A Bioorthogonal Small Molecule Selective Polymeric "Clickase".
Junfeng ChenKe LiSarah E BonsonSteven C ZimmermanPublished in: Journal of the American Chemical Society (2020)
Synthetic polymer scaffolds may serve as gatekeepers preventing the adhesion of biomacromolecules. Herein, we use gating to develop a copper-containing single-chain nanoparticle (SCNP) catalyst as an artificial "clickase" that operates selectively on small molecules that are able to penetrate the polymeric shell. Whereas the analogous clickase with surface ammonium groups performs highly efficient copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) reactions on both alkynylated proteins and small molecule substrates, the new SCNP clickase with polyethylene glycol (PEG) groups is only active on small molecules. Further, the new SCNP resists uptake by cells allowing extracellular click chemistry to be performed. We describe two proof of principle applications that illustrate the utility of the bioorthogonal activity. First, the SCNP catalyst is able to screen for ligands that bind proteins, including proteolysis targeting chimera (PROTAC)-like molecules. Second, the nonmembrane permeable SCNP can efficiently catalyze the click reaction extracellularly, thereby enabling in situ anticancer drug synthesis and screening without the catalyst perturbing intracellular functions.
Keyphrases
- highly efficient
- small molecule
- drug delivery
- cancer therapy
- protein protein
- room temperature
- induced apoptosis
- ionic liquid
- drug release
- cell cycle arrest
- oxide nanoparticles
- cell death
- reactive oxygen species
- reduced graphene oxide
- pseudomonas aeruginosa
- emergency department
- oxidative stress
- metal organic framework
- carbon dioxide
- adverse drug
- cystic fibrosis
- drug discovery
- signaling pathway
- electron transfer
- cell adhesion
- visible light