Protein PEPylation: A New Paradigm of Protein-Polymer Conjugation

被引:80
作者
Hou, Yingqin [1 ]
Lu, Hua [1 ]
机构
[1] Peking Univ, Beijing Natl Lab Mol Sci, Key Lab Polymer Chem & Phys,Minist Educ, Coll Chem & Mol Engn,Ctr Soft Matter Sci & Engn, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
RING-OPENING POLYMERIZATION; ACCELERATED BLOOD CLEARANCE; ANTI-PEG IGM; INTERFERON-ALPHA CONJUGATE; ACID N-CARBOXYANHYDRIDES; IN-SITU GROWTH; VIVO HALF-LIFE; SYNTHETIC POLYPEPTIDES; IMMUNOLOGICAL-PROPERTIES; TREHALOSE GLYCOPOLYMERS;
D O I
10.1021/acs.bioconjchem.9b00236
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Various polymers have been tested for protein conjugation with a goal of bridging the complementary advantages of both components. However, many of these polymers, including the most well-established PEG, are nondegradable, which raises potential concerns on their cumulative chronic toxicity. Moreover, the immunogenicity of PEG has recently evoked considerable controversy. Synthetic polypeptides, on the other hand, are biomimetic polymers with tunable degradability, versatile side chain functionalities, unique secondary structures, and fascinating self-assembly behaviors. These properties have made them promising materials in protein modification for various applications. In this Topical Review, we summarize recent advances and list a number of interesting future directions in protein polypeptide conjugation, which we termed protein PEPylation.
引用
收藏
页码:1604 / 1616
页数:13
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