A Concise Approach to Site-Specific Topological Protein-Poly(amino acid) Conjugates Enabled by in Situ-Generated Functionalities

作者：Hou, Yingqin; Yuan, Jingsong; Zhou, Yu; Yu, Jin; Lu, Hua^*

来源：Journal of the American Chemical Society, 2016, 138(34): 10995-11000.

DOI：10.1021/jacs.6b05413

• RING-OPENING POLYMERIZATION
• NATIVE CHEMICAL LIGATION
• N-CARBOXYANHYDRIDES
• BIOLOGICAL APPLICATIONS
• RADICAL POLYMERIZATION
• PEPTIDE THIOESTERS
• BLOCK-COPOLYMERS
• PROTEIN LIGATION
• C-TERMINUS
• SORTASE

Controlling the topology of polymer-modified proteins has attracted growing interest. However, one of the main challenges in this field is the lack of efficient and site specific methods for installing multiple bioorthogonal functionalities on substrate polymers. We report here an orchestrating strategy that provides easy access to various topological protein poly(amino acid) (PAA) conjugates in high yields. This method features the in situ installation of two "chemical handles", including a thioester for native chemical ligation and a polyglycine nucleophile for sortase A-mediated ligation, at both ends of substrate PAAs. As a result, neither pre-functionalization of initiator or monomer units, nor post-polymerization modification of the resultant polymers, is necessary. Site-specific topological conjugates, particularly circular conjugates, can be conveniently synthesized under mild conditions from the functionalized PAAs. The biomedical utility of our method is demonstrated by the rapid and efficient generation of several therapeutic interferon-a conjugates, which exhibit significantly enhanced protease resistance and thermostability. Given the versatility of both PAAs and proteins, the method offers a convenient approach to producing libraries of conjugates for biological applications.

• 出版日期2016-8-31
• 单位北京大学