Mouse Monoclonal Antibodies Against Human c-Mpl and Characterization for Flow Cytometry Applications

被引:11
作者
Abbott, Christina [2 ]
Huang, Guo [1 ]
Ellison, Aaron R. [2 ]
Chen, Ching [2 ]
Arora, Taruna [2 ]
Szilvassy, Stephen J. [1 ]
Wei, Ping [1 ]
机构
[1] Amgen Inc, Dept Hematol & Oncol, Thousand Oaks, CA 91320 USA
[2] Amgen Inc, Dept Prot Sci, Thousand Oaks, CA 91320 USA
来源
HYBRIDOMA | 2010年 / 29卷 / 02期
关键词
PLATELET PRODUCTION; RECEPTOR MPL; THROMBOPOIETIN; MEGAKARYOCYTOPOIESIS; EXPRESSION; BINDING; GROWTH; MECHANISMS; BIOLOGY; LIGAND;
D O I
10.1089/hyb.2009.0095
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mouse monoclonal antibodies (MAbs) against human c-Mpl, the cognate receptor for thrombopoietin (TPO), were generated using hybridoma technology and characterized by various assays to demonstrate their specificity and affinity. Two such MAbs, 1.6 and 1.75, were determined to be superior for flow cytometry studies and exhibited double-digit picomolar (pM) affinities to soluble human c-Mpl protein. Both MAbs specifically bound to cells engineered to overexpress human c-Mpl protein, immortalized human hematopoietic cell lines that express endogenous c-Mpl, primary human bone marrow and peripheral blood-derived CD34(+) cells, and purified human platelets. No binding was detected on cell lines that did not express c-Mpl. Receptor competition and siRNA knock-down studies further confirmed the specificity of antibodies 1.6 and 1.75 for human c-Mpl. In contrast to these newly generated MAbs, none of eight commercially available anti-c-Mpl antibodies tested were found to bind specifically to human c-Mpl and were thus shown to be unsuitable for flow cytometry studies. Monoclonal antibodies 1.6 and 1.75 will therefore be useful flow cytometry reagents to detect cell surface c-Mpl expression.
引用
收藏
页码:103 / 113
页数:11
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