Single chain Fc-dimer-human growth hormone fusion protein for improved drug delivery

被引:6
|
作者
Zhou, Li [1 ]
Wang, Hsuan-Yao [1 ]
Tong, Shanshan [1 ,2 ]
Okamoto, Curtis T. [1 ]
Shen, Wei-Chiang [1 ]
Zaro, Jennica L. [1 ,3 ]
机构
[1] Univ Southern Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, 1985 Zonal Ave, Los Angeles, CA 90089 USA
[2] Jiangsu Univ, Sch Pharm, Dept Pharmaceut, Zhenjiang, Jiangsu, Peoples R China
[3] West Coast Univ, Sch Pharm, Dept Pharmaceut Sci, 590 N Vermont Ave, Los Angeles, CA 90004 USA
关键词
Fc fusion; Single chain Fc; Protein delivery; Human growth hormone; Pharmacokinetics; Pharmacodynamics; IGG TRANSPORT; NEONATAL MALNUTRITION; STRUCTURAL INSIGHTS; RECEPTOR FCRN; GAMMA-RI; THERAPEUTICS; PEPTIDE; BINDING; DESIGN; PHARMACOKINETICS;
D O I
10.1016/j.biomaterials.2016.11.051
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Fc fusion protein technology has been successfully used to generate long-acting forms of several protein therapeutics. In this study, a novel Fc-based drug carrier, single chain Fc-dimer (sc(Fc)(2)), was designed to contain two Fc domains recombinantly linked via a flexible linker. Since the Fc dimeric structure is maintained through the flexible linker, the hinge region was omitted to further stabilize it against proteolysis and reduce FcyR-related effector functions. The resultant sc(Fc)(2) candidate preserved the neonatal Fc receptor (FcRn) binding. sc(Fc)(2)-mediated delivery was then evaluated using a therapeutic protein with a short plasma half-life, human growth hormone (hGH), as the protein drug cargo. This novel carrier protein showed a prolonged in vivo half-life and increased hGH-mediated bioactivity compared to the traditional Fc-based drug carrier. sc(Fc)(2) technology has the potential to greatly advance and expand the use of Fc-technology for improving the pharmacokinetics and bioactivity of protein therapeutics. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:24 / 31
页数:8
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