Advancing Genetic Alphabet Expansion: Synthesis of 7‐(2‐Thienyl)‐Imidazo[4,5‐b]pyridine (Ds) and 4‐(4‐Pentyne‐1,2‐diol)‐1‐Propynyl‐2‐Nitropyrrole (Diol‐Px) for Use in Replicable Unnatural Base Pairs for PCR Applications

Abstract

Expanding the genetic alphabet enhances DNA recombinant technologies by introducing unnatural base pairs (UBPs) beyond the standard A–T and G–C pairs, leading to biomaterials with novel and increased functionalities. Recent developments include UBPs that effectively function as a third base pair in replication, transcription, and/or translation processes. One such UBP, Ds–Px, demonstrates extremely high specificity in replication. Chemically synthesized DNA fragments containing Ds bases are amplified by PCR with the 5′‐triphosphates of Ds and Px deoxyribonucleosides (dDsTP and dPxTP). The Ds–Px pair system has applications in enhanced DNA data storage, generation of high‐affinity DNA aptamers, and incorporation of functional elements into RNA through transcription. This protocol describes the synthesis of the amidite derivative of Ds (dDs amidite), the triphosphate dDsTP, and the diol‐modified dPxTP (Diol‐dPxTP) for PCR amplifications involving the Ds–Px pair. © 2024 Wiley Periodicals LLC.Basic Protocol 1: Synthesis of Ds deoxyribonucleoside (dDs)Basic Protocol 2: Synthesis of dDs amiditeBasic Protocol 3: Synthesis of dDs triphosphate (dDsTP)Basic Protocol 4: Synthesis of Pn deoxyribonucleoside (4‐iodo‐dPn)Basic Protocol 5: Synthesis of acetyl‐protected diol‐modified Px deoxyribonucleoside (Diol‐dPx)Basic Protocol 6: Synthesis of Diol‐dPx triphosphate (Diol‐dPxTP)Basic Protocol 7: Purification of triphosphatesSupport Protocol 1: Synthesis of Hoffer's chlorosugarSupport Protocol 2: Preparation of 0.5 M pyrophosphate in DMFSupport Protocol 3: Preparation of 2 M TEAB buffer