Zwitterionic Peptide Cloak Mimics Protein Surfaces for Protein Protection

被引:52
作者
Yuan, Zhefan [1 ,2 ]
Li, Bowen [2 ]
Niu, Liqian [1 ,2 ]
Tang, Chenjue [3 ]
McMullen, Patrick [1 ,2 ]
Jain, Priyesh [1 ,2 ]
He, Yuwei [1 ,2 ,4 ,5 ]
Jiang, Shaoyi [1 ,2 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
[3] Univ Washington, Dept Mat Sci & Engn, Seattle, WA 98195 USA
[4] Fudan Univ, Sch Pharm, Dept Pharmaceut, Shanghai 201203, Peoples R China
[5] Minist Educ, Key Lab Smart Drug Delivery, Shanghai 201203, Peoples R China
基金
美国国家卫生研究院;
关键词
asparaginase; EK peptide; immunogenicity; protein conjugate; zwitterion; HYDROPHOBIC INTERACTION CHROMATOGRAPHY; IMAGING MASS-SPECTROMETRY; POLYETHYLENE-GLYCOL; NONSPECIFIC INTERACTIONS; HALF-LIFE; PEGYLATION; PEG; IMMUNOGENICITY; ANTIBODY; BIOPHARMACEUTICALS;
D O I
10.1002/anie.202004995
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Inspired by the amino acid composition of natural protein surfaces, we developed a zwitterionic cloak containing multi-layers of short alternating glutamic acid and lysine (EK) peptides as a facile, highly effective and low-immunogenicity approach for the protection and delivery of biotherapeutics. Each EK layer grafted to proteins provides multiple times of new lysine reaction sites for the growth of subsequent EK layers. This unique design allows EK peptides to achieve high coating density on proteins, overcoming the limitation of traditional conjugation strategies that rely on the number of innate lysine groups. A triple-layer EK cloak manifests to successfully eliminate the specific and non-specific interactions of protected asparaginase with biological media while prolong the drug circulation time and significantly mitigate its immunogenicity in vivo, suggesting an EK peptide cloak as a promising approach to improve the safety and efficacy of biotherapeutics.
引用
收藏
页码:22378 / 22381
页数:4
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