Abstract

The development of small molecules is essential to modulate the cellular functions of biological targets in living system. Target Guided Synthesis (TGS) approaches have been used for the identification of potent small molecules for biological targets. We herein demonstrate an innovative example of TGS using DNA nano-templates that promote Huisgen cycloaddition from an array of azide and alkyne fragments. A G-quadruplex and a control duplex DNA nano-template have been prepared by assembling the DNA structures on gold-coated magnetic nanoparticles. The DNA nano-templates facilitate the regioselective formation of 1,4-substituted triazole products, which are easily isolated by magnetic decantation. The G-quadruplex nano-template can be easily recovered and reused for five reaction cycles. The major triazole product, generated by the G-quadruplex inhibits c-MYC expression by directly targeting the c-MYC promoter G-quadruplex. This work highlights that the nano-TGS approach may serve as a valuable strategy to generate target-selective ligands for drug discovery.

Highlights

  • The development of small molecules is essential to modulate the cellular functions of biological targets in living system

  • We describe an azide-alkyne cycloaddition based Target Guided Synthesis (TGS) approach using c-MYC G-quadruplex and control duplex DNA monolayers assembled on gold-coated magnetic-nanoparticles as the templates

  • To develop TGS using DNA nano-templates, the thiolated DNA sequences were immobilized on the surface of gold-coated magnetic nanoparticles (Au@Fe3O4)

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Summary

Introduction

The development of small molecules is essential to modulate the cellular functions of biological targets in living system. Sharpless and co-workers developed in situ click chemistry, a kinetically controlled TGS approach in which the enzyme acetylcholinesterase was used as the target to assemble its potent small molecule inhibitors from a pool of azide and alkyne building blocks[2,3]. Small molecules identified by TGS are expected to show high binding affinity as well as specificity for the target as they are synthesized by a specific reaction in which the active site of the biological target controls the assembly of the best binding fragments. We describe an azide-alkyne cycloaddition based TGS approach using c-MYC G-quadruplex and control duplex DNA monolayers assembled on gold-coated magnetic-nanoparticles as the templates. Using biophysical and cellular assays, we establish that this compound can inhibit the c-MYC expression via G-quadruplex binding

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