A Switchable Site-Specific Antibody Conjugate

被引:13
作者
Lyu, Zhigang [1 ]
Kang, Lei [2 ,3 ,4 ]
Buuh, Zakey Yusuf [1 ]
Jiang, Dawei [3 ,4 ,5 ]
McGuth, Jeffrey C. [1 ]
Du, Juanjuan [6 ]
Wissler, Haley L. [1 ]
Cai, Weibo [3 ,4 ]
Wang, Rongsheng E. [1 ]
机构
[1] Temple Univ, Dept Chem, 1901 N 13th St, Philadelphia, PA 19122 USA
[2] Peking Univ, Dept Nucl Med, Hosp 1, Beijing 100034, Peoples R China
[3] Univ Wisconsin, Dept Radiol, Madison, WI 53705 USA
[4] Univ Wisconsin, Dept Med Phys, Madison, WI 53705 USA
[5] Shenzhen Univ, Sch Biomed Engn, Hlth Sci Ctr, Guangdong Key Lab Biomed Measurements & Ultrasoun, Shenzhen 518060, Peoples R China
[6] Tsinghua Univ, Sch Pharmaceut Sci, Beijing 100084, Peoples R China
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
UNNATURAL AMINO-ACIDS; DRUG CONJUGATE; IMMUNO-PCR; CANCER;
D O I
10.1021/acschembio.8b00107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genetic incorporation of unnatural amino acids (UAAs) provides a unique approach to the synthesis of site-specific antibody conjugates that are homogeneous and better defined constructs than random conjugates. Yet, the yield varies for every antibody, and the process is costly and time-consuming. We have developed a switchable alpha GCN4-Fab conjugate that incorporates UAA p-acetylphenylalanine. The GCN4 peptide is used as a switch, and antibodies fused by GCN4 can direct the alpha GCN4-Fab conjugate to target different cancer cells for diagnosis, imaging, or therapeutic treatment. More importantly, this switchable conjugate demonstrated an impressive potential for pretargeted imaging in vivo. This approach illustrates the utility of an orthogonal switch as a general strategy to endow versatility to a single antibody conjugate, which should facilitate the application of UAA-based site -specific conjugates for a host of biomedical uses in the future.
引用
收藏
页码:958 / 964
页数:7
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