Abstract

Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds. Full access to abiotic/biotic synthetic diversity first occurred when chemistry was developed to grow nucleic acids and peptides from reversibly immobilized precursors. Protein–polymer conjugates, however, have always been synthesized in solution in multi-step, multi-day processes that couple innovative chemistry with challenging purification. Here we report the generation of protein–polymer hybrids synthesized by protein-ATRP on reversible immobilization supports (PARIS). We utilized modified agarose beads to covalently and reversibly couple to proteins in amino-specific reactions. We then modified reversibly immobilized proteins with protein-reactive ATRP initiators and, after ATRP, we released and analyzed the protein polymers. The activity and stability of PARIS-synthesized and solution-synthesized conjugates demonstrated that PARIS was an effective, rapid, and simple method to generate protein–polymer conjugates. Automation of PARIS significantly reduced synthesis/purification timelines, thereby opening a path to changing how to generate protein–polymer conjugates.

Highlights

  • Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds

  • In order to develop broadly applicable and predictable protein-atomtransfer radical polymerization (ATRP) on reversible immobilization supports (PARIS) syntheses of protein–polymer conjugates, we searched for a covalent and reversible coupling chemistry that could be used with almost any protein

  • Dialkyl maleic anhydrides covalently react with primary amines above pH

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Summary

Introduction

Facile automated biomacromolecule synthesis is at the heart of blending synthetic and biologic worlds. Conjugate Dh and polymer molecular weight increased with increasing monomer concentration for both PARIS and solution-based conjugate synthesis (each maintaining low PDIs)

Results
Conclusion
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