| Literature DB >> 27923197 |
Li Zhou1, Hsuan-Yao Wang1, Shanshan Tong2, Curtis T Okamoto1, Wei-Chiang Shen3, Jennica L Zaro4.
Abstract
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 FcγR-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.Entities:
Keywords: Fc fusion; Human growth hormone; Pharmacodynamics; Pharmacokinetics; Protein delivery; Single chain Fc
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Year: 2016 PMID: 27923197 DOI: 10.1016/j.biomaterials.2016.11.051
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479