| Literature DB >> 27104806 |
Yao-Yun Fan1, Lindsay B Avery1, Mengmeng Wang1, Denise M O'Hara1, Sheldon Leung1, Hendrik Neubert1.
Abstract
The neonatal Fc receptor (FcRn) is a homeostatic receptor responsible for prolonging immunoglobulin G (IgG) half-life by protecting it from lysosomal degradation and recycling it to systemic circulation. Tissue-specific FcRn expression is a critical parameter in physiologically-based pharmacokinetic (PBPK) modeling for translational pharmacokinetics of Fc-containing biotherapeutics. Using online peptide immuno-affinity chromatography coupled with high resolution mass spectrometry, we established a quantitative FcRn tissue protein expression profile in human FcRn (hFcRn) transgenic mice, Tg32 homozygous and hemizygous strains. The concentration of hFcRn across 14 tissues ranged from 3.5 to 111.2 pmole per gram of tissue. Our hFcRn quantification data from Tg32 mice will enable a more refined PBPK model to improve the accuracy of human PK predictions for Fc-containing biotherapeutics.Entities:
Keywords: Antibody; IA-LC-HRMS; PBPK models; Tg32; human FcRn; tissue-based target quantification; transgenic mice
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Year: 2016 PMID: 27104806 PMCID: PMC4968098 DOI: 10.1080/19420862.2016.1178436
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857