their development by the requirement for toxic and iterative manual synthesis protocols. The novel synthesis method reported here eliminates the need for the toxic mercuric chloride and pungent thiophenol that were critical to previous DNG synthesis methods and translates their synthesis to a MerMade TM 12 automated oligonucleotide synthesizer. This method can be used to synthesize DNG strands up to 20 bases in length, along with 5′‐DNG‐DNA‐3′ chimeras, at 1‐ to 5‐μmol scales in a fully automated manner. We also present detailed and accessible instructions to adapt the MerMade TM 12 oligonucleotide synthesizer to enable the parallel synthesis of DNG and DNA/RNA oligonucleotides. Because DNG linkages alter the overall charge of the oligonucleotides, we also describe purification strategies to generate oligonucleotides with varying lengths and numbers of DNGs, based on extraction or preparative‐scale gel electrophoresis, along with methods to characterize the final products. Overall, this article provides an overview of the synthesis, purification, and handling of DNGs and mixed‐charge DNG‐DNA oligonucleotides. © 2020 Wiley Periodicals LLC. Basic Protocol 1 : Preparation of a MerMade TM synthesizer for guanidine couplings Basic Protocol 2 : Synthesis of DNG strands on a MerMade TM synthesizer Basic Protocol 3 : Purification of DNG strands using preparative acetic acid urea (AU) PAGE Basic Protocol 4 : Characterization of DNG strands using MALDI‐TOF MS Basic Protocol 5 : Characterization of DNG strands using AU PAGE Support Protocol 1 : Synthesis of initiator‐functionalized CPG Support Protocol 2 : Synthesis of thiourea monomer