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Synthesis of an End-to-End Protein–Glycopolymer Conjugate via Bio-Orthogonal Chemistry

  • Hailong Zhang
  • , Jacob Weingart
  • , Valentinas Gruzdys
  • , Xue-Long Sun
    • Cleveland State University

    Research output: Contribution to journal › Article › peer-review

    Abstract

    We report the synthesis of an end-to-end protein–glycopolymer conjugate, namely, site-specific modification of recombinant thrombomodulin at the C -terminus with a chain-end-functionalized glycopolymer. Thrombomodulin (TM) is an endothelial membrane glycoprotein that acts as a major cofactor in the protein C anticoagulant pathway. To closely mimic the glycoprotein structural feature of native TM, we proposed a site-specific glyco-engineering of recombinant TM with a glycopolymer. Briefly, recombinant TM containing the epidermal growth factor (EGF)-like domains 4, 5, and 6 (rTM 456 ) and a C -terminal azidohomoalanine was modified with a dibenzylcyclooctyne (DBCO) chain-end-functionalized glycopolymer via copper-free click chemistry to afford the end-to-end TM–glycopolymer conjugate. The TM glycoconjugation was confirmed with SDS-PAGE, Western blot, and protein C activation assay, respectively. The reported site-specific end-to-end protein glycopolymer conjugation approach facilitates uniform glycoconjugate formation via biocompatible chemistry and in high efficiency providing a rational strategy for generating an rTM-based anticoagulant agent.

    Original languageAmerican English
    JournalACS Macro Letters
    Volume5
    DOIs
    StatePublished - Jan 19 2016

    Disciplines

    • Chemistry
    • Medicinal-Pharmaceutical Chemistry

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