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Solid-phase synthesis of protein-polymers on reversible immobilization supports

Author

Listed:
  • Hironobu Murata

    (Carnegie Mellon University)

  • Sheiliza Carmali

    (Carnegie Mellon University
    Carnegie Mellon University)

  • Stefanie L. Baker

    (Carnegie Mellon University
    Carnegie Mellon University)

  • Krzysztof Matyjaszewski

    (Carnegie Mellon University
    Carnegie Mellon University)

  • Alan J. Russell

    (Carnegie Mellon University
    Carnegie Mellon University
    Carnegie Mellon University
    Carnegie Mellon University)

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.

Suggested Citation

  • Hironobu Murata & Sheiliza Carmali & Stefanie L. Baker & Krzysztof Matyjaszewski & Alan J. Russell, 2018. "Solid-phase synthesis of protein-polymers on reversible immobilization supports," Nature Communications, Nature, vol. 9(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03153-8
    DOI: 10.1038/s41467-018-03153-8
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