A Bioluminescence Resonance Energy Transfer-Based Approach for Determining Antibody-Receptor Occupancy In Vivo

被引:12
作者
Tang, Yu [1 ]
Parag-Sharma, Kshitij [2 ]
Amelio, Antonio L. [3 ,4 ]
Cao, Yanguang [1 ,4 ]
机构
[1] Univ N Carolina, Div Pharmacotherapy & Expt Therapeut, Eshelman Sch Pharm, 2318 Kerr Hall, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Grad Curriculum Cell Biol & Physiol, Biol & Biomed Sci Program, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Sch Med, Biomed Res Imaging Ctr, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Sch Med, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
关键词
1ST-IN-HUMAN CLINICAL-TRIALS; PROTEIN-PROTEIN INTERACTIONS; MONOCLONAL-ANTIBODIES; PHARMACOKINETIC MODEL; TISSUE DISTRIBUTION; DOSE SELECTION; FLOW-CYTOMETRY; BRET; BINDING; SAFETY;
D O I
10.1016/j.isci.2019.05.003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Elucidating receptor occupancy (RO) of monoclonal antibodies (mAbs) is a crucial step in characterizing the therapeutic efficacy of mAbs. However, the in vivo assessment of RO, particularly within peripheral tissues, is greatly limited by current technologies. In the present study, we developed a bioluminescence resonance energy transfer (BRET)-based systemthat leverages the large signal: noise ratio and stringent energy donor-acceptor distance dependency to measure antibody RO in a highly selective and temporal fashion. This versatile and minimally invasive system enables longitudinal monitoring of the in vivo antibody-receptor engagement over several days. As a proof of principle, we quantified cetuximab-epidermal growth factor receptor binding kinetics using this system and assessed cetuximab RO in a tumor xenograft model. Incomplete ROs were observed, even at a supra-therapeutic dose of 50 mg/kg, indicating that fractional target accessibility is achieved. The BRET-based imaging approach enables quantification of antibody in vivo RO and provides critical information required to optimize therapeutic mAb efficacy.
引用
收藏
页码:439 / +
页数:23
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